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Hypoxia-inducible factors and the prevention of acute organ injury


Hypoxic preconditioning has long been considered as organ-protective, and its clinical usage has been suggested in elective procedures, such as coronary surgery and organ transplantation. Although the mechanisms have not been clearly elucidated, it has been postulated that changes in cell-membrane composition and upregulation of various cellular protective mechanisms are responsible for a better tolerance of acute injury. Remote preconditioning (i.e., hypoxic stress in one organ conferring resistance to acute hypoxia in other organs) suggests organ cross-talk, perhaps mediated by cytokines and the immune system.

Increased expression of heme-oxygenase (HO)-1, heat-shock proteins (HSP), growth factors such as vascular endothelial factor (VEGF), and erythropoietin (EPO) are among the numerous adaptive responses to sublethal injury that are believed to participate in tissue tolerance during subsequent stress. EPO, for instance, is a ubiquitous pleiotropic survival and growth factor that attenuates experimental acute injury in various organ systems, including neuronal, retinal, cardiac, renal, and hepatic tissues. Its clinical efficacy, though suggested in critically ill patients, is yet to be defined [1].

The expression of these protective mediators and many others is regulated by hypoxia-sensing mechanisms through the induction and stabilization of so called hypoxia-inducible factors (HIF) [2]. In this chapter, we will outline the control and action of HIF as key regulators of hypoxic adaptive response, and particularly examine HIF expression during hypoxic stress. We shall discuss recently developed measures that enable HIF signal modification and describe their potential use in conferring tissue tolerance during incipient organ injury.

HIF regulation and action

HIFs are heterodimers (Figure 1), composed of a constitutive β-subunit (HIF-β) and one of three different oxygen-dependent and transcriptionally active α-subunits, among which HIF-1α and -2α are acknowledged as promotors of hypoxia adaptation, whereas the role of HIF-3α remains unclear. Under normoxia, HIF-α subunits are constantly produced, but not allowed to accumulate, since they are rapidly hydroxylated by oxygen-dependent HIF prolyl-4-hydroxylase domain enzymes (PHD), subsequently captured by the ubiquitin ligase Von-Hippel-Lindau protein (VHL), and degraded by the proteasome. Under oxygen deficiency, PHD activity is reduced, HIF-α accumulates within the cytosol, αβ-dimers are formed, translocate into the nucleus, and bind to hypoxia response elements (HREs) in the promoter enhancer region of genes, which are subsequently transactivated [24].

Figure 1
figure 1

A schematic display of hypoxia-inducible factor (HIF) regulation and biological action. Prolyl-4 hydroxylases (PHDs) serve as oxygen sensors and under normoxic conditions promote degradation of HIF-α isoforms in the proteasome following binding with the ubiquitin ligase, Von-Hippel-Lindau protein (VHL). Hypoxia inhibits PHDs and leads to HIF-α accumulation with HIF-β, and the αβ heterodimer translocates into the nucleus, binds with hypoxia-response elements (HRE) and activates numerous genes important in cell metabolism, proliferation and survival. Many of these genes play a central role in injury tolerance and promotion of tissue oxygenation, such as erythropoietin (EPO), vascular endothelial growth factor (VEGF), inducible NO synthase (iNOS), heme oxygenase (HO)-1, glucose transporter-1, or carbonic anhydrase (CA)-9. Underscored is the inactivation of the HIF-HRE axis by hypoxia, which can be mimicked by carbon monoxide (functional anemia) or by transition metals like cobaltous chloride. Hypoxia-mimetic PHD inhibitors (PHD-I) are potent newly developed measures in the induction of the HIF-HRE axis. For simplicity, numerous additional factors involved in HIF regulation and action are not included in this cartoon and the reader is referred to comprehensive reviews such as references [3, 12].

The biological effects of the more than 100 acknowledged HIF target genes are multiple, and include key steps in cell metabolism and survival. Many of the HIF-target genes constitute a reasonable adaptation to hypoxia, such as erythropoiesis (EPO), increased glucose uptake (glucose transporter-1), switch of metabolism to glycolysis (several key enzymes of glycolysis), increased lactate utilization (lactate dehydrogenase), angiogenesis (VEGF), vasodilation (inducible nitric oxide synthase [iNOS]), removal of protons (carbonic anhydrase 9), and scavenging of free radicals (HO-1) [24].

Biological and rherapeutic modes of HIF activation

Every cell type has the potential to upregulate HIF, principally by the inhibition of PHD, under conditions when cellular oxygen demand exceeds oxygen supply, namely under cellular hypoxia. However, the threshold and extent of HIF activation may depend on the hypoxic stimulus and cell type involved. To some extent, these cellular variations may reflect different expression of various PHD isoforms in different tissues [57].

As HIF stimulation may potentiate hypoxia tolerance, studies were conducted to explore its clinical application. Widespread experimental hypoxic stimuli are listed in Table 1, all acting principally by the control of HIF-α degradation, initiated by PHDs. Except for carbon monoxide exposure, which is currently being tested in patients, none of these stimuli seems suitable for preconditional HIF activation in humans.

