Nakatani Hajime, Aoki Naohito, Nakagawa Yoshimi, Jin-No Shinji, Aoyama Koji, Oshima Kenji, Ohira Sachiyo, Sato Chihiro, Nadano Daita, Matsuda Tsukasa
Department of Applied Molecular Biosciences, Graduate School of Bioagricultural Sciences, Nagoya University, Furo-cho, Chikusa-ku, Nagoya 464-8601, Japan.
Biochem J. 2006 Apr 1;395(1):21-30. doi: 10.1042/BJ20051459.
A milk membrane glycoprotein, MFG-E8 [milk fat globule-EGF (epidermal growth factor) factor 8], is expressed abundantly in lactating mammary glands in stage- and tissue-specific manners, and has been believed to be secreted in association with milk fat globules. In the present paper, we describe further up-regulation of MFG-E8 in involuting mammary glands, where the glands undergo a substantial increase in the rate of epithelial cell apoptosis, and a possible role of MFG-E8 in mediating recognition and engulfment of apoptotic cells through its specific binding to PS (phosphatidylserine). Immunoblotting and RNA blotting analyses revealed that both MFG-E8 protein and MFG-E8 mRNA were markedly increased in mammary tissue within 3 days of either natural or forced weaning (pup withdrawal) of lactating mice. Using immunohistochemical analysis of the mammary tissue cryosections, the MFG-E8 signal was detected around the epithelium of such involuting mammary glands, but was almost undetectable at early- and mid-lactation stages, although strong signals were obtained for milk fat globules stored in the alveolar lumen. Some signals double positive to a macrophage differentiation marker, CD68, and MFG-E8 were detected in the post-weaning mammary tissue, although such double-positive signals were much smaller in number than the MFG-E8 single-positive ones. Total MFG-E8 in milk was also increased in the post-weaning mammary glands and, furthermore, the free MFG-E8 content in the post-weaning milk, as measured by in vitro PS-binding and apoptotic HC11 cell-binding activities, was much higher than that of lactation. In addition, the post-weaning milk enhanced the binding of apoptotic HC11 cells to J774 macrophages. Sucrose density-gradient ultracentrifugation analyses revealed that such enhanced PS-binding activity of MFG-E8 was present in membrane vesicle fractions (density 1.05-1.13 g/ml), rather than milk fat globule fractions. The weaning-induced MFG-E8 might play an important role in the recognition and engulfment of apoptotic epithelial cells by the neighbouring phagocytic epithelial cells in involuting mammary glands.
一种乳膜糖蛋白,即乳脂肪球-表皮生长因子8(MFG-E8),在泌乳期乳腺中以阶段和组织特异性方式大量表达,并且一直被认为是与乳脂肪球相关联分泌的。在本文中,我们描述了在退化期乳腺中MFG-E8的进一步上调,此时乳腺上皮细胞凋亡率大幅增加,以及MFG-E8通过其与磷脂酰丝氨酸(PS)的特异性结合在介导凋亡细胞的识别和吞噬中的可能作用。免疫印迹和RNA印迹分析显示,在泌乳小鼠自然或强制断奶(幼崽撤离)3天内,乳腺组织中的MFG-E8蛋白和MFG-E8 mRNA均显著增加。通过对乳腺组织冰冻切片进行免疫组织化学分析,在这种退化期乳腺的上皮周围检测到MFG-E8信号,但在泌乳早期和中期几乎检测不到,尽管在肺泡腔中储存的乳脂肪球获得了强信号。在断奶后的乳腺组织中检测到一些与巨噬细胞分化标志物CD68和MFG-E8双阳性的信号,尽管这种双阳性信号的数量比MFG-E8单阳性信号少得多。断奶后乳腺中乳中的总MFG-E8也增加了,此外,通过体外PS结合和凋亡HC11细胞结合活性测量,断奶后乳中游离MFG-E8的含量远高于泌乳期。此外,断奶后的乳增强了凋亡HC11细胞与J774巨噬细胞的结合。蔗糖密度梯度超速离心分析显示,MFG-E8这种增强的PS结合活性存在于膜泡组分(密度1.05 - 1.13 g/ml)中,而不是乳脂肪球组分中。断奶诱导的MFG-E8可能在退化期乳腺中相邻吞噬性上皮细胞识别和吞噬凋亡上皮细胞中起重要作用。