- Open Access
Plasma gelsolin levels and outcomes after aneurysmal subarachnoid hemorrhage
Critical Care volume 17, Article number: R149 (2013)
Lower gelsolin levels have been associated with the severity and poor outcome of critical illness. Nevertheless, their link with clinical outcomes of aneurysmal subarachnoid hemorrhage is unknown. Therefore, we aimed to investigate the relationship between plasma gelsolin levels and clinical outcomes in patients with aneurysmal subarachnoid hemorrhage.
A total of 262 consecutive patients and 150 healthy subjects were included. Plasma gelsolin levels were measured by enzyme-linked immunosorbent assay. Mortality and poor long-term outcome (Glasgow Outcome Scale score of 1-3) at 6 months were recorded.
Plasma gelsolin levels on admission were substantially lower in patients than in healthy controls (66.9 (26.4) mg/L vs. 126.4 (35.4) mg/L, P < 0.001), and negatively associated with World Federation of Neurological Surgeons score (r = -0.554, P < 0.001) and Fisher score (r = -0.538, P < 0.001), and identified as an independent predictor of poor functional outcome (odds ratio, 0.957; 95% confidence interval (CI), 0.933-0.983; P = 0.001) and death (odds ratio, 0.953; 95% CI, 0.917-0.990; P = 0.003) after 6 months. The areas under the ROC curve of gelsolin for functional outcome and mortality were similar to those of World Federation of Neurological Surgeons score and Fisher score (all P > 0.05). Gelsolin improved the predictive values of World Federation of Neurological Surgeons score and Fisher score for functional outcome (both P < 0.05), but not for mortality (both P > 0.05).
Gelsolin levels are a useful, complementary tool to predict functional outcome and mortality 6 months after aneurysmal subarachnoid hemorrhage.
Plasma gelsolin is the extracellular isoform of a ubiquitous cytoplasmic actin-binding protein, gelsolin, which mediates cell shape changes and motility . Plasma gelsolin is associated with the severity and outcome of critical illness, and therefore, has been proposed as a prognostic marker in acute illness [2–11]. Recently, it has been reported that plasma gelsolin levels were also decreased in the patients with traumatic brain injury , ischemic stroke , and intracerebral hemorrhage ; in these groups of patients, low gelsolin levels were highly predictive for mortality. Gelsolin has been also found to be depleted in the peripheral blood of patients with aneurysmal subarachnoid hemorrhage (SAH) . However, no published information exists to date about the correlation of gelsolin with outcome after aneurysmal SAH. The present study aimed to investigate this correlation and to analyze the usefulness of gelsolin as a predictor of long-term functional outcome and mortality in aneurysmal SAH.
Materials and methods
Between June 2008 and August 2011, all patients with aneurysmal SAH confirmed by computed tomography (CT) angiography with or without digital subtraction angiography who were admitted to Department of Neurosurgery, The First Affiliated Hospital, School of Medicine, Zhejiang University were evaluated in the study. Inclusion criteria were clinical history of SAH within the last 24 h before admission and the treatment by surgery or coiling within 48 h after admission. Exclusion criteria were rebleeding after admission, aged <18 years, existing previous head trauma, neurological disease, use of antiplatelet or anticoagulant medication, presence of other prior systemic diseases including uremia, liver cirrhosis, malignancy, chronic heart or lung disease, diabetes mellitus, and hypertension. Healthy individuals were evaluated as controls if they presented to our hospital and had blood collected as part of medical examination in May 2011. The study was conducted in accordance with the guidelines approved by the Human Research Ethics Committee at The First Affiliated Hospital, School of Medicine, Zhejiang University. Written informed consent was obtained from the study subjects or their relatives.
Clinical and radiological assessment
At admission, clinical severity was assessed using the World Federation of Neurological Surgeons (WFNS) score as follows: 1 = Glasgow Coma Scale (GCS) score of 15, no motor deficit; 2 = GCS score of 13-14, no motor deficit; 3 = GCS score of 13-14 and any motor deficit or aphasia; 4 = GCS score of 7-12, with or without motor deficit; and 5 = GCS of 3 to 6, with or without motor deficit . The initial CT was classified according to the modified Fisher score as follows: grade 1 = no subarachnoid blood; grade 2 = broad diffusion of subarachnoid blood; grade 3 = with clots or thick layers of subarachnoid blood; grade 4 = intraventricular hemorrhage or intracerebral hematoma, no clot; and grade 5 = intraventricular hemorrhage or intracerebral hematoma with clot . All CT scans were performed according to the neuroradiology department protocol. Investigators who read them were blinded to clinical information.