Table 1 Modes of HIF signal enhancement

Apart from hypoxic stabilization, widely proven in vivo, HIF activation has also been demonstrated to occur under normal ambient oxygen tensions, mostly in cell cultures challenged with cytokines and growth factors. However, under stress, oxygen demand likely is increased, thus possibly leading to intracellular hypoxia even in cells kept under room air. For technical reasons, it is probably impossible to rule out such local cellular hypoxia that may exist predominantly within the mitochondria. Beyond this academic distinction between true cellular hypoxia and normoxia, it is important to recognize that clinical conditions, like inflammation, infection and sepsis, may lead to HIF activation. Thus, theoretically, cytokines or growth factors could be used for preconditional HIF activation in humans.

Although not a reasonable therapeutic intervention, strong and stable normoxic HIF activation can be achieved by deletion of the VHL gene, which is a constant phenomenon in Von Hippel Lindau Disease and in renal clear cell carcinoma, and is also encountered in other tumors. Transgenic animals with VHL knockout serve to test the potential of HIF activation in ischemic/hypoxic diseases (C Rosenberger, unpublished data) [8]. Additional experimental probes for enhancing HIF signal are by transfection with PHD siRNA [9] or with the generation of constitutively active HIF-α transgenes [10].

So-called hypoxia mimetics block PHD activity, thus upregulating HIF under normoxia. PHDs require 2-oxoglutarate and ferrous iron as co-substrates. Non-specific PHD inhibitors are either 2-oxoglutarate analogues or interfere with Fe2+. Recently, more specific PHD inhibitors (PHD) have been synthesized [11], and are currently being tested in animal and human studies.

Figure 1 represents a simplistic scheme of the canonical HIF regulation and action. Recent discoveries underscore a host of additional compound biological pathways, associated with the regulation of the HIF signal, including the control of HIF synthesis, HIF controlling PHD synthesis, putative competing/intervening impacts of HIF-3α and PHD-3, cross-talk of HIF and other key regulators of gene expression (STAT, p-300 and others), further modification of HIF-α activity at the level of DNA hypoxia-responsive elements by small ubiquitin-like modifiers (SUMO) and factor inhibiting HIF (FIH), and the effect of reactive oxygen species (ROS), NO and Krebs cycle metabolites on HIF degradation. These complex pathways are beyond the scope of this review, and the interested reader is referred to additional references [3, 5, 1218].

HIF expression under hypoxic stress and tissue injury

The kidney serves as an excellent example for under-standing HIF expression under hypoxic stress. Renal oxygenation is very heterogeneous, with PO2 falling to levels as low as 25 mmHg in the outer medulla under normal physiologic conditions and to even lower values in the papilla [3, 4, 19]. Changes in renal parenchymal microcirculation and oxygenation have been thoroughly investigated in acute and chronic renal disorders [19, 20]. Finally, the complex renal anatomy in which different cell types are in close proximity to regions with comparable ambient oxygenation, enables comparisons of cellular HIF response.

Interestingly, HIF expression is below detection thresh-old by immunostaining in the renal medulla, despite low physiologic ambient oxygenation (It should be emphasized that this statement regarding negative HIF immunostaining in the normally hypoxic medulla relates to kidneys perfusion-fixed in vivo without an interruption of renal oxygenation before fixation. Other modes of tissue harvesting for HIF determination, either by immunostaining or by molecular biology techniques may be falsely positive, as hypoxia-induced inhibition of PHD activity is instantaneous, and may lead to HIF-α stabilization even over short periods of hypoxia). Conceivably, this reflects the plasticity of HIF control to adjust for 'physiologically normal' oxygenation (i.e., adjusted rates of HIF-α generation and degradation under normal conditions.

Enhanced renal HIF-α is noted in rodents subjected to hypoxia or to inhaled carbon monoxide (chemical hypoxia) [21], and in hypoxic isolated perfused kidneys [22]. Different cells express diverse HIF isoforms: Whereas tubular segments express HIF-1α, HIF-2α is principally produced by vascular endothelial and interstitial cells [2123]. Interestingly, HIF-dependent genes are also selectively expressed in different cell types. For instance HIF-2-triggered EPO generation is specifically found in interstitial cells in the deep cortex [24]. In hypoxic isolated perfused kidneys, attenuation of severe medullary hypoxia by the inhibition of tubular transport markedly enhanced HIF expression, probably under-scoring a window of opportunity to generate HIF and HIF-mediated adaptive responses only under moderate and sublethal hypoxic stress [22]. This pattern is consistent with HIF expression at the border of renal infarct zones only, indicating that dying cells within the critically ischemic region are incapable of mounting a hypoxia adaptive response [25].

