Cross-talk between miR-471-5p and autophagy component proteins regulates LC3-associated phagocytosis (LAP) of apoptotic germ cells

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作者
Subbarayalu Panneerdoss
Suryavathi Viswanadhapalli
Nourhan Abdelfattah
Benjamin C. Onyeagucha
Santosh Timilsina
Tabrez A. Mohammad
Yidong Chen
Michael Drake
Kristiina Vuori
T. Rajendra Kumar
Manjeet K. Rao
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[1] University of Texas Health Science Center at San Antonio,Department of Cell Systems and Anatomy
[2] University of Texas Health Science Center at San Antonio,Greehey Children’s Cancer Research Institute 8403 Floyd Curl Drive
[3] University of Texas Health Science Center at San Antonio,Department of Obstetrics and Gynecology
[4] University of Texas Health Science Center at San Antonio,Department of Laboratory Animal Resources
[5] Sanford-Burnham Medical Research Institute,Department of Obstetrics and Gynecology
[6] University of Colorado Denver,undefined
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Phagocytic clearance of apoptotic germ cells by Sertoli cells is vital for germ cell development and differentiation. Here, using a tissue-specific miRNA transgenic mouse model, we show that interaction between miR-471-5p and autophagy member proteins regulates clearance of apoptotic germ cells via LC3-associated phagocytosis (LAP). Transgenic mice expressing miR-471-5p in Sertoli cells show increased germ cell apoptosis and compromised male fertility. Those effects are due to defective engulfment and impaired LAP-mediated clearance of apoptotic germ cells as miR-471-5p transgenic mice show lower levels of Dock180, LC3, Atg12, Becn1, Rab5 and Rubicon in Sertoli cells. Our results reveal that Dock180 interacts with autophagy member proteins to constitute a functional LC3-dependent phagocytic complex. We find that androgen regulates Sertoli cell phagocytosis by controlling expression of miR-471-5p and its target proteins. These findings suggest that recruitment of autophagy machinery is essential for efficient clearance of apoptotic germ cells by Sertoli cells using LAP.
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