The type of treatment (surgery or coiling) was decided according to both location and size of the aneurysm by the neurosurgeon and the neuroradiologist. All patients received intravenous Nimodipine at a dose of 2 mg/h from admission until at least day 14, except during periods of uncontrolled increased intracranial pressure during which intravenous Nimodipine was discontinued. Seizures were systematically prevented by Sodium Valproate (200 mg × 3, per os). After surgery or coiling, patients were managed with 'triple H' therapy (hypertension with a mean arterial pressure goal >100 mm Hg, hypervolemia, and hemodilution with a goal hematocrit of 30) through 12 days after hemorrhage. An external ventricular drain was inserted in case of hydrocephalus on CT and in patients with a high WFNS grade (WFNS score of 3 to 5). Increased intracranial pressure was treated by cerebrospinal fluid drainage, mechanical ventilation, reinforcement of sedation, and, rarely, moderate hypothermia. CT was performed whenever clinical deterioration occurred to search for secondary complications such as hydrocephalus or ischemia.
Clinical onset of cerebral vasospasm was defined as the acute onset of a focal neurologic deficit or a change in the GCS score of 2 or more points. All suspected cases of cerebral vasospasms were confirmed by CT angiography and were then taken to the interventional radiology suite for cerebral angiography. Each vasospasm episode was treated with intra-arterial administration of Nimodipine as recently described. This therapy was repeated if necessary. Balloon angioplasty was used as a second-line therapy when Nimodipine was judged insufficient.
Determination of gelsolin in plasma
The informed consents were obtained from study population or family members in all cases before the blood were collected. Venous blood in the healthy individuals or the patients was drawn at study entry or on admission. The blood samples were immediately placed into sterile EDTA test tubes and centrifuged at 1,500 g for 20 min at 4°C to collect plasma. Plasma was stored at -70°C until assayed. The concentration of gelsolin in plasma was analyzed by enzyme-linked immunosorbent assay (ELISA) using commercial kits (CoTimes, Beijing, China) in accordance with the manufactures' instructions. Intra-assay and inter-assay coefficients of variation were 4.2% and 6.8%, respectively. The blood samples were run in duplicate. Researchers running ELISAs were blinded to all patient details.
Participants were followed up until death or completion of 6 months after SAH. The endpoints were unfavorable outcome and death after 6 months. The functional outcome was defined by Glasgow outcome scale (GOS) score. GOS was defined as follows: 1 = death; 2 = persistent vegetative state; 3 = severe disability; 4 = moderate disability; and 5 = good recovery . GOS scores were dichotomized in favorable and unfavorable outcomes (GOS of 4-5 vs. GOS of 1-3). For follow-up, structured telephone interviews were performed by one doctor who was blinded to clinical information and gelsolin levels.
Statistical analysis was performed with SPSS 10.0 (SPSS Inc., Chicago, IL, USA) and MedCalc 126.96.36.199. (MedCalc Software, Mariakerke, Belgium). The normality of data distribution was assessed by the Kolmogorovor-Smirnov test or Shapiro-Wilk test. All values are expressed as median (interquartile range), mean ± standard deviation or counts (percentage) unless otherwise specified. Comparisons were made by using: (1) chi-square test or Fisher exact test for categorical data; (2) unpaired Student t test for continuous normally distributed variables; and (3) the Mann-Whitney U-test for continuous non-normally distributed variables. Correlations of gelsolin with other variables were assessed by Spearman's correlation coefficient. The relations of gelsolin to the poor functional outcome (GOS 1-3) and death were assessed in a logistic-regression model. For multivariate analysis, we included the significantly different outcome predictors as assessed in univariate analysis. A ROC curve was configured to establish the cutoff point of plasma gelsolin with the optimal sensitivity and specificity for predicting the poor functional outcome (GOS 1-3) and mortality. A P value < 0.05 was considered statistically significant.