We also found that HIF-α isoforms are stabilized in acute hypoxic stress, predominantly in the cortex in rhabdomyolysis-induced kidney injury [26], in the outer stripe of the outer medulla following ischemia and reperfusion [27, 28], or in the inner stripe and inner medulla following the induction of distal tubular hypoxic injury by radiocontrast agent, or after the inhibition of prostaglandin or NO synthesis or with their combinations [23]. Outer medullary HIF stabilization is also noted in chronic tubulointerstitial disease [29] and in experimental diabetes [30], again spatially distributed in areas with proven hypoxia. HIF was also detected in biopsies from transplanted kidneys [31]. Thus, HIF immunostaining is chronologically and spatially distributed in renal regions with abnormally low PO2.

Normal mice subjected to warm ischemia and reperfusion display limited injury only, as compared with extensive damage in HIF (+/-) mice [32]. Thus, the importance of mounting an HIF response during hypoxic stress is undeniable.

Hypoxia-driven HIF stabilization during hypoxic stress has been encountered in other organs as well. HIF-1α and PHD-2 expression increased in the neonatal rat brain following hypoxia [33] and HIF was detected in the hypoxic subendocardium [34] and in the ischemic liver [27]. HIF is also found within hypoxic regions in tumors, and may play an important role in tumor progression via upregulation of growth promoting and angiogenic factors [35].

Potential usage of HIF modulation in clinical practice

The impact of HIF stimulation on the expression of HIF-dependent tissue-protective genes led to the expectation that timely upstream HIF stimulation may have great potential in the protection of endangered organs by downstream induction of protective genes [12]. Indeed, repeated systemic hypoxia, for instance, results in enhanced expression of renal HIF and HIF-dependent genes and attenuates warm-ischemic injury [36].

The use of hypoxia-mimetic PHD inhibitors is a promising potential new treatment option in diseases such as myocardial infarction, stroke, renal or liver injury, peripheral vascular disease, or severe anemia. Studies with PHD inhibitors and other manipulations of HIF upregulation favor this hypothesis [11].


Specific PHD inhibitors induce HIF-2α expression in interstitial fibroblasts in the deep cortex [24], enhance erythropoietin generation, and were found to provoke erythrocytosis in primates [37]. Phase 2 clinical trials in patients with chronic kidney disease are currently under way, studying the effect of oral PHD inhibitors as potential substitutes to EPO injection.

Acute kidney injury

The potential protective impact of HIF upregulation by PHD inhibitors has been extensively studied in acute kidney injury. In isolated kidneys perfused with low-oxygen containing medium, pre-treatment with a PHD inhibitor improved renal blood flow and attenuated medullary hypoxic damage [38]. Conditional inactivation of VHL in mice (hence HIF stabilization) resulted in tolerance to renal ischemia and reperfusion [8] and to rhabdomyolysis-induced acute kidney injury (Rosen-berger C, unpublished data). Whereas gene transfer of negative-dominant HIF led to severe damage in the normally hypoxic renal medulla in intact rats, transfer of constitutively active HIF (HIF/VP16) induced expression of various HIF-regulated genes and protected the medulla against acute ischemic insults [39]. Furthermore, in rats and mice subjected to warm ischemia and reflow, PHD inhibitors and carbon monoxide pre-treatment (i.e., functional anemia) markedly attenuated kidney damage and dysfunction [32, 40]. Donor pre-treatment with a PHD inhibitor also prevented graft injury and prolonged survival in an allogenic kidney transplant model in rats [41]. Finally, rats preconditioned by carbon monoxide, displayed reduced cisplatin renal toxicity, with attenuation of renal dysfunction and the extent of tubular apoptosis and necrosis [42]. Taken together, all these observations indicate that HIF stabilization seemingly is a promising novel interventional strategy in acute kidney injuries [12].

Myocardial injury

Activation of the HIF system has also been found to be cardioprotective. In a model of myocardial ischemia in rabbits, pre-treatment with a PHD inhibitor induced robust expression of HO-1 and markedly attenuated infarct size and myocardial inflammation [43]. In another report, PHD inhibitors did not reduce infarct size, but improved left ventricular function and prevented remodeling [44]. In the same fashion, selective silencing of PHD-2 with siRNA 24 h before global myocardial ischemia/reperfusion in mice reduced the infarct size by 70% and markedly improved left ventricular systolic function [9]. Remote preconditioning by intermittent renal artery occlusion also resulted in cardiac protection, conceivably through PHD inhibition [45].

Enhanced levels of PHD-3 were traced in the hibernating myocardium [34] and in end-stage heart failure in humans, associated also with elevated HIF-3α [46] (which may act as a competitive inhibitor of active HIF-α isoforms [14]). Thus, PHD inhibitors may conceivably also be beneficial in these disorders. Finally, cardioprotection during heat acclimation is also mediated in part by HIF upregulation [47], providing another potential situation for the administration of PHD inhibitors.

