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乳脂肪球表皮生长因子8调控的凋亡颗粒细胞吞噬机制

Phagocytosis mechanism of apoptotic granulosa cells regulated by milk-fat globule-EGF factor 8.

作者信息

Naka Mayumi, Kusakabe Ken, Takeshita Ai, Nakagawa Hiroshi, Ito Yuko, Shibata Masa-Aki, Otsuki Yoshinori

机构信息

Department of Anatomy and Cell Biology, Division of Life Sciences, Osaka Medical College, Takatsuki, Osaka 569-8686, Japan.

出版信息

Med Mol Morphol. 2009 Sep;42(3):143-9. doi: 10.1007/s00795-009-0452-0. Epub 2009 Sep 26.

Abstract

In the process of ovary sexual maturation, most immature ovarian follicles degrade into atretic follicles accompanied by apoptosis in granulosa cells. Macrophages can recognize apoptotic cells through specific binding with phosphatidylserine (PS), exposed on the surface of apoptotic cells, which is mediated by milk-fat globule-EGF factor 8 (MFG-E8). In the present research, we examined the involvement of the MFG-E8-dependent phagocytosis system in the atretic follicles of developing mouse ovaries. The number of atretic follicles and DNA-fragmented granulosa cells significantly increased in B6C3F1 mice during 2 to 6 weeks. Chromatin-condensed granulosa cells were engulfed by macrophages, which existed in the stroma or atretic follicles, or by neighboring normal granulosa cells. MFG-E8 mRNA increased in ovaries during 2 to 6 weeks, and immunoreactivity of MFG-E8 was detected at the surface of apoptotic cells existing around the antrum. Immunoelectron microscopic study revealed MFG-E8-positive signals on the membrane of apoptotic cells near macrophages, but apoptotic cells engulfed by neighboring granulosa cells showed few signals. Anti-Fas antibody elevated the annexin-V-positive reaction in isolated granulosa cells from 3-week-old mouse ovaries. MFG-E8 seems to act on the phagocytosis of apoptotic granulosa cells via macrophages and contribute to the regression process of atretic follicles.

摘要

在卵巢性成熟过程中,大多数未成熟的卵巢卵泡会退化形成闭锁卵泡,同时颗粒细胞会发生凋亡。巨噬细胞可通过与凋亡细胞表面暴露的磷脂酰丝氨酸(PS)特异性结合来识别凋亡细胞,这一过程由乳脂肪球表皮生长因子8(MFG-E8)介导。在本研究中,我们检测了MFG-E8依赖的吞噬系统在发育中小鼠卵巢闭锁卵泡中的作用。在2至6周龄期间,B6C3F1小鼠的闭锁卵泡数量和DNA片段化的颗粒细胞显著增加。染色质浓缩的颗粒细胞被存在于基质或闭锁卵泡中的巨噬细胞或相邻的正常颗粒细胞吞噬。在2至6周龄期间,卵巢中MFG-E8 mRNA增加,并且在卵泡腔周围存在的凋亡细胞表面检测到MFG-E8的免疫反应性。免疫电子显微镜研究显示,巨噬细胞附近凋亡细胞的膜上有MFG-E8阳性信号,但被相邻颗粒细胞吞噬的凋亡细胞显示的信号较少。抗Fas抗体可提高从3周龄小鼠卵巢分离的颗粒细胞中膜联蛋白V阳性反应。MFG-E8似乎通过巨噬细胞作用于凋亡颗粒细胞的吞噬,并有助于闭锁卵泡的退化过程。

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