Dental and Craniofacial Research Institute, University of California, Los Angeles, Los Angeles, California 90095-1579, USA.
Tissue Eng Part A. 2011 Oct;17(19-20):2497-509. doi: 10.1089/ten.TEA.2010.0705. Epub 2011 Jul 18.
The search for novel sources of stem cells other than bone marrow mesenchymal stem cells (MSCs) for bone regeneration and repair has been a critical endeavor. We previously established an effective protocol to homogeneously purify human pericytes from multiple fetal and adult tissues, including adipose, bone marrow, skeletal muscle, and pancreas, and identified pericytes as a primitive origin of human MSCs. In the present study, we further characterized the osteogenic potential of purified human pericytes combined with a novel osteoinductive growth factor, Nell-1. Purified pericytes grown on either standard culture ware or human cancellous bone chip (hCBC) scaffolds exhibited robust osteogenic differentiation in vitro. Using a nude mouse muscle pouch model, pericytes formed significant new bone in vivo as compared to scaffold alone (hCBC). Moreover, Nell-1 significantly increased pericyte osteogenic differentiation, both in vitro and in vivo. Interestingly, Nell-1 significantly induced pericyte proliferation and was observed to have pro-angiogenic effects, both in vitro and in vivo. These studies suggest that pericytes are a potential new cell source for future efforts in skeletal regenerative medicine, and that Nell-1 is a candidate growth factor able to induce pericyte osteogenic differentiation.
除骨髓间充质干细胞(MSCs)以外,寻找新型的干细胞来源以促进骨骼再生和修复一直是一项关键的研究工作。我们先前建立了一种有效的方法,能够从包括脂肪、骨髓、骨骼肌和胰腺在内的多种胎儿和成体组织中均匀地纯化人周细胞,并确定周细胞是人类 MSCs 的原始来源。在本研究中,我们进一步研究了纯化的人周细胞与新型成骨诱导生长因子 Nell-1 联合应用的成骨潜能。在标准培养器皿或人松质骨芯片(hCBC)支架上培养的纯化周细胞在体外表现出强大的成骨分化能力。使用裸鼠肌肉囊模型,与支架(hCBC)单独相比,周细胞在体内形成了显著的新骨。此外,Nell-1 显著增加了周细胞的体外和体内成骨分化。有趣的是,Nell-1 显著诱导了周细胞的增殖,并在体外和体内观察到具有促血管生成作用。这些研究表明,周细胞是未来骨骼再生医学中一种潜在的新细胞来源,而 Nell-1 是一种能够诱导周细胞成骨分化的候选生长因子。