Neuronal injuries

The effect of PHD inhibitors has also been assessed in disorders of the central nervous system. In vitro, rotenone-induced neuronal apoptosis was attenuated and autophagy increased, as the result of enhanced HIF following deferoxamine administration [48]. In vivo, PHD inhibitors have shown promising results in the attenuation of ischemic stroke [49], and might be neuroprotective in metabolic chronic neurodegenerative conditions [50]. However, studies showing inhibition of PHD-1 by ROS suggest non-HIF-mediated neuronal protection under normoxic conditions [51].

Lung injury

Preterm lambs developing respiratory distress syndrome display upregulation of PHDs with a reciprocal fall in HIF-α isoforms and HIF-dependent VEGF [53]. This observation implies that PHD inhibitors might have therapeutic potential in this clinical setup.

Liver disease

Hepatic HIF-1α is upregulated following warm ischemia [27], and is required for restoration of gluconeogenesis in the regenerating liver [52], implying yet another potential use for PHD inhibitors in acute liver disease.

Peripheral vascular disease

In a model of limb ischemia in mice, PHD inhibitors enhanced HIF expression and downstream VEGF and VEGF-receptor Flk-1, leading to improved capillary density, indicating a potential therapeutic use of PHD inhibitors in promoting angiogenesis in ischemic diseases, such as severe peripheral vascular disease [54]. Transfection with HIF-1α, combined with PHD inhibitor-treated bone marrow-derived angiogenic cells increased perfusion, motor function, and limb salvage in old mice with ischemic hind limbs [55]. Results of a phase-1 study in patients with critical limb ischemia indicate that transfection with a constitutively active form of HIF-1α might also promote limb salvage [10]. Further clinical trials with PHD inhibitors are currently under way in burn wound healing and salvage of critically ischemic limbs.

Oxidative stress

Enhanced cellular ROS concentrations, as happens with shock and tissue hypoxia, result in increased PHD activity, and this effect is antagonized by ROS scavengers [15]. This situation may lead to HIF de-stabilization and inadequate HIF response to hypoxia. For example, hypoxia-mediated HIF expression in the diabetic renal medulla is substantially improved by the administration of the membrane-permeable superoxide dismutase mimetic tempol [30]. It is, therefore, tempting to assume that ROS scavengers, as well as PHD inhibitors may improve tissue adaptive responses to hypoxia, coupled with oxidative stress. However, contradicting evidence exists, indicating that ROS might trigger HIF in the absence of hypoxia. This has been suggested by studying liver tissue in acetaminophen-induced liver injury, before the development of overt liver injury and hypoxia [56], and in aged well-fed animals [57]. The role of HIF stimulation during oxidative stress therefore needs further assessment.

Important considerations

HIF stimulation is not all-protective. The wide range of HIF-dependent genes, and its tight cross-communication with other key regulators of gene expression [13, 58, 59] raise concern regarding concomitant non-selective activation of protective as well as harmful systems. Among potential unwanted outcomes is the enhancement of tumor growth [60], promotion of fibrosis [61] or the induction of pre-eclampsia in pregnant women [62]. Indeed, whereas HIF activation is considered renoprotective in acute kidney injury, it may play a role in the progression of chronic kidney disease and certainly is an important factor in the promotion of renal malignancy [3, 20].

Diverse characteristics and distribution patterns of different PHDs [57] and particular actions of various PHD inhibitors [11, 37] might enable selective manipulation of the HIF system in a more desired way, selectively favoring advantageous HIF-dependent responses in preferred tissues. Furthermore, it is believed that activation of adverse responses requires protracted HIF stimulation, whereas short-term and transient HIF activation might suffice to activate tissue-protective systems without continuing induction of harmful systems. However, this concept needs confirmation in clinical trials.


Elucidating the mechanisms involved in HIF-mediated cellular responses to acute hypoxic stress has led to the discovery of novel potential therapeutic options for the prevention or attenuation of tissue injury. The non-selective enhancement of gene expression by current modes of HIF augmentation warrants caution, since undesired enhancement of certain genes may be hazardous.

We anticipate that in the coming years the use of PHD inhibitors and other stimulants of the HIF system will be tested in many clinical scenarios associated with critical care and emergency medicine, while HIF silencing strategies may be tested in chronic diseases, such as malignancies and disorders with enhanced tissue scarring.





factor inhibiting HIF


hypoxia-inducible factors




hypoxia response elements


heat-shock proteins


prolyl-4-hyrdoxylase domain enzymes


reactive oxygen species


small ubiquitin-like modifiers


vascular endothelial growth factor


Von-Hippel-Lindau protein.


