Cargando…

Sonic Hedgehog acts as a macrophage chemoattractant during regeneration of the gastric epithelium

Sonic Hedgehog (Shh), secreted from gastric parietal cells, contributes to the regeneration of the epithelium. The recruitment of macrophages plays a central role in the regenerative process. The mechanism that regulates macrophage recruitment in response to gastric injury is largely unknown. Here w...

Descripción completa

Detalles Bibliográficos
Autores principales: Chakrabarti, Jayati, Dua-Awereh, Martha, Schumacher, Michael, Engevik, Amy, Hawkins, Jennifer, Helmrath, Michael A., Zavros, Yana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8755719/
https://www.ncbi.nlm.nih.gov/pubmed/35022438
http://dx.doi.org/10.1038/s41536-021-00196-2
_version_ 1784632429421527040
author Chakrabarti, Jayati
Dua-Awereh, Martha
Schumacher, Michael
Engevik, Amy
Hawkins, Jennifer
Helmrath, Michael A.
Zavros, Yana
author_facet Chakrabarti, Jayati
Dua-Awereh, Martha
Schumacher, Michael
Engevik, Amy
Hawkins, Jennifer
Helmrath, Michael A.
Zavros, Yana
author_sort Chakrabarti, Jayati
collection PubMed
description Sonic Hedgehog (Shh), secreted from gastric parietal cells, contributes to the regeneration of the epithelium. The recruitment of macrophages plays a central role in the regenerative process. The mechanism that regulates macrophage recruitment in response to gastric injury is largely unknown. Here we tested the hypothesis that Shh stimulates macrophage chemotaxis to the injured epithelium and contributes to gastric regeneration. A mouse model expressing a myeloid cell-specific deletion of Smoothened (LysMcre/+;Smof/f) was generated using transgenic mice bearing loxP sites flanking the Smo gene (Smo loxP) and mice expressing a Cre recombinase transgene from the Lysozyme M locus (LysMCre). Acetic acid injury was induced in the stomachs of both control and LysMcre/+;Smof/f (SmoKO) mice and gastric epithelial regeneration and macrophage recruitment analyzed over a period of 7 days post-injury. Bone marrow-derived macrophages (BM-Mø) were collected from control and SmoKO mice. Human-derived gastric organoid/macrophage co-cultures were established, and macrophage chemotaxis measured. Compared to control mice, SmoKO animals exhibited inhibition of ulcer repair and normal epithelial regeneration, which correlated with decreased macrophage infiltration at the site of injury. Bone marrow chimera experiments using SmoKO donor cells showed that control chimera mice transplanted with SmoKO bone marrow donor cells exhibited a loss of ulcer repair, and transplantation of control bone marrow donor cells to SmoKO mice rescued epithelial cell regeneration. Histamine-stimulated Shh secretion in human organoid/macrophage co-cultures resulted in macrophage migration toward the gastric epithelium, a response that was blocked with Smo inhibitor Vismodegib. Shh-induced macrophage migration was mediated by AKT signaling. In conclusion, Shh signaling acts as a macrophage chemoattractant via a Smo-dependent mechanism during gastric epithelial regeneration in response to injury.
format Online
Article
Text
id pubmed-8755719
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-87557192022-01-20 Sonic Hedgehog acts as a macrophage chemoattractant during regeneration of the gastric epithelium Chakrabarti, Jayati Dua-Awereh, Martha Schumacher, Michael Engevik, Amy Hawkins, Jennifer Helmrath, Michael A. Zavros, Yana NPJ Regen Med Article Sonic Hedgehog (Shh), secreted from gastric parietal cells, contributes to the regeneration of the epithelium. The recruitment of macrophages plays a central role in the regenerative process. The mechanism that regulates macrophage recruitment in response to gastric injury is largely unknown. Here we tested the hypothesis that Shh stimulates macrophage chemotaxis to the injured epithelium and contributes to gastric regeneration. A mouse model expressing a myeloid cell-specific deletion of Smoothened (LysMcre/+;Smof/f) was generated using transgenic mice bearing loxP sites flanking the Smo gene (Smo loxP) and mice expressing a Cre recombinase transgene from the Lysozyme M locus (LysMCre). Acetic acid injury was