Gulp1 controls Eph/ephrin trogocytosis and is important for cell rearrangements during development
Author(s) -
Jingyi Gong,
Thomas N. Gaitanos,
Olivia Luu,
Yunyun Huang,
Louise Gaitanos,
Jana Lindner,
Rudolf Winklbauer,
Rüdiger Klein
Publication year - 2019
Publication title -
the journal of cell biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.414
H-Index - 380
eISSN - 1540-8140
pISSN - 0021-9525
DOI - 10.1083/jcb.201901032
Subject(s) - erythropoietin producing hepatocellular (eph) receptor , ephrin , microbiology and biotechnology , biology , endocytic cycle , signal transducing adaptor protein , guanine nucleotide exchange factor , endocytosis , embryonic stem cell , signal transduction , cell , genetics , gene , receptor tyrosine kinase
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.
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