Mfge8 is critical for mammary gland remodeling during involution

被引:85
作者
Atabai, K
Fernandez, R
Huang, XZ
Ueki, I
Kline, A
Li, Y
Sadatmansoori, S
Smith-Steinhart, C
Zhu, WM
Pytela, R
Werb, Z
Sheppard, D [1 ]
机构
[1] Univ Calif San Francisco, Lung Biol Ctr, Inst Cardiovasc Res, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Med, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Dept Anat, San Francisco, CA 94143 USA
[4] Univ Colorado, Hlth Sci Ctr, Dept Immunol, Denver, CO 80206 USA
[5] Univ Colorado, Hlth Sci Ctr, Natl Jewish Med Ctr, Denver, CO 80206 USA
[6] Univ Colorado, Hlth Sci Ctr, Dept Med, Denver, CO 80206 USA
[7] Epitomics, Burlingame, CA 94010 USA
关键词
D O I
10.1091/mbc.E05-02-0128
中图分类号
Q2 [细胞生物学];
学科分类号
071009 [细胞生物学]; 090102 [作物遗传育种];
摘要
Apoptosis is a critical process in normal mammary gland development and the rapid clearance of apoptotic cells prevents tissue injury associated with the release of intracellular antigens from dying cells. Milk fat globule-EGF-factor 8 (Mfge8) is a milk glycoprotein that is abundantly expressed in the mammary gland epithelium and has been shown to facilitate the clearance of apoptotic lymphocytes by splenic macrophages. We report that mice with disruption of Mfge8 had normal mammary gland development until involution. However, abnormal mammary gland remodeling was observed postlactation in Mfge8 mutant mice. During early involution, Mfge8 mutant mice had increased numbers of apoptotic cells within the mammary gland associated with a delay in alveolar collapse and fat cell repopulation. As involution progressed, Mfge8 mutants developed inflammation as assessed by CD45 and CD11b staining of mammary gland tissue sections. With additional pregnancies, Mfge8 mutant mice developed progressive dilatation of the mammary gland ductal network. These data demonstrate that Mfge8 regulates the clearance of apoptotic epithelial cells during mammary gland involution and that the absence of Mfge8 leads to inflammation and abnormal mammary gland remodeling.
引用
收藏
页码:5528 / 5537
页数:10
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