Phosphatidylserine exposure mediated by ABC transporter activates the integrin signaling pathway promoting axon regeneration

被引:27
|
作者
Hisamoto, Naoki [1 ]
Tsuge, Anna [1 ]
Pastuhov, Strahil Iv [1 ]
Shimizu, Tatsuhiro [1 ]
Hanafusa, Hiroshi [1 ]
Matsumoto, Kunihiro [1 ]
机构
[1] Nagoya Univ, Grad Sch Sci, Div Biol Sci, Chikusa Ku, Nagoya, Aichi 4648602, Japan
来源
NATURE COMMUNICATIONS | 2018年 / 9卷
关键词
CAENORHABDITIS-ELEGANS; APOPTOTIC CELLS; C; ELEGANS; EAT-ME; ENGULFMENT; REQUIRES; CASPASES; CED-7; P38;
D O I
10.1038/s41467-018-05478-w
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Following axon injury, a cascade of signaling events is triggered to initiate axon regeneration. However, the mechanisms regulating axon regeneration are not well understood at present. In Caenorhabditis elegans, axon regeneration utilizes many of the components involved in phagocytosis, including integrin and Rac GTPase. Here, we identify the transthyretin (TTR)-like protein TTR-11 as a component functioning in axon regeneration upstream of integrin. We show that TTR-11 binds to both the extracellular domain of integrin-alpha and phosphatidylserine (PS). Axon injury induces the accumulation of PS around the injured axons in a manner dependent on TTR-11, the ABC transporter CED-7, and the caspase CED-3. Furthermore, we demonstrate that CED-3 activates CED-7 during axon regeneration. Thus, TTR-11 functions to link the PS injury signal to activation of the integrin pathway, which then initiates axon regeneration.
引用
收藏
页数:11
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