Scutt A, Williamson E M
Tissue Engineering Group, Department of Engineering Materials, Kroto Research Institute Nanoscience and Technology Centre, University of Sheffield, Broad Lane, Sheffield S3 7HQ, UK.
Calcif Tissue Int. 2007 Jan;80(1):50-9. doi: 10.1007/s00223-006-0171-7. Epub 2007 Jan 4.
Recently, the cannabinoid receptors CB(1) and CB(2) were shown to modulate bone formation and resorption in vivo, although little is known of the mechanisms underlying this. The effects of cannabinoids on mesenchymal stem cell (MSC) recruitment in whole bone marrow were investigated using either the fibroblastic colony-forming unit (CFU-f) assay or high-density cultures of whole bone marrow. Levels of the CB(1) and CB(2) receptors were assessed by flow cytometry. Treatment of CFU-f cultures with the endocannabinoid 2-arachidonylglycerol (2-AG) dose-dependently increased fibroblastic and differentiated colony formation along with colony size. The nonspecific agonists CP 55,940 and WIN 55,212 both increased colony numbers, as did the CB(2) agonists BML190 and JWH015. The CB(1)-specific agonist ACEA had no effect, whereas the CB(2) antagonist AM630 blocked the effect of the natural cannabinoid tetrahydrocannabivarin, confirming mediation via the CB(2) receptor. Treatment of primary bone marrow cultures with 2-AG stimulated proliferation and collagen accumulation, whereas treatment of subcultures of MSC had no effect, suggesting that the target cell is not the MSC but an accessory cell present in bone marrow. Subcultures of MSCs were negative for CB(1) and CB(2) receptors as shown by flow cytometry, whereas whole bone marrow contained a small population of cells positive for both receptors. These data suggest that cannabinoids may stimulate the recruitment of MSCs from the bone marrow indirectly via an accessory cell and mediated via the CB(2) receptor. This recruitment may be one mechanism responsible for the increased bone formation seen after cannabinoid treatment in vivo.
最近,大麻素受体CB(1)和CB(2)已被证明可在体内调节骨形成和骨吸收,尽管其潜在机制尚不清楚。使用成纤维细胞集落形成单位(CFU-f)测定法或全骨髓高密度培养法,研究了大麻素对全骨髓中间充质干细胞(MSC)募集的影响。通过流式细胞术评估CB(1)和CB(2)受体的水平。用内源性大麻素2-花生四烯酸甘油酯(2-AG)处理CFU-f培养物,可剂量依赖性地增加成纤维细胞和分化集落的形成以及集落大小。非特异性激动剂CP 55,940和WIN 55,212均可增加集落数量,CB(2)激动剂BML190和JWH015也有同样效果。CB(1)特异性激动剂ACEA无作用,而CB(2)拮抗剂AM630可阻断天然大麻素四氢大麻酚酸的作用,证实其通过CB(2)受体介导。用2-AG处理原代骨髓培养物可刺激增殖和胶原蛋白积累,而处理MSC传代培养物则无作用,这表明靶细胞不是MSC,而是骨髓中存在的辅助细胞。流式细胞术显示,MSC传代培养物中CB(1)和CB(2)受体呈阴性,而全骨髓中含有一小部分两种受体均呈阳性的细胞。这些数据表明,大麻素可能通过辅助细胞间接刺激骨髓中MSC的募集,并通过CB(2)受体介导。这种募集可能是大麻素体内治疗后骨形成增加的一种机制。