  1. Bernhardt WM, Eckardt KU: Physiological basis for the use of erythropoietin in critically ill patients at risk for acute kidney injury. Curr Opin Crit Care 2008, 14: 621-626. 10.1097/MCC.0b013e328317ee82

    Article  PubMed  Google Scholar 

  2. Semenza G: Signal transduction to hypoxia-inducible factor 1. Biochem Pharmacol 2002, 64: 993-998. 10.1016/S0006-2952(02)01168-1

    Article  CAS  PubMed  Google Scholar 

  3. Gunaratnam L, Bonventre JV: HIF in kidney disease and development. J Am Soc Nephrol 2009, 20: 1877-1887. 10.1681/ASN.2008070804

    Article  CAS  PubMed  Google Scholar 

  4. Rosenberger C, Rosen S, Heyman S: Current understanding of HIF in renal disease. Kidney Blood Press Res 2005, 28: 325-340. 10.1159/000090187

    Article  PubMed  Google Scholar 

  5. Willam C, Maxwell PH, Nichols L, et al.: HIF prolyl hydroxylases in the rat; organ distribution and changes in expression following hypoxia and coronary artery ligation. J Mol Cell Cardiol 2006, 41: 68-77. 10.1016/j.yjmcc.2006.04.009

    Article  CAS  PubMed  Google Scholar 

  6. Li N, Yi F, Sundy CM, et al.: Expression and actions of HIF prolyl-4-hydroxylase in the rat kidneys. Am J Physiol Renal Physiol 2007, 292: F207-F216. 10.1152/ajprenal.00457.2005

    Article  CAS  PubMed  Google Scholar 

  7. Schodel J, Klanke B, Weidemann A, et al.: HIF-prolyl hydroxylases in the rat kidney: physiologic expression patterns and regulation in acute kidney injury. Am J Pathol 2009, 174: 1663-1674. 10.2353/ajpath.2009.080687

    Article  PubMed Central  PubMed  Google Scholar 

  8. Iguchi M, Kakinuma Y, Kurabayashi A, et al.: Acute inactivation of the VHL gene contributes to protective effects of ischemic preconditioning in the mouse kidney. Nephron Exp Nephrol 2008, 110: e82-e90. 10.1159/000166994

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  9. Natarajan R, Salloum FN, Fisher BJ, Kukreja RC, Fowler AA III: HIF-1 activation by prolyl 4-hyroxylase-2 gene silencing attenuates myocardial ischemia-reperfusion injury. Circ Res 2006, 98: 133-140. 10.1161/01.RES.0000197816.63513.27

    Article  CAS  PubMed  Google Scholar 

  10. Rajagopalan S, Olin J, Deitcher S, et al.: Use of a constitutively active hypoxia-inducible factor-1alpha transgene as a therapeutic strategy in no-option critical limb ischemia patients: phase I dose-escalation experience. Circulation 2007, 115: 1234-1243.

    CAS  PubMed  Google Scholar 

  11. Myllyharju J: HIF prolyl 4-hydroxylases and their potential as drug targets. Curr Pharm Des 2009, 15: 3878-3885. 10.2174/138161209789649457

    Article  CAS  PubMed  Google Scholar 

  12. Nangaku M: Novel therapeutic approach targeting the HIF-HRE system in the kidney. Adv Exp Med Biol 2009, 645: 81-86. full_text

    Article  CAS  PubMed  Google Scholar 

  13. Webb JD, Coleman ML, Pugh CW: Hypoxia, hypoxia-inducible factors (HIF), HIF hydroxylases and oxygen sensing. Cell Mol Life Sci 2009, 66: 3539-3554. 10.1007/s00018-009-0147-7

    Article  CAS  PubMed  Google Scholar 

  14. Tanaka T, Wiesener M, Bernhardt W, Eckardt KU, Warnecke C: The human HIF (hypoxia-inducible factor)-3alpha gene is a HIF-1 target gene and may modulate hypoxic gene induction. Biochem J 2009, 424: 143-151. 10.1042/BJ20090120

    Article  CAS  PubMed  Google Scholar 

  15. Callapina M, Zhou J, Schmid T, Kohl R, Brune B: NO restores HIF-1 alpha hydroxylation during hypoxia: role of reactive oxygen species. Free Radic Biol Med 2005, 39: 925-936. 10.1016/j.freeradbiomed.2005.05.009

    Article  CAS  PubMed  Google Scholar 

  16. Haase VH: The VHL/HIF oxygen-sensing pathway and its relevance to kidney disease. Kidney Int 2006, 69: 1302-1307.

    CAS  PubMed  Google Scholar 

  17. Koivunen P, Hirsila M, Remes AM, Hassinen IE, Kivirikko KI, Myllyharju J: Inhibition of hypoxia-inducible factor (HIF) hydroxylases by citric acid cycle intermediates: possible links between cell metabolism and stabilization of HIF. J Biol Chem 2007, 282: 4524-4532. 10.1074/jbc.M610415200

    Article  CAS  PubMed  Google Scholar 

  18. Serra-Perez A, Planas AM, Nunez-O'Mara A, et al.: Extended ischemia prevents HIF1 alpha degradation at reoxygenation by impairing prolylhydroxylation: role of Krebs cycle metabolites. J Biol Chem 2010, 285: 18217-1824. 10.1074/jbc.M110.101048