Study population characteristics
During the recruitment period, 308 patients were admitted with an initial diagnosis of aneurysmal SAH, 269 (87.3%) patients fulfilled the inclusion criteria and exclusion criteria, and adequate data on admission and follow-up were available for 262 individuals (112 men and 150 women) (85.1%) who were finally included in the analysis. Table 1 summarized the other demographic, clinical, laboratory and radiological data from baseline CT scans of the patients. A control group consisted of 150 healthy individuals. The intergroup differences of patients and healthy controls in the age and sex were not statistically significant (both P > 0.05).
The change of plasma gelsolin level in SAH patients
Plasma gelsolin values are continuous non-normally distributed variables. Therefore, all values are expressed as median (interquartile range). Using the Mann-Whitney U-test, the admission gelsolin levels were significantly decreased in all patients (66.9 (26.4) mg/L), survivals (70.3 (25.5) mg/L), non-survivals (49.0 (17.9) mg/L), patients with favorable outcome (75.7 (22.6) mg/L), and those with unfavorable outcome (52.8 (17.5) mg/L) compared with healthy control individuals (126.4 (35.4) mg/L, all P < 0.001) (Figure 1).
Correlations of plasma gelsolin level with disease severity
In all 262 patients with aneurysmal SAH, a significant correlation emerged between WFNS scores and plasma gelsolin level (r=-0.554, P < 0.001), as well as between Fisher scores and plasma gelsolin level (r=-0.538, P < 0.001) using Spearman's correlation coefficient (Figure 2).
Poor neurologic function prediction
Seventy-three patients (27.9%) suffered from poor neurologic outcome (GOS 1-3) in 6 months. Table 2 shows that there was a significantly higher likelihood of poor neurologic outcome at 6 months in patients that have higher WFNS score, Fisher score, glucose, C-reactive protein, fibrinogen and D-dimer concentration, and lower gelsolin level, and that more frequently showed intraventricular hemorrhage, external ventricular drain, vasospasm, and CT ischemia. When the above variables found to be significant in the univariate analysis were introduced into the logistic model, a multivariate analyses selected WFNS score (odds ratio, 7.947; 95% confidence interval (CI), 1.398-16.210; P = 0.004), Fisher score (odds ratio, 9.772; 95% CI, 2.278-21.012; P = 0.002), and plasma gelsolin level (odds ratio, 0.957; 95% CI, 0.933-0.983; P = 0.001) as the independent predictors for 6-month poor neurologic outcome of patients.
A ROC curve identified that a baseline plasma gelsolin level < 63.3 mg/L predicted 6-month poor neurologic outcome of patients with 80.8% sensitivity and 75.1% specificity (area under curve (AUC), 0.841; 95% CI, 0.791-0.883) (Figure 3). The predictive value of the gelsolin concentration was thus similar to those of WFNS score (AUC, 0.894; 95% CI, 0.850-0.929) (P = 0.091) and Fisher score (AUC, 0.886; 95% CI, 0.841-0.922) (P = 0.170). In a combined logistic-regression model, gelsolin improved the AUC of WFNS score to 0.930 (95% CI, 0.892 - 0.957) (P = 0.016) and the AUC of Fisher score to 0.923 (95% CI, 0.884 - 0.952) (P = 0.032).
Thirty-one patients (11.8%) died from SAH in 6 months. Table 3 shows that there was a significantly higher likelihood of death at 6 months in patients that have higher WFNS score, Fisher score, glucose, C-reactive protein, fibrinogen and D-dimer concentration, and lower gelsolin level, and that more frequently showed intraventricular hemorrhage, external ventricular drain, vasospasm and CT ischemia. When the above variables found to be significant in the univariate analysis were introduced into the logistic model, a multivariate analyses selected WFNS score (odds ratio, 8.582; 95% CI, 2.028-18.484; P = 0.004), Fisher score (odds ratio, 9.594; 95% CI, 2.842-22.384; P = 0.003), and plasma gelsolin level (odds ratio, 0.953; 95% CI, 0.917-0.990; P = 0.003) as the independent predictors for 6-month mortality of patients.
A ROC curve identified that a baseline plasma gelsolin level < 52.5 mg/L predicted 6-month mortality of patients with 71.0% sensitivity and 89.2% specificity (AUC, 0.851; 95% CI, 0.802-0.892) (Figure 4). The predictive value of the gelsolin concentration was thus similar to those of WFNS score (AUC, 0.910; 95% CI, 0.869-0.942) (P = 0.146) and Fisher score (AUC, 0.927; 95% CI, 0.889-0.956) (P = 0.053). In a combined logistic-regression model, gelsolin improved the AUC of WFNS score to 0.938 (95% CI, 0.902-0.964), and improved the AUC of Fisher score to 0.950 (95% CI, 0.916-0.973), but the differences were not significant (P = 0.141 and 0.227).
