Details

Autor(en) / Beteiligte

• Chen, Xiaoguang
• Katakowski, Mark
• Li, Yi
• Lu, Dunyue
• Wang, Lei
• Zhang, Lijie
• Chen, Jieli
• Xu, Yongxian
• Gautam, Subhash
• Mahmood, Asim
• Chopp, Michael

Titel

Human bone marrow stromal cell cultures conditioned by traumatic brain tissue extracts: Growth factor production

Ist Teil von

• Journal of neuroscience research, 2002-09, Vol.69 (5), p.687-691

Ort / Verlag

New York: Wiley Subscription Services, Inc., A Wiley Company

Erscheinungsjahr

2002

Quelle

Access via Wiley Online Library

Beschreibungen/Notizen

• Treatment of traumatic brain injury (TBI) with bone marrow stromal cells (MSCs) improves functional outcome in the rat. However, the specific mechanisms by which introduced MSCs provide benefit remain to be elucidated. Currently, the ability of therapeutically transplanted MSCs to replace injured parenchymal CNS tissue appears limited at best. Tissue replacement, however, is not the only possible compensatory avenue in cell transplantation therapy. Various growth factors have been shown to mediate the repair and replacement of damaged tissue, so trophic support provided by transplanted MSCs may play a role in the treatment of damaged tissue. We therefore investigated the temporal profile of various growth factors, brain‐derived neurotrophic factor (BDNF), nerve growth factor (NGF), vascular endothelial growth factor (VEGF), basic fibroblast growth factor (bFGF), and hepatocyte growth factor (HGF), within cultures of human MSCs (hMSCs) conditioned with cerebral tissue extract from TBI. hMSCs were cultured with TBI extracts of rat brain in vitro and quantitative sandwich enzyme‐linked immunosorbent assays (ELISAs) were performed. TBI‐conditioned hMSCs cultures demonstrated a time‐dependent increase of BDNF, NGF, VEGF, and HGF, indicating a responsive production of these growth factors by the hMSCs. The ELISA data suggest that transplanted hMSCs may provide therapeutic benefit via a responsive secretion of an array of growth factors that can foster neuroprotection and angiogenesis. © 2002 Wiley‐Liss, Inc.