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  19. Rosenberger C, Rosen S, Heyman SN: Renal Parenchymal Oxygenation and Hypoxia Adaptation in Acute Kidney Injury. Clin Exp Pharmacol Physiol 2006, 33: 980-988. 10.1111/j.1440-1681.2006.04472.x

    Article  CAS  PubMed  Google Scholar 

  20. Heyman SN, Khamaisi M, Rosen S, Rosenberger C: Renal parenchymal hypoxia, hypoxia response and the progression of chronic kidney disease. Am J Nephrol 2008, 28: 998-1006. 10.1159/000146075

    Article  CAS  PubMed  Google Scholar 

  21. Rosenberger C, Mandriota S, Jurgensen JS, et al.: Expression of hypoxiainducible factor-1alpha and -2alpha in hypoxic and ischemic rat kidneys. J Am Soc Nephrol 2002, 13: 1721-1732. 10.1097/01.ASN.0000017223.49823.2A

    Article  CAS  PubMed  Google Scholar 

  22. Rosenberger C, Shina A, Rosen S, Goldfarb M, Eckardt K, Heyman SN: Hypoxia inducible factors and tubular cell survival in isolated perfused kidneys. Kidney Int 2006, 70: 60-70. 10.1038/

    Article  CAS  PubMed  Google Scholar 

  23. Rosenberger C, Heyman SN, Rosen S, et al.: Upregulation of HIF in acute renal failure - evidence for a protective transcriptional response to hypoxia. Kidney Int 2005, 67: 531-542. 10.1111/j.1523-1755.2005.67110.x

    Article  CAS  PubMed  Google Scholar 

  24. Paliege A, Rosenberger C, Bondke A, et al.: Hypoxia-inducible factor-2α-expressing interstitial fibroblasts are the only renal cells that express erythropoietin under hypoxia-inducible factor stabilization. Kidney Int 2010, 77: 312-318. 10.1038/ki.2009.460

    Article  CAS  PubMed  Google Scholar 

  25. Rosenberger C, Griethe W, Gruber G, et al.: Cellular responses to hypoxia after renal segmental infarction. Kidney Int 2003, 64: 874-886. 10.1046/j.1523-1755.2003.00159.x

    Article  PubMed  Google Scholar 

  26. Rosenberger C, Goldfarb M, Shina A, et al.: Evidence for sustained renal hypoxia and transient hypoxia adaptation in experimental rhabdomyolysis-induced acute kidney injury. Nephrol Dial Transpl 2008, 23: 1135-1143. 10.1093/ndt/gfm808

    Article  CAS  Google Scholar 

  27. Cursio R, Miele C, Filippa N, Van Obberghen E, Gugenheim J: Liver HIF-1 alpha induction precedes apoptosis following normothermic ischemia-reperfusion in rats. Transplant Proc 2008, 40: 2042-2045. 10.1016/j.transproceed.2008.05.037

    Article  CAS  PubMed  Google Scholar 

  28. Heyman SN, Rosenberger C, Rosen S: Experimental ischemia-reperfusion - biases and myths: the proximal vs. distal hypoxic tubular injury debate revisited. Kidney Int 2010, 77: 9-16. 10.1038/ki.2009.347

    Article  PubMed  Google Scholar 

  29. Goldfarb M, Rosenberger C, Abassi Z, et al.: Acute-on-chronic renal failure in the rat: Functional compensation and hypoxia tolerance. Am J Nephrol 2006, 26: 22-33. 10.1159/000091783

    Article  PubMed  Google Scholar 

  30. Rosenberger C, Khamaisi M, Abassi Z, et al.: Adaptation to hypoxia in the diabetic rat kidney. Kidney Int 2008, 73: 34-42. 10.1038/

    Article  CAS  PubMed  Google Scholar 

  31. Rosenberger C, Pratschke J, Rudolph B, et al.: Immunohistochemical Detection of Hypoxia-Inducible Factor-1alpha in Human Renal Allograft Biopsies. J Am Soc Nephrol 2007, 18: 343-351. 10.1681/ASN.2006070792

    Article  CAS  PubMed  Google Scholar 

  32. Hill P, Shukla D, Tran MG, et al.: Inhibition of hypoxia inducible factor hydroxylases protects against renal ischemia-reperfusion injury. J Am Soc Nephrol 2008, 19: 39-46. 10.1681/ASN.2006090998

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  33. Jones NM, Lee EM, Brown TG, Jarrott B, Beart PM: Hypoxic preconditioning produces differential expression of hypoxia-inducible factor-1alpha (HIF-1alpha) and its regulatory enzyme HIF prolyl hydroxylase 2 in neonatal rat brain. Neurosci Lett 2006, 404: 72-77. 10.1016/j.neulet.2006.05.049

    Article  CAS  PubMed  Google Scholar 

  34. May D, Gilon D, Djonov V, et al.: Transgenic system for conditional induction and rescue of chronic myocardial hibernation provides insights into genomic programs of hibernation. Proc Natl Acad Sci USA 2008, 105: 282-287. 10.1073/pnas.0707778105

