Department of Pathology, Faculty of Medicine, Section of Oncopathology and Regenerative Biology, University of Miyazaki, 5200 Kihara, Kiyotake, Miyazaki 889-1692, Japan.
Hum Cell. 2012 Dec;25(4):100-10. doi: 10.1007/s13577-012-0055-2. Epub 2012 Dec 18.
Hepatocyte growth factor activator inhibitor type 1/serine protease inhibitor Kunitz type 1 (HAI-1/SPINT1) is a membrane-bound Kunitz-type serine protease inhibitor that is abundantly expressed on the surface of cytotrophoblasts, and is critically required for the formation of the placenta labyrinth in mice. HAI-1/SPINT1 regulates several membrane-associated cell surface serine proteases, with matriptase being the most cognate target. Matriptase degrades extracellular matrix protein such as laminin and activates other cell surface proteases including prostasin. This study aimed to analyze the role of HAI-1/SPINT1 in pericellular proteolysis of trophoblasts. In HAI-1/SPINT1-deficient mouse placenta, laminin immunoreactivity around trophoblasts was irregular and occasionally showed an intense punctate pattern, which differed significantly from the linear distribution along the basement membrane observed in wild-type placenta. To explore the molecular mechanism underlying this observation, we analyzed the effect of HAI-1/SPINT1 knock down (KD) on pericellular proteolysis in the human trophoblast cell line, BeWo. HAI-1/SPINT1-KD BeWo cells had increased amounts of cellular laminin protein and decreased laminin degradation activity in the culture supernatant. Subsequent analysis indicated that cell-associated matriptase was significantly decreased in KD cells whereas its mRNA level was not altered, suggesting an enhanced release and/or dislocation of matriptase in the absence of HAI-1/SPINT1. Moreover, prostasin activation and pericellular total serine protease activities were significantly suppressed by HAI-1/SPINT1 KD. These observations suggest that HAI-1/SPINT1 is critically required for the cell surface localization of matriptase in trophoblasts, and, in the absence of HAI-1/SPINT1, physiological activation of prostasin and other protease(s) initiated by cell surface matriptase may be impaired.
肝细胞生长因子激活物抑制剂 1/丝氨酸蛋白酶抑制剂 Kunitz 型 1(HAI-1/SPINT1)是一种膜结合的 Kunitz 型丝氨酸蛋白酶抑制剂,在滋养细胞表面大量表达,对于小鼠胎盘合体滋养层的形成至关重要。HAI-1/SPINT1 调节几种膜相关的细胞表面丝氨酸蛋白酶,其中以组织蛋白酶原激活物为最主要的靶标。组织蛋白酶原原激活物降解细胞外基质蛋白如层粘连蛋白,并激活其他细胞表面蛋白酶,包括前列腺蛋白酶原。本研究旨在分析 HAI-1/SPINT1 在滋养细胞细胞周蛋白水解中的作用。在 HAI-1/SPINT1 缺陷型小鼠胎盘中,滋养细胞周围的层粘连蛋白免疫反应性不规则,偶尔呈现强烈的点状模式,与野生型胎盘中观察到的沿着基膜的线性分布有显著差异。为了探讨这一观察结果的分子机制,我们分析了 HAI-1/SPINT1 敲低(KD)对人滋养细胞系 BeWo 细胞周蛋白水解的影响。HAI-1/SPINT1-KD BeWo 细胞的细胞内层粘连蛋白蛋白含量增加,培养上清中的层粘连蛋白降解活性降低。随后的分析表明,KD 细胞中细胞相关的组织蛋白酶原显著减少,但其 mRNA 水平没有改变,提示在没有 HAI-1/SPINT1 的情况下,组织蛋白酶原的释放和/或易位增强。此外,HAI-1/SPINT1 KD 显著抑制了前列腺蛋白酶原的激活和细胞周总丝氨酸蛋白酶活性。这些观察结果表明,HAI-1/SPINT1 对于滋养细胞表面组织蛋白酶原的定位至关重要,在没有 HAI-1/SPINT1 的情况下,可能会损害由细胞表面组织蛋白酶原引发的前列腺蛋白酶原和其他蛋白酶的生理激活。