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The Core Molecular Machinery Used for Engulfment of Apoptotic Cells Regulates the JNK Pathway Mediating Axon Regeneration in Caenorhabditis elegans
被引:18
|作者:
Pastuhov, Strahil Iv.
[1
]
Fujiki, Kota
[1
]
Tsuge, Anna
[1
]
Asai, Kazuma
[1
]
Ishikawa, Sho
[1
]
Hirose, Kazuya
[1
]
Matsumoto, Kunihiro
[1
]
Hisamoto, Naoki
[1
]
机构:
[1] Nagoya Univ, Grad Sch Sci, Div Biol Sci, Chikusa Ku, Nagoya, Aichi 4648602, Japan
基金:
日本学术振兴会;
关键词:
axon regeneration;
C;
elegans;
Rac;
signal transduction;
KINASE SIGNALING PATHWAY;
C;
ELEGANS;
CRKII/DOCK180/RAC PATHWAY;
CORPSE ENGULFMENT;
STRESS-RESPONSE;
PHAGOCYTOSIS;
MIGRATION;
PROTEIN;
REQUIRES;
RECEPTOR;
D O I:
10.1523/JNEUROSCI.0453-16.2016
中图分类号:
Q189 [神经科学];
学科分类号:
071006 ;
摘要:
The mechanisms that govern the ability of specific neurons to regenerate their axons after injury are not well understood. In Caenorhabditis elegans, the initiation of axon regeneration is positively regulated by the JNK-MAPK pathway. In this study, we identify two components functioning upstream of the JNK pathway: the Ste20-related protein kinase MAX-2 and the Rac-type GTPase CED-10. CED-10, when bound by GTP, interacts with MAX-2 and functions as its upstream regulator in axon regeneration. CED-10, in turn, is activated by axon injury via signals initiated from the integrin alpha-subunit INA-1 and the nonreceptor tyrosine kinase SRC-1 and transmitted via the signaling module CED-2/CrkII-CED-5/Dock180-CED-12/ELMO. This module is also known to regulate the engulfment of apoptotic cells during development. Our findings thus reveal that the molecular machinery used for engulfment of apoptotic cells also promotes axon regeneration through activation of the JNK pathway.
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页码:9710 / 9721
页数:12
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