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  35. Pugh CW, Ratcliffe PJ: Regulation of angiogenesis by hypoxia: role of the HIF system. Nat Med 2003, 9: 677-684. 10.1038/nm0603-677

    Article  CAS  PubMed  Google Scholar 

  36. Yang CC, Lin LC, Wu MS, Chien CT, Lai MK: Repetitive hypoxic preconditioning attenuates renal ischemia/reperfusion induced oxidative injury via upregulating HIF-1 alpha-dependent bcl-2 signaling. Transplantation 2009, 88: 1251-1260. 10.1097/TP.0b013e3181bb4a07

    Article  CAS  PubMed  Google Scholar 

  37. Hsieh MM, Linde NS, Wynter A, et al.: HIF prolyl hydroxylase inhibition results in endogenous erythropoietin induction, erythrocytosis, and modest fetal hemoglobin expression in rhesus macaques. Blood 2007, 110: 2140-2147. 10.1182/blood-2007-02-073254

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  38. Rosenberger C, Rosen S, Shina A, et al.: Activation of hypoxia inducible factors (HIF) ameliorates hypoxic distal tubular injury in the isolated perfused rat kidney. Nephrol Dial transplant 2008, 23: 3472-3478. 10.1093/ndt/gfn276

    Article  CAS  PubMed  Google Scholar 

  39. Manotham K, Tanaka T, Ohse T, et al.: A biologic role of HIF-1 in the renal medulla. Kidney Int 2005, 67: 1428-1439. 10.1111/j.1523-1755.2005.00220.x

    Article  CAS  PubMed  Google Scholar 

  40. Bernhardt WM, Campean V, Kany S, et al.: Preconditional activation of hypoxia-inducible factors ameliorates ischemic acute renal failure. J Am Soc Nephrol 2006, 17: 1970-1978. 10.1681/ASN.2005121302

    Article  CAS  PubMed  Google Scholar 

  41. Bernhardt WM, Gottmann U, Doyon F, et al.: Donor treatment with a PHD inhibitor activating HIFs prevents graft injury and prolongs survival in an allogenic kidney transplant model. Proc Natl Acad Sci USA 2009, 106: 21276-21281. 10.1073/pnas.0903978106

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  42. Weidemann A, Bernhardt WM, Klanke B, et al.: HIF activation protects from acute kidney injury. J Am Soc Nephrol 2008, 19: 486-494. 10.1681/ASN.2007040419

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  43. Ockaili R, Natarajan R, Salloum F, et al.: HIF-1 activation attenuates postischemic myocardial injury: role for heme oxygenase-1 in modulating microvascular chemokine generation. Am J Physiol Heart Circ Physiol 2005, 289: H542-H548. 10.1152/ajpheart.00089.2005

    Article  CAS  PubMed  Google Scholar 

  44. Philipp S, Jurgensen JS, Fielitz J, et al.: Stabilization of hypoxia inducible factor rather than modulation of collagen metabolism improves cardiac function after acute myocardial infarction in rats. Eur J Heart Fail 2006, 8: 347-354. 10.1016/j.ejheart.2005.10.009

    Article  CAS  PubMed  Google Scholar 

  45. Kant R, Diwan V, Jaggi AS, Singh N, Singh D: Remote renal preconditioning-induced cardioprotection: a key role of hypoxia inducible factor-prolyl 4-hydroxylases. Mol Cell Biochem 2008, 312: 25-31. 10.1007/s11010-008-9717-5

    Article  CAS  PubMed  Google Scholar 

  46. Zolk O, Solbach TF, Eschenhagen T, Weidemann A, Fromm MF: Activation of negative regulators of the hypoxia-inducible factor (HIF) pathway in human end-stage heart failure. Biochem Biophys Res Commun 2008, 376: 315-320. 10.1016/j.bbrc.2008.08.152

    Article  CAS  PubMed  Google Scholar 

  47. Horowitz M, Assadi H: Heat acclimation-mediated cross-tolerance in cardioprotection: do HSP70 and HIF-1alpha play a role? Ann N Y Acad Sci 2010, 1188: 199-206. 10.1111/j.1749-6632.2009.05101.x

    Article  CAS  PubMed  Google Scholar 

  48. Wu Y, Li X, Xie W, Jankovic J, Le W, Pan T: Neuroprotection of deferoxamine on rotenone-induced injury via accumulation of HIF-1 alpha and induction of autophagy in SH-SY5Y cells. Neurochem Int 2010, 57: 98-205.

