Icardo J M, Nakamura A, Fernandez-Teran M A, Manasek F J
Department of Anatomy and Cell Biology, University of Cantabria, Faculty of Medicine, Santander, Spain.
Anat Embryol (Berl). 1992;185(3):239-47. doi: 10.1007/BF00211822.
During heart development in the chick some of the endocardial cells that cover the cushion areas leave the cushion endocardium, seed the underlying cardiac jelly, and are transformed into mesenchyme. Cushion mesenchymal (CM) cells migrate from the endocardium toward the myocardium using the cardiac jelly as substratum. Developing cushions have been microinjected with fibronectin (FN), antifibronectin antibodies (AbFN), and four synthetic peptide probes. Two of these peptides (P7 and P10) contained the sequence Arg-Gly-Asp-Ser (RGDS), while the other two (P15 and PColl) did not. Cushion area, individual cell area, cell density, cell orientation and a factor of form were evaluated in both experimental and control cushions. CM cell migration was inhibited by FN and AbFN, only partially inhibited by P10 and unaffected by P7. Cushions injected with P15 and PColl were unaffected. These results can be explained by steric modifications of the extracellular matrix, that may render cardiac jelly nonpermissive for CM cell migration, or by interaction of the substances injected at the endocardial cell surface. Migrating CM cells do not present any preferential orientation in any particular direction. CM cell migration seems to depend upon intrinsic migratory behaviour and the presence of FN at the CM cell surface. The enforcement of the direction of CM cell migration does not appear to rely upon matrix signals but be the result of randomly migrating cells becoming distributed more evenly in the matrix.
在鸡心脏发育过程中,覆盖垫状区域的一些心内膜细胞离开垫状心内膜,植入下方的心脏胶样物,并转化为间充质。垫状间充质(CM)细胞以心脏胶样物为基质,从心内膜向心肌迁移。已将纤连蛋白(FN)、抗纤连蛋白抗体(AbFN)和四种合成肽探针显微注射到发育中的垫状组织中。其中两种肽(P7和P10)含有精氨酸 - 甘氨酸 - 天冬氨酸 - 丝氨酸(RGDS)序列,而另外两种(P15和PColl)则没有。对实验性和对照性垫状组织的垫状区域、单个细胞面积、细胞密度、细胞取向和形态因子进行了评估。CM细胞迁移受到FN和AbFN的抑制,仅部分受到P10的抑制,而不受P7的影响。注射P15和PColl的垫状组织未受影响。这些结果可以通过细胞外基质的空间修饰来解释,这可能使心脏胶样物不利于CM细胞迁移,或者通过在内皮细胞表面注射的物质之间的相互作用来解释。迁移的CM细胞在任何特定方向上都没有呈现出任何优先取向。CM细胞迁移似乎取决于内在的迁移行为以及CM细胞表面FN的存在。CM细胞迁移方向的强化似乎不依赖于基质信号,而是随机迁移的细胞在基质中分布更均匀的结果。