Children's Hospital, Boston, USA.
Matrix Biol. 2010 Jan;29(1):3-8. doi: 10.1016/j.matbio.2009.09.003. Epub 2009 Sep 17.
Previously, we described a profound impact of structural conformation of collagen matrix on osteogenic and adipogenic differentiation of bone marrow stromal cells. Thus, a marginal p38-independent adipogenesis on native collagen I matrix contrasts with an efficient p38-dependent differentiation on denatured collagen I. An efficient Hsp90-dependent osteogenesis occurs on native collagen I matrix but not on its denatured counterpart where it is insignificant and proceeds in an Hsp90-independent manner. Whereas only marginal osteogenesis and no detectable adipogenesis of bone marrow stromal cells occur on native collagen IV, the same matrix supports a highly efficient adipogenesis in denatured structural state. The present study addresses the opposite direction in the flow of cell-matrix interaction, namely the cells' influence on structural state of collagen matrix, and tests the possibility that differentiating bone marrow stromal cells may adjust the expression phenotype of MMP and TIMP in such a way that, if translated into matrix modification, would facilitate the maintenance of collagen matrix in or its modification into structural state optimal for the ongoing differentiation process. The results obtained indicate that this is indeed the case. In bone marrow stromal cells stimulated to undergo adipogenesis the expression of MMP increases and that of TIMP decreases. In cells induced to undergo osteogenesis the opposite is true: MMP/TIMP expression is adjusted in a manner that, if translated into matrix modification, could promote the native structural conformation optimal for this type of differentiation. The results obtained also indicate that the observed adjustment in MMP/TIMP expression phenotype might be an early differentiation event and that differentiation stimulation alone might be sufficient to trigger it even on matrices not favorable to a given type of differentiation. The findings of the present study raise significant questions and indicate directions for further experimentation.
先前,我们描述了胶原基质的结构构象对骨髓基质细胞成骨和脂肪生成分化的深远影响。因此,天然胶原 I 基质上的边缘化 p38 非依赖性脂肪生成与变性胶原 I 上的有效 p38 依赖性分化形成鲜明对比。天然胶原 I 基质上发生有效的 Hsp90 依赖性成骨作用,但在其变性对应物上则不明显且以 Hsp90 非依赖性方式进行。尽管骨髓基质细胞在天然胶原 IV 上仅发生边缘化成骨作用而无可检测到的脂肪生成作用,但相同的基质在变性结构状态下支持高效的脂肪生成作用。本研究探讨了细胞-基质相互作用的相反方向,即细胞对胶原基质结构状态的影响,并测试了分化的骨髓基质细胞可能通过何种方式调整 MMP 和 TIMP 的表达表型,以便如果转化为基质修饰,则有利于胶原基质的维持或其修饰成适合正在进行的分化过程的结构状态。所得结果表明情况确实如此。在被刺激进行脂肪生成的骨髓基质细胞中,MMP 的表达增加,而 TIMP 的表达减少。在被诱导进行成骨的细胞中则相反:MMP/TIMP 的表达被调整为,如果转化为基质修饰,则可以促进适合这种分化类型的天然结构构象。所得结果还表明,观察到的 MMP/TIMP 表达表型的调整可能是早期分化事件,并且仅分化刺激本身就足以在不适合特定类型分化的基质上引发该事件。本研究的发现提出了重要的问题,并为进一步的实验指明了方向。