    CAS  Google Scholar 

  49. Harten SK, Ashcroft M, Maxwell PH: Prolyl hydroxylase domain inhibitors: a route to HIF activation and neuroprotection. Antioxid Redox Signal 2010, 12: 459-480. 10.1089/ars.2009.2870

    Article  CAS  PubMed  Google Scholar 

  50. Niatsetskaya Z, Basso M, Speer RE, et al.: HIF prolyl hydroxylase inhibitors prevent neuronal death induced by mitochondrial toxins: therapeutic implications for Huntington's disease and Alzheimer's disease. Antioxid Redox Signal 2010, 12: 435-443. 10.1089/ars.2009.2800

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  51. Siddiq A, Aminova LR, Troy CM, et al.: Selective inhibition of hypoxiainducible factor (HIF) prolyl-hydroxylase 1 mediates neuroprotection against normoxic oxidative death via HIF- and CREB-independent pathways. J Neurosci 2009, 29: 8828-8838. 10.1523/JNEUROSCI.1779-09.2009

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  52. Grover TR, Asikainen TM, Kinsella JP, Abman SH, White CW: Hypoxia-inducible factors HIF-1alpha and HIF-2alpha are decreased in an experimental model of severe respiratory distress syndrome in preterm lambs. Am J Physiol Lung Cell Mol Physiol 2007, 292: L1345-L1351. 10.1152/ajplung.00372.2006

    Article  CAS  PubMed  Google Scholar 

  53. Tajima T, Goda N, Fujiki N, et al.: HIF-1alpha is necessary to support gluconeogenesis during liver regeneration. Biochem Biophys Res Commun 2009, 387: 789-794. 10.1016/j.bbrc.2009.07.115

    Article  CAS  PubMed  Google Scholar 

  54. Milkiewicz M, Pugh CW, Egginton S: Inhibition of endogenous HIF inactivation induces angiogenesis in ischaemic skeletal muscles of mice. J Physiol 2004, 560: 21-26. 10.1113/jphysiol.2004.069757

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  55. Rey S, Lee K, Wang CJ, et al.: Synergistic effect of HIF-1alpha gene therapy and HIF-1-activated bone marrow-derived angiogenic cells in a mouse model of limb ischemia. Proc Natl Acad Sci USA 2009, 106: 20399-20404. 10.1073/pnas.0911921106

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  56. James LP, Donahower B, Burke AS, McCullough S, Hinson JA: Induction of the nuclear factor HIF-1alpha in acetaminophen toxicity: evidence for oxidative stress. Biochem Biophys Res Commun 2006, 343: 171-176. 10.1016/j.bbrc.2006.02.143

    Article  CAS  PubMed  Google Scholar 

  57. Kang MJ, Kim HJ, Kim HK, et al.: The effect of age and calorie restriction on HIF-1-responsive genes in aged liver. Biogerontology 2005, 6: 27-37. 10.1007/s10522-004-7381-z

    Article  CAS  PubMed  Google Scholar 

  58. Serchov T, Dubois-Pot-Schneider H, Charlot C, Rosl F, Wasylyk B: Involvement of net and HIF-1alpha in distinct yet intricately linked hypoxia-induced signaling pathways. J Biol Chem 2010, 285: 21223-21232. 10.1074/jbc.M110.121723

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  59. Nechemia-Arbely Y, Rosenberger C, Khamaisi M, Koesters R, Shina A, Klaus S, Shriki A, Rosen S, Axelrod JH, Heyman SN: Renal hypoxia inducible factors (HIF) and STAT3 cross-talk in vivo [abstract]. J Am Soc Nephrol 2009, 20: F-FC184.

    Google Scholar 

  60. Jokilehto T, Jaakkola PM: The role of HIF prolyl hydroxylases in tumour growth. J Cell Mol Med 2010, 14: 758-770. 10.1111/j.1582-4934.2010.01030.x

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  61. Higgins DF, Kimura K, Bernhardt WM, et al.: Hypoxia promotes fibrogenesis in vivo via HIF-1 stimulation of epithelial-to-mesenchymal transition. J Clin Invest 2007, 117: 3810-3820.

    PubMed Central  CAS  PubMed  Google Scholar 

  62. Nevo O, Soleymanlou N, Wu Y, et al.: Increased expression of sFlt-1 in in vivo and in vitro models of human placental hypoxia is mediated by HIF-1. Am J Physiol Regul Integr Comp Physiol 2006, 291: R1085-R1093. 10.1152/ajpregu.00794.2005

    Article  CAS  PubMed  Google Scholar 

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This report was supported by the Israel Science Foundation (Grant No. 1473/08) and the Harvard Medical Faculty Physicians at Beth Israel Deaconess Medical Center, Boston, MA.

This article is one of eleven reviews selected from the Annual Update in Intensive Care and Emergency Medicine 2011 (Springer Verlag) and co-published as a series in Critical Care. Other articles in the series can be found online at Further information about the Annual Update in Intensive Care and Emergency Medicine is available from

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Correspondence to Samuel N Heyman.

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Heyman, S.N., Rosen, S. & Rosenberger, C. Hypoxia-inducible factors and the prevention of acute organ injury. Crit Care 15, 209 (2011).

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  • Acute Kidney Injury
  • Hypoxic Stress
  • Renal Clear Cell Carcinoma
  • Acute Hypoxic Stress
  • Cellular Reactive Oxygen Species Concentration