Integrin α PAT-2/CDC-42 signaling is required for muscle-mediated clearance of apoptotic cells in Caenorhabditis elegans.

Clearance of apoptotic cells by engulfment plays an important role in the homeostasis and development of multicellular organisms. Despite the fact that the recognition of apoptotic cells by engulfment receptors is critical in inducing the engulfment process, the molecular mechanisms are still poorly...

Full description

Bibliographic Details
Main Authors: Hsiao-Han Hsieh, Tsung-Yuan Hsu, Hang-Shiang Jiang, Yi-Chun Wu
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS Genetics
Online Access:http://europepmc.org/articles/PMC3355063?pdf=render
_version_ 1818456949673426944
author Hsiao-Han Hsieh
Tsung-Yuan Hsu
Hang-Shiang Jiang
Yi-Chun Wu
author_facet Hsiao-Han Hsieh
Tsung-Yuan Hsu
Hang-Shiang Jiang
Yi-Chun Wu
author_sort Hsiao-Han Hsieh
collection DOAJ
description Clearance of apoptotic cells by engulfment plays an important role in the homeostasis and development of multicellular organisms. Despite the fact that the recognition of apoptotic cells by engulfment receptors is critical in inducing the engulfment process, the molecular mechanisms are still poorly understood. Here, we characterize a novel cell corpse engulfment pathway mediated by the integrin α subunit PAT-2 in Caenorhabditis elegans and show that it specifically functions in muscle-mediated engulfment during embryogenesis. Inactivation of pat-2 results in a defect in apoptotic cell internalization. The PAT-2 extracellular region binds to the surface of apoptotic cells in vivo, and the intracellular region may mediate signaling for engulfment. We identify essential roles of small GTPase CDC-42 and its activator UIG-1, a guanine-nucleotide exchange factor, in PAT-2-mediated cell corpse removal. PAT-2 and CDC-42 both function in muscle cells for apoptotic cell removal and are co-localized in growing muscle pseudopods around apoptotic cells. Our data suggest that PAT-2 functions through UIG-1 for CDC-42 activation, which in turn leads to cytoskeletal rearrangement and apoptotic cell internalization by muscle cells. Moreover, in contrast to PAT-2, the other integrin α subunit INA-1 and the engulfment receptor CED-1, which signal through the conserved signaling molecules CED-5 (DOCK180)/CED-12 (ELMO) or CED-6 (GULP) respectively, preferentially act in epithelial cells to mediate cell corpse removal during mid-embryogenesis. Our results show that different engulfing cells utilize distinct repertoires of receptors for engulfment at the whole organism level.
first_indexed 2024-12-14T22:34:48Z
format Article
id doaj.art-5383831b75e14a2386dd4189406b4271
institution Directory Open Access Journal
issn 1553-7390
1553-7404
language English
last_indexed 2024-12-14T22:34:48Z
publishDate 2012-01-01
publisher Public Library of Science (PLoS)
record_format Article
series PLoS Genetics
spelling doaj.art-5383831b75e14a2386dd4189406b42712022-12-21T22:45:10ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042012-01-0185e100266310.1371/journal.pgen.1002663Integrin α PAT-2/CDC-42 signaling is required for muscle-mediated clearance of apoptotic cells in Caenorhabditis elegans.Hsiao-Han HsiehTsung-Yuan HsuHang-Shiang JiangYi-Chun WuClearance of apoptotic cells by engulfment plays an important role in the homeostasis and development of multicellular organisms. Despite the fact that the recognition of apoptotic cells by engulfment receptors is critical in inducing the engulfment process, the molecular mechanisms are still poorly understood. Here, we characterize a novel cell corpse engulfment pathway mediated by the integrin α subunit PAT-2 in Caenorhabditis elegans and show that it specifically functions in muscle-mediated engulfment during embryogenesis. Inactivation of pat-2 results in a defect in apoptotic cell internalization. The PAT-2 extracellular region binds to the surface of apoptotic cells in vivo, and the intracellular region may mediate signaling for engulfment. We identify essential roles of small GTPase CDC-42 and its activator UIG-1, a guanine-nucleotide exchange factor, in PAT-2-mediated cell corpse removal. PAT-2 and CDC-42 both function in muscle cells for apoptotic cell removal and are co-localized in growing muscle pseudopods around apoptotic cells. Our data suggest that PAT-2 functions through UIG-1 for CDC-42 activation, which in turn leads to cytoskeletal rearrangement and apoptotic cell internalization by muscle cells. Moreover, in contrast to PAT-2, the other integrin α subunit INA-1 and the engulfment receptor CED-1, which signal through the conserved signaling molecules CED-5 (DOCK180)/CED-12 (ELMO) or CED-6 (GULP) respectively, preferentially act in epithelial cells to mediate cell corpse removal during mid-embryogenesis. Our results show that different engulfing cells utilize distinct repertoires of receptors for engulfment at the whole organism level.http://europepmc.org/articles/PMC3355063?pdf=render
spellingShingle Hsiao-Han Hsieh
Tsung-Yuan Hsu
Hang-Shiang Jiang
Yi-Chun Wu
Integrin α PAT-2/CDC-42 signaling is required for muscle-mediated clearance of apoptotic cells in Caenorhabditis elegans.
PLoS Genetics
title Integrin α PAT-2/CDC-42 signaling is required for muscle-mediated clearance of apoptotic cells in Caenorhabditis elegans.
title_full Integrin α PAT-2/CDC-42 signaling is required for muscle-mediated clearance of apoptotic cells in Caenorhabditis elegans.
title_fullStr Integrin α PAT-2/CDC-42 signaling is required for muscle-mediated clearance of apoptotic cells in Caenorhabditis elegans.
title_full_unstemmed Integrin α PAT-2/CDC-42 signaling is required for muscle-mediated clearance of apoptotic cells in Caenorhabditis elegans.
title_short Integrin α PAT-2/CDC-42 signaling is required for muscle-mediated clearance of apoptotic cells in Caenorhabditis elegans.
title_sort integrin α pat 2 cdc 42 signaling is required for muscle mediated clearance of apoptotic cells in caenorhabditis elegans
url http://europepmc.org/articles/PMC3355063?pdf=render
work_keys_str_mv AT hsiaohanhsieh integrinapat2cdc42signalingisrequiredformusclemediatedclearanceofapoptoticcellsincaenorhabditiselegans
AT tsungyuanhsu integrinapat2cdc42signalingisrequiredformusclemediatedclearanceofapoptoticcellsincaenorhabditiselegans
AT hangshiangjiang integrinapat2cdc42signalingisrequiredformusclemediatedclearanceofapoptoticcellsincaenorhabditiselegans
AT yichunwu integrinapat2cdc42signalingisrequiredformusclemediatedclearanceofapoptoticcellsincaenorhabditiselegans