In this post hoc analysis of prospective collected data, we demonstrated that plasma gelsolin levels on admission in the patients were significantly lower than those in healthy controls; and in patients who had poor functional outcome or died in 6 months, the gelsolin levels on admission were significantly lower compared with levels in survivors or those with good functional outcome. In multivariate logistic regression models of predictors of death and poor functional outcome, the gelsolin levels on admission were an independent predictor.
Gelsolin is an 80-kDa actin-binding protein and is the first and most widely expressed member of a family of actin-severing proteins, which includes adseverin and villin . After activation by micromolar Ca2+, gelsolin severs actin filaments, reducing actin cytoskeleton integrity, and remains bound to the barbed ends, inhibiting actin filament extension . Upon reduction in free Ca2+ to less than micromolar levels, and in the presence of polyphosphoinositides, gelsolin is released from the barbed ends, providing sites for rapid actin filament extension . Thus, gelsolin appears to serve a critical role in actin filament dynamics [21–24]. Based on its actin-binding property, plasma gelsolin has been categorized as part of the extracellular 'actin-scavenging' system that counteracts actin toxicity when actin is released into the extracellular space . Accordingly, the degree of plasma gelsolin depletion should reflect the degree of tissue injury that may lead to significant exposure of actin to the extracellular spaces. In every acute tissue injury setting examined, including toxic, hyperoxic, and idiopathic lung injury, adult respiratory distress syndrome, acute liver injury, myonecrosis, pancreatitis, trauma, burns and bacterial and protozoal sepsis, plasma gelsolin levels are subnormal [2–11]. The lower the levels of plasma gelsolin, the less favorable the prognosis of acute illness becomes [8–11]. Overall, gelsolin is associated with the severity and outcome of critical illness, and therefore, has been proposed as a prognostic marker in acute illness. Previous studies have shown significant predictive values of gelsolin in other acute brain injury including intracerebral hemorrhage, ischemic stroke, and traumatic brain injury [12–14]. This study showed that gelsolin was closely related to WFNS and Fisher scores, which in turn were associated with outcome of SAH in a multivariate regression model. Furthermore, gelsolin was identified as a reliable and independent marker to predict 6-month outcome in patients with SAH. Importantly, gelsolin's discriminative power (reflected by AUC) was in the range of WFNS and Fisher scores which are known to be a strong individual outcome predictor. Gelsolin improved AUC of WFNS and Fisher scores for functional outcome. However, gelsolin could not improve AUC of WFNS and Fisher scores for mortality. Overall, our data suggest that plasma gelsolin level in this early period might reflect the initial insult (as demonstrated by the close relation between gelsolin and WFNS score or Fisher scores) and gelsolin might have an interesting potential as a new prognostic biomarker.
The mechanism of plasma gelsolin's actions is poorly understood. Gelsolin was first discovered as an intracellular protein involved in actin dynamics . Plasma gelsolin was subsequently identified as a secreted isoform of the cytoplasmic gelsolin . Similar to cytoplasmic gelsolin, plasma gelsolin also severs and scavenges actin [28–30], a major body protein that may be exposed or released by cellular injury and that may enhance some major components of proinflammatory cytokine production, and impair the microcirculation and compromise multiple organs [31, 32]. In addition to actin, plasma gelsolin binds and modulates bioactive lipids, such as endotoxin , lysophosphatidic acid , and platelet activating factor . This effect may partially explain how exogenous gelsolin replacement significantly enhances survival of septic animals , and blunts the inflammatory response in animal models of lung injury  and burns . Based on these data, we propose that plasma gelsolin functions as an important endogenous guard against overwhelming inflammation from tissue injuries.
