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表达基质金属蛋白酶的细胞的入侵对于早期鸡胚胚盘原条的形成很重要。

Invasion by matrix metalloproteinase-expressing cells is important for primitive streak formation in early chick blastoderm.

机构信息

Research Institute for Integrated Sciences, Kanagawa University, Hiratsuka, Japan.

出版信息

Cells Tissues Organs. 2010;192(1):1-16. doi: 10.1159/000286231. Epub 2010 Feb 16.

Abstract

Epiblast cells in the early chick embryo differentiate to form all three germ layers through ingression of cells at the primitive streak across the basement membrane that underlies the epiblast. We tested the idea that degradation of the extracellular matrix components by matrix metalloproteinase(s) (MMPs) is involved in this process. Epiblast cells and primitive streak cells were dissociated into single cells and seeded onto a reconstituted basement membrane gel in vitro. Following overnight culture, approximately half the cells made holes in the substratum by dissolving the gel matrix. This invasive phenomenon was reproduced in vitro even when the cells were cultured upside down using a hanging culture system. We detected gelatinase activity in the culture supernatants from both prestreak epiblast cells and primitive streak cells. Pro-MMP-2 was detected in the culture media of the prestreak/streak cells as a 72-kDa band by gelatin zymography. In RT-PCR experiments, mRNAs for MMP-2, membrane-type (MT)3-MMP and MMP-11(stromelysin-3) were expressed in the epiblast cells before and during primitive streak formation. Injection of GM 6001 or other MMP inhibitors into the subgerminal cavity of the embryo inhibited the formation of the primitive streak and/or the primitive groove in more than 82% of the injected embryos. On the other hand, injection of a negative control compound instead of GM 6001 did not cause substantial inhibition. These results suggest that MMPs are involved in the enzymatic degradation of the basement membrane underlying the epiblast and are thus important for the ingression of mesendodermal cells along the primitive streak.

摘要

早期鸡胚的上胚层细胞通过穿过覆盖在上胚层的基底层的原始条纹中的细胞内陷,分化形成所有三个胚层。我们测试了这样一种观点,即细胞外基质成分的降解通过基质金属蛋白酶(MMPs)参与了这个过程。将上胚层细胞和原始条纹细胞分离成单细胞,并在体外接种到重建的基底膜凝胶上。过夜培养后,大约一半的细胞通过溶解凝胶基质在基质上打孔。即使使用悬挂培养系统将细胞倒置培养,这种侵袭现象也可以在体外重现。我们在预条纹上胚层细胞和原始条纹细胞的培养上清液中检测到明胶酶活性。通过明胶酶谱法,在预条纹/条纹细胞的培养基中检测到 pro-MMP-2 作为 72kDa 带。在 RT-PCR 实验中,在形成原始条纹之前和期间,MMP-2、膜型(MT)3-MMP 和 MMP-11(基质溶解素-3)的 mRNA 在上胚层细胞中表达。将 GM 6001 或其他 MMP 抑制剂注入胚胎的亚生殖腔中,可使超过 82%的注射胚胎中原始条纹和/或原始沟的形成受到抑制。另一方面,注射阴性对照化合物而不是 GM 6001 不会导致明显的抑制。这些结果表明 MMPs 参与了覆盖在上胚层的基底层的酶降解,因此对于中胚层和内胚层细胞沿着原始条纹的内陷是重要的。

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