PMID- 22340401 OWN - NLM STAT- MEDLINE DCOM- 20120614 LR - 20181201 IS - 2542-5641 (Electronic) IS - 0366-6999 (Linking) VI - 124 IP - 24 DP - 2011 Dec TI - Increased expression of granulocyte colony-stimulating factor mediates mesenchymal stem cells recruitment after vascular injury. PG - 4286-92 AB - BACKGROUND: Recent studies indicate that bone marrow-derived cells may significantly contribute to atherosclerosis, post-angioplasty restenosis and transplantation-associated vasculopathy. The responsible bone marrow (BM) cells and mechanisms regulating the mobilization of these cells are currently unclear. The purpose of this study was to investigate the expression of granulocyte colony-stimulating factor (G-CSF) on injured arteries and its effects on mesenchymal stem cells (MSCs) differentiation into vascular smooth muscle cells (VSMCs) in the process of vascular remodeling. METHODS: Balloon-mediated vascular injury was established in female rats (n = 100) which received radioprotective whole female BM cells by tail vein injection and male MSCs through a tibial BM injection after lethal irradiation. The injured and contralateral carotid arteries were harvested at 3, 7, 14 and 28 days after treatment. RESULTS: Morphometric analysis indicated that intima to media area-ratio (I/M ratio) significantly increased at 28 days, 0.899 +/- 0.057 (P < 0.01), compared with uninjured arteries. Combining fluorescence in situ hybridization (FISH) and immunohistochemical analysis showed that a significant number of the neointimal cells derived from MSCs, (45.2 +/- 8.5)% at 28 days (P = 0.01), compared with (23.5 +/- 6.3)% at 14 days. G-CSF was induced in carotid arteries subject to balloon angioplasty (fold mRNA change = 8.67 +/- 0.63 at three days, relative G-CSF protein = 0.657 +/- 0.011 at three days, P < 0.01, respectively, compared with uninjured arteries). G-CSF was chemotactic for MSCs but did not affect the differentiation of MSCs into smooth-muscle-like cells. CONCLUSION: Increased expression of G-CSF by injured arteries plays an essential role in contribution to recruitment and homing of MSCs to the site of the arterial lesion. FAU - Zhao, Yong AU - Zhao Y AD - Department of Cardiology, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, Guangdong 510120, China. FAU - Liu, Ying-Xi AU - Liu YX FAU - Xie, Shuang-Lun AU - Xie SL FAU - Deng, Bing-Qing AU - Deng BQ FAU - Wang, Jing-Feng AU - Wang JF FAU - Nie, Ru-Qiong AU - Nie RQ LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - China TA - Chin Med J (Engl) JT - Chinese medical journal JID - 7513795 RN - 143011-72-7 (Granulocyte Colony-Stimulating Factor) SB - IM MH - Angioplasty, Balloon MH - Animals MH - Blotting, Western MH - Carotid Arteries/surgery MH - Cell Differentiation MH - Cell Movement MH - Cells, Cultured MH - Enzyme-Linked Immunosorbent Assay MH - Female MH - Granulocyte Colony-Stimulating Factor/*metabolism MH - Immunohistochemistry MH - In Situ Hybridization, Fluorescence MH - Male MH - Mesenchymal Stem Cells/*cytology MH - Myocytes, Smooth Muscle/cytology MH - Neointima/surgery/therapy MH - Rats MH - Rats, Sprague-Dawley MH - Reverse Transcriptase Polymerase Chain Reaction MH - Vascular System Injuries/*surgery/*therapy EDAT- 2012/02/22 06:00 MHDA- 2012/06/15 06:00 CRDT- 2012/02/21 06:00 PHST- 2012/02/21 06:00 [entrez] PHST- 2012/02/22 06:00 [pubmed] PHST- 2012/06/15 06:00 [medline] PST - ppublish SO - Chin Med J (Engl). 2011 Dec;124(24):4286-92.