Gelsolin is constitutively expressed throughout the central nervous system and is particularly concentrated in neuronal growth cones . It has been demonstrated that gelsolin modulates voltage-dependent Ca2+ channels and N-methyl-D-aspartate receptor-coupled channel activity and reduces vulnerability to excitotoxicity in cultured hippocampal neurons after its activation by Ca2+  and that gelsolin -/- mice are more susceptible to brain injury after ischemia/reperfusion and gelsolin could serve as a neuroprotective factor in murine cerebral ischemia . Recent results suggested that enhanced gelsolin expression is an important mechanism by which histone deacetylase inhibitor trichostatin A protects against ischemic brain injury . A recent paper reported plasma gelsolin is decreased and correlated with rate of decline in Alzheimer's disease . From the available information, it is suggested that reversing plasma gelsolin deficiency may be an effective treatment for SAH.
In addition, univariate analysis showed that some parameters including blood glucose level, plasma C-reactive protein level, plasma fibrinogen level, and plasma D-dimer level were associated with 6-month poor functional outcome and mortality. But, a multivariate logistic regression did not verify these results. These differences may be caused by sample size or study design. However, this can supply some information about potentials of these biomarkers such as blood glucose level, plasma C-reactive protein level, plasma fibrinogen level, and plasma D-dimer level as outcome predictors in aneurysmal SAH.
In this study, gelsolin levels are associated with clinical severity and are a useful, complementary tool to predict functional outcome and mortality 6 months after aneurysmal subarachnoid hemorrhage.
In the patients with aneurysmal subarachnoid hemorrhage, plasma gelsolin level on admission was substantially lower than that in healthy controls.
Plasma gelsolin level was highly negatively associated with World Federation of Neurological Surgeons score and Fisher score after aneurysmal subarachnoid hemorrhage.
Plasma gelsolin level was an independent predictor of poor long-term functional outcome and death 6 months after aneurysmal subarachnoid hemorrhage.
Plasma gelsolin level was a useful, complementary tool to predict poor long-term functional outcome and mortality 6 months after aneurysmal subarachnoid hemorrhage.
enzyme-linked immunosorbent assay
Glasgow Coma Scale
Glasgow outcome scale
World Federation of Neurological Surgeons.
Silacci P, Mazzolai L, Gauci C, Stergiopulos N, Yin HL, Hayoz D: Gelsolin superfamily proteins: key regulators of cellular functions. Cell Mol Life Sci 2004, 61: 2614-2623. 10.1007/s00018-004-4225-6
Ito H, Kambe H, Kimura Y, Nakamura H, Hayashi E, Kishimoto T, Kishimoto S, Yamamoto H: Depression of plasma gelsolin level during acute liver injury. Gastroenterology 1992, 102: 1686-1692.
Suhler E, Lin W, Yin HL, Lee WM: Decreased plasma gelsolin concentrations in acute liver failure, myocardial infarction, septic shock, and myonecrosis. Crit Care Med 1997, 25: 594-598. 10.1097/00003246-199704000-00007
Huang S, Rhoads SL, DiNubile MJ: Temporal association between serum gelsolin levels and clinical events in a patient with severe falciparum malaria. Clin Infect Dis 1997, 24: 951-954. 10.1093/clinids/24.5.951
Dahl B, Schiødt FV, Ott P, Gvozdenovic R, Yin HL, Lee WM: Plasma gelsolin is reduced in trauma patients. Shock 1999, 12: 102-104. 10.1097/00024382-199908000-00002
Christofidou-Solomidou M, Scherpereel A, Solomides CC, Muzykantov VR, Machtay M, Albelda SM, DiNubile MJ: Changes in plasma gelsolin concentration during acute oxidant lung injury in mice. Lung 2002, 180: 91-104. 10.1007/s004080000084
Rothenbach PA, Dahl B, Schwartz JJ, O'Keefe GE, Yamamoto M, Lee WM, Horton JW, Yin HL, Turnage RH: Recombinant plasma gelsolin infusion attenuates burn-induced pulmonary microvascular dysfunction. J Appl Physiol 2004, 96: 25-31. 10.1063/1.1711178
Lee PS, Waxman AB, Cotich KL, Chung SW, Perrella MA, Stossel TP: Plasma gelsolin is a marker and therapeutic agent in animal sepsis. Crit Care Med 2007, 35: 849-855. 10.1097/01.CCM.0000253815.26311.24
Mounzer KC, Moncure M, Smith YR, Dinubile MJ: Relationship of admission plasma gelsolin levels to clinical outcomes in patients after major trauma. Am J Respir Crit Care Med 1999, 160: 1673-1681. 10.1164/ajrccm.160.5.9807137
Lee PS, Drager LR, Stossel TP, Moore FD, Rogers SO: Relationship of Plasma gelsolin levels to outcomes in critically ill surgical patients. Ann Surg 2006, 243: 399-403. 10.1097/01.sla.0000201798.77133.55
DiNubile MJ, Stossel TP, Ljunghusen OC, Ferrara JL, Antin JH: Prognostic implications of declining plasma gelsolin levels after allogeneic stem cell transplantation. Blood 2002, 100: 4367-4371. 10.1182/blood-2002-06-1672
Xu JF, Liu WG, Dong XQ, Yang SB, Fan J: Change in plasma gelsolin level after traumatic brain injury. J Trauma Acute Care Surg 2012, 72: 491-496.
Guo XC, Luo BY, Li XF, Yang DG, Zheng XN, Zhang K: Plasma gelsolin levels and 1-year mortality after first-ever ischemic stroke. J Crit Care 2011, 26: 608-612. 10.1016/j.jcrc.2011.02.007
Zhao DQ, Wang K, Zhang HD, Li YJ: Significant reduction of plasma gelsolin levels in patients with intracerebral hemorrhage. Clin Chim Acta 2013, 415: 202-206.
Chou SH, Lee PS, Konigsberg RG, Gallacci D, Chiou T, Arai K, Simmons S, Bauer D, Feske SK, Lo EH, Ning M: Plasma-type gelsolin is decreased in human blood and cerebrospinal fluid after subarachnoid hemorrhage. Stroke 2011, 42: 3624-3627. 10.1161/STROKEAHA.111.631135
Drake C: Report of World Federation of Neurological Surgeons Committee on a universal subarachnoid hemorrhage grading scale. J Neurosurg 1988, 68: 985-986.
Fisher CM, Kistler JP, Davis JM: Relation of cerebral vasospasm to subarachnoid hemorrhage visualized by computerized tomographic scanning. Neurosurgery 1980, 6: 1-9. 10.1227/00006123-198001000-00001
Jennett B, Bond M: Assessment of outcome after severe brain damage. Lancet 1975, 1: 480-484.
Schafer DA, Cooper JA: Control of actin assembly at filament ends. Annu Rev Cell Dev Biol 1995, 11: 497-518. 10.1146/annurev.cb.11.110195.002433
Janmey PA, Stossel TP: Modulation of gelsolin function by phosphatidylinositol 4,5-bisphosphate. Nature 1987, 325: 362-364. 10.1038/325362a0
Kwiatkowski DJ, Mehl R, Yin HL: Genomic organization and biosynthesis of secreted and cytoplasmic forms of gelsolin. J Cell Biol 1988, 106: 375-384. 10.1083/jcb.106.2.375
Kwiatkowski DJ, Janmey PA, Yin HL: Identification of critical functional and regulatory domains in gelsolin. J Cell Biol 1989, 108: 1717-1726. 10.1083/jcb.108.5.1717
Azuma T, Witke W, Stossel TP, Hartwig JH, Kwiatkowski DJ: Gelsolin is a downstream effector of rac for fibroblast motility. EMBO J 1998, 17: 1362-1370. 10.1093/emboj/17.5.1362
Witke W, Sharpe AH, Hartwig JH, Azuma T, Stossel TP, Kwiatkowski DJ: Hemostatic, inflammatory, and fibroblast responses are blunted in mice lacking gelsolin. Cell 1995, 81: 41-51. 10.1016/0092-8674(95)90369-0
Lee WM, Galbraith RM: The extracellular actin-scavenger system and actin toxicity. N Engl J Med 1992, 326: 1335-1341. 10.1056/NEJM199205143262006
Yin HL, Stossel TP: Control of cytoplasmic actin gel-sol transformation by gelsolin, a calcium-dependent regulatory protein. Nature 1979, 281: 583-586. 10.1038/281583a0
Kwiatkowski DJ, Stossel TP, Orkin SH, Mole JE, Colten HR, Yin HL: Plasma and cytoplasmic gelsolins are encoded by a single gene and contain a duplicated actin-binding domain. Nature 1986, 323: 455-458. 10.1038/323455a0
Janmey PA, Lind SE: Capacity of human serum to depolymerize actin filaments. Blood 1987, 70: 524-530.
Kwiatkowski DJ, Mehl R, Izumo S, Nadal-Ginard B, Yin HL: Muscle is the major source of plasma gelsolin. J Biol Chem 1988, 263: 8239-8243.
Lind SE, Smith DB, Janmey PA, Stossel TP: Role of plasma gelsolin and the vitamin D-binding protein in clearing actin from the circulation. J Clin Invest 1986, 78: 736-472. 10.1172/JCI112634
Haddad JG, Harper KD, Guoth M, Pietra GG, Sanger JW: Angiopathic consequences of saturating the plasma scavenger system for actin. Proc Natl Acad Sci USA 1990, 87: 1381-1385. 10.1073/pnas.87.4.1381
Rosengart MR, Arbabi S, Bauer GJ, Garcia I, Jelacic S, Maier RV: The actin cytoskeleton: an essential component for enhanced TNFalpha production by adherent monocytes. Shock 2002, 17: 109-113. 10.1097/00024382-200202000-00005
Bucki R, Georges PC, Espinassous Q, Funaki M, Pastore JJ, Chaby R, Janmey PA: Inactivation of endotoxin by human plasma gelsolin. Biochemistry 2005, 44: 9590-9597. 10.1021/bi0503504
Goetzl EJ, Lee H, Azuma T, Stossel TP, Turck CW, Karliner JS: Gelsolin binding and cellular presentation of lysophosphatidic acid. J Biol Chem 2000, 275: 14573-14578. 10.1074/jbc.275.19.14573
Osborn TM, Dahlgren C, Hartwig JH, Stossel TP: Modifications of cellular responses to lysophosphatidic acid and platelet-activating factor by plasma gelsolin. Am J Physiol Cell Physiol 2007, 292: C1323-1330.
Christofidou-Solomidou M, Scherpereel A, Solomides CC, Christie JD, Stossel TP, Goelz S, DiNubile MJ: Recombinant plasma gelsolin diminishes the acute inflammatory response to hyperoxia in mice. J Investig Med 2002, 50: 54-60. 10.2310/6650.2002.33518
Tanaka J, Kira M, Sobue K: Gelsolin is localized in neuronal growth cones. Brain Res Dev Brain Res 1993, 76: 268-271. 10.1016/0165-3806(93)90217-X
Furukawa K, Fu W, Li Y, Witke W, Kwiatkowski DJ, Mattson MP: The actin-severing protein gelsolin modulates calcium channel and NMDA receptor activities and vulnerability to excitotoxicity in hippocampal neurons. J Neurosci 1997, 17: 8178-8186.
Endres M, Fink K, Zhu J, Stagliano NE, Bondada V, Geddes JW, Azuma T, Mattson MP, Kwiatkowski DJ, Moskowitz MA: Neuroprotective effects of gelsolin during murine stroke. J Clin Invest 1999, 103: 347-351. 10.1172/JCI4953
Yildirim F, Gertz K, Kronenberg G, Harms C, Fink KB, Meisel A, Endres M: Inhibition of histone deacetylation protects wildtype but not gelsolin-deficient mice from ischemic brain injury. Exp Neurol 2008, 210: 531-542. 10.1016/j.expneurol.2007.11.031
Güntert A, Campbell J, Saleem M, O'Brien DP, Thompson AJ, Byers HL, Ward MA, Lovestone S: Plasma gelsolin is decreased and correlates with rate of decline in Alzheimer's disease. J Alzheimers Dis 2010, 21: 585-596.
The authors thank all staff in Department of Neurosurgery, The First Affiliated Hospital, School of Medicine, Zhejiang University for their technical support. This work was financially supported by the National Natural Science Foundation of China (No. 81200954) and Zhejiang Provincial Natural Science Foundation (No. LY12F02035).
The authors declare that they have no competing interests.
JWP and LNH contributed to the design of the study and drafted the manuscript and participated in the laboratory work. FX and JS enrolled the patients and contributed to data analysis and interpretation of the results. RYZ contributed to data analysis and interpretation of the results. All authors read and approved the final manuscript.
About this article
Cite this article
Pan, JW., He, LN., Xiao, F. et al. Plasma gelsolin levels and outcomes after aneurysmal subarachnoid hemorrhage. Crit Care 17, R149 (2013). https://doi.org/10.1186/cc12828
- Aneurysmal subarachnoid hemorrhage
- Functional outcome