Lin Guiting, Garcia Maurice, Ning Hongxiu, Banie Lia, Guo Ying-Lu, Lue Tom F, Lin Ching-Shwun
Knuppe Molecular Urology Laboratory, Department of Urology, School of Medicine, University of California, San Francisco, California 94143-0738, USA.
Stem Cells Dev. 2008 Dec;17(6):1053-63. doi: 10.1089/scd.2008.0117.
Adipose tissue-derived stem cells (ADSC) are routinely isolated from the stromal vascular fraction (SVF) of homogenized adipose tissue. Freshly isolated ADSC display surface markers that differ from those of cultured ADSC, but both cell preparations are capable of multipotential differentiation. Recent studies have inferred that these progenitors may reside in a perivascular location where they appeared to coexpress CD34 and smooth muscle actin (alpha-SMA) but not CD31. However, these studies provided only limited histological evidence to support such assertions. In the present study, we employed immunohistochemistry and immunofluorescence to define more precisely the location of ADSC within human adipose tissue. Our results show that alpha-SMA and CD31 localized within smooth muscle and endothelial cells, respectively, in all blood vessels examined. CD34 localized to both the intima (endothelium) and adventitia neither of which expressed alpha-SMA. The niche marker Wnt5a was confined exclusively to the vascular wall within mural smooth muscle cells. Surprisingly, the widely accepted mesenchymal stem cell marker STRO-1 was expressed exclusively in the endothelium of capillaries and arterioles but not in the endothelium of arteries. The embryonic stem cell marker SSEA1 localized to a pericytic location in capillaries and in certain smooth muscle cells of arterioles. Cells expressing the embryonic stem cell markers telomerase and OCT4 were rare and observed only in capillaries. Based on these findings and evidence gathered from the existing literature, we propose that ADSC are vascular precursor (stem) cells at various stages of differentiation. In their native tissue, ADSC at early stages of differentiation can differentiate into tissue-specific cells such as adipocytes. Isolated, ADSC can be induced to differentiate into additional cell types such as osteoblasts and chondrocytes.
脂肪组织来源的干细胞(ADSC)通常从匀浆化脂肪组织的基质血管成分(SVF)中分离得到。新鲜分离的ADSC表现出与培养的ADSC不同的表面标志物,但两种细胞制剂都具有多能分化能力。最近的研究推断,这些祖细胞可能位于血管周围位置,在那里它们似乎共表达CD34和平滑肌肌动蛋白(α-SMA),但不表达CD31。然而,这些研究仅提供了有限的组织学证据来支持此类断言。在本研究中,我们采用免疫组织化学和免疫荧光更精确地确定ADSC在人脂肪组织中的位置。我们的结果表明,在所有检查的血管中,α-SMA和CD31分别定位于平滑肌细胞和内皮细胞。CD34定位于内膜(内皮)和外膜,两者均不表达α-SMA。小生境标志物Wnt5a仅局限于壁平滑肌细胞内的血管壁。令人惊讶的是,广泛接受的间充质干细胞标志物STRO-1仅在毛细血管和小动脉的内皮中表达,而不在动脉内皮中表达。胚胎干细胞标志物SSEA1定位于毛细血管和小动脉某些平滑肌细胞的周细胞位置。表达胚胎干细胞标志物端粒酶和OCT4的细胞很少见,仅在毛细血管中观察到。基于这些发现以及从现有文献中收集的证据,我们提出ADSC是处于不同分化阶段的血管前体(干)细胞。在其天然组织中,处于分化早期的ADSC可以分化为组织特异性细胞,如脂肪细胞。分离后,ADSC可以被诱导分化为其他细胞类型,如成骨细胞和软骨细胞。