Gulp1 controls Eph/ephrin trogocytosis and is important for cell rearrangements during development

被引:19
作者
Gong, Jingyi [1 ]
Gaitanos, Thomas N. [1 ]
Luu, Olivia [2 ]
Huang, Yunyun [2 ]
Gaitanos, Louise [1 ]
Lindner, Jana [1 ]
Winklbauer, Rudolf [2 ]
Klein, Rudiger [1 ]
机构
[1] Max Planck Inst Neurobiol, Dept Mol Signaling Dev, Munich, Germany
[2] Univ Toronto, Dept Cell & Syst Biol, Toronto, ON, Canada
基金
加拿大自然科学与工程研究理事会; 加拿大健康研究院;
关键词
APOPTOTIC CELLS; BOUNDARY FORMATION; TRANS-ENDOCYTOSIS; RECEPTOR; INTERNALIZATION; PHAGOCYTOSIS; ENGULFMENT; EPHB2; AXON; MECHANISMS;
D O I
10.1083/jcb.201901032
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Trogocytosis, in which cells nibble away parts of neighboring cells, is an intercellular cannibalism process conserved from protozoa to mammals. Its underlying molecular mechanisms are not well understood and are likely distinct from phagocytosis, a process that clears entire cells. Bi-directional contact repulsion induced by Eph/ephrin signaling involves transfer of membrane patches and full-length Eph/ephrin protein complexes between opposing cells, resembling trogocytosis. Here, we show that the phagocytic adaptor protein Gulp1 regulates EphB/ephrinB trogocytosis to achieve efficient cell rearrangements of cultured cells and during embryonic development. Gulp1 mediates trogocytosis bi-directionally by dynamic engagement with EphB/ephrinB protein clusters in cooperation with the Rac-specific guanine nucleotide exchange factor Tiam2. Ultimately, Gulp1's presence at the Eph/ephrin cluster is a prerequisite for recruiting the endocytic GTPase dynamin. These results suggest that EphB/ephrinB trogocytosis, unlike other trogocytosis events, uses a phagocytosis-like mechanism to achieve efficient membrane scission and engulfment.
引用
收藏
页码:3455 / 3471
页数:17
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