Semantic Scholar Open Access 2013 43 sitasi

Clathrin and AP2 Are Required for Phagocytic Receptor-Mediated Apoptotic Cell Clearance in Caenorhabditis elegans

Didi Chen Y. Jian Xuezhao Liu Yuanya Zhang Jingjing Liang +9 lainnya

Abstrak

Clathrin and the multi-subunit adaptor protein complex AP2 are central players in clathrin-mediated endocytosis by which the cell selectively internalizes surface materials. Here, we report the essential role of clathrin and AP2 in phagocytosis of apoptotic cells. In Caenorhabditis elegans, depletion of the clathrin heavy chain CHC-1 and individual components of AP2 led to a significant accumulation of germ cell corpses, which resulted from defects in both cell corpse engulfment and phagosome maturation required for corpse removal. CHC-1 and AP2 components associate with phagosomes in an inter-dependent manner. Importantly, we found that the phagocytic receptor CED-1 interacts with the α subunit of AP2, while the CED-6/Gulp adaptor forms a complex with both CHC-1 and the AP2 complex, which likely mediates the rearrangement of the actin cytoskeleton required for cell corpse engulfment triggered by the CED-1 signaling pathway. In addition, CHC-1 and AP2 promote the phagosomal association of LST-4/Snx9/18/33 and DYN-1/dynamin by forming a complex with them, thereby facilitating the maturation of phagosomes necessary for corpse degradation. These findings reveal a non-classical role of clathrin and AP2 and establish them as indispensable regulators in phagocytic receptor-mediated apoptotic cell clearance.

Topik & Kata Kunci

Penulis (14)

D

Didi Chen

Y

Y. Jian

X

Xuezhao Liu

Y

Yuanya Zhang

J

Jingjing Liang

X

Xiaying Qi

H

Hongwei Du

W

Wei Zou

L

Lianwan Chen

Y

Yongping Chai

G

Guangshuo Ou

L

Long Miao

Y

Yingchun Wang

C

Chonglin Yang

Format Sitasi

Chen, D., Jian, Y., Liu, X., Zhang, Y., Liang, J., Qi, X. et al. (2013). Clathrin and AP2 Are Required for Phagocytic Receptor-Mediated Apoptotic Cell Clearance in Caenorhabditis elegans. https://doi.org/10.1371/journal.pgen.1003517

Akses Cepat

Informasi Jurnal
Tahun Terbit
2013
Bahasa
en
Total Sitasi
43×
Sumber Database
Semantic Scholar
DOI
10.1371/journal.pgen.1003517
Akses
Open Access ✓