Estes Bradley T, Diekman Brian O, Guilak Farshid
Department of Surgery, Duke University Medical Center, Durham, North Carolina 27710, USA.
Biotechnol Bioeng. 2008 Mar 1;99(4):986-95. doi: 10.1002/bit.21662.
Adipose-derived stem cells (ASCs) are an abundant, readily available population of multipotent progenitor cells that reside in adipose tissue. Isolated ASCs are typically expanded in monolayer on standard tissue culture plastic with a basal medium containing 10% fetal bovine serum. However, recent data suggest that altering the monolayer expansion conditions by using suspension culture plastic, adding growth factors to the medium, or adjusting the seeding density may affect the self-renewal rate, multipotency, and lineage-specific differentiation potential of the ASCs. We hypothesized that variation in any of these expansion conditions would influence the chondrogenic potential of ASCs. ASCs were isolated from human liposuction waste tissue and expanded through two passages with different tissue culture plastic, feed medium, and cell seeding densities. Once expanded, the cells were cast in an agarose gel and subjected to identical chondrogenic culture conditions for 7 days, at which point cell viability, radiolabel incorporation, and gene expression were measured. High rates of matrix synthesis upon chondrogenic induction were mostly associated with smaller cells, as indicated by cell width and area on tissue culture plastic, and it appears that expansion in a growth factor supplemented medium is important in maintaining this morphology. All end-point measures were highly dependent on the specific monolayer culture conditions. These results support the hypothesis that monolayer culture conditions may "prime" the cells or predispose them towards a specific phenotype and thus underscore the importance of early culture conditions in determining the growth and differentiation potential of ASCs.
脂肪来源干细胞(ASCs)是一种存在于脂肪组织中的丰富且易于获取的多能祖细胞群体。分离出的ASCs通常在含有10%胎牛血清的基础培养基中,于标准组织培养塑料上进行单层扩增。然而,最近的数据表明,通过使用悬浮培养塑料、向培养基中添加生长因子或调整接种密度来改变单层扩增条件,可能会影响ASCs的自我更新率、多能性和谱系特异性分化潜能。我们推测这些扩增条件中的任何一种变化都会影响ASCs的软骨生成潜能。从人类抽脂废弃组织中分离出ASCs,并通过在不同的组织培养塑料、培养基和细胞接种密度下进行两代扩增。扩增后,将细胞包埋在琼脂糖凝胶中,并在相同的软骨生成培养条件下培养7天,此时测量细胞活力、放射性标记掺入和基因表达。软骨生成诱导后基质合成的高比率大多与较小的细胞相关,这通过组织培养塑料上的细胞宽度和面积得以体现,并且似乎在补充生长因子的培养基中扩增对于维持这种形态很重要。所有终点测量结果都高度依赖于特定的单层培养条件。这些结果支持了这样的假设,即单层培养条件可能会“预处理”细胞或使它们倾向于特定的表型,从而强调了早期培养条件在决定ASCs的生长和分化潜能方面的重要性。