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Abstract
Objective: Traumatic brain injury (TBI) promotes the recruitment of endothelial progenitor cells (EPCs) into the injured tissue where EPCs play an important role in repairing injured vasculature. However, the repair mechanism and prognostic significance of EPCs after TBI remain poorly understood.
Methods: Blood samples were collected from 21 patients with severe TBI and 20 healthy subjects. EPCs were quantified by flow cytometry and serum VEGF and MMP‐9 level measured by ELISA on days 1, 4, 7, 14 and 21 after TBI.
Results: EPCs in the patients decreased originally, then increased to the peak level at 7 days and was significantly correlated with GOS scores 6 months after TBI. VEGF and MMP‐9 were significantly increased during the follow‐up period after TBI. EPCs was also positively correlated with GCS score 1 day after TBI and with MMP‐9 and VEGF 7 days and 14 days after TBI.
Conclusion: The data demonstrate that TBI led to an increase of EPCs, VEGF and MMP‐9, suggesting that increased VEGF and MMP‐9 may mediate the recruitment of bone marrow‐derived EPCs into the circulation. The association of EPCs with nerve functional recovery in patients provides evidence that EPCs may be a potential biomarker to monitor TBI angiogenesis and prognosis.
Declaration of Interest: The work is supported by grants from the National Natural Science Foundation of China 30772229, 973 Project 2005CB522600 and NIH grant HL71895.The authors report no conflicts of interest. The authors alone are responsible for the content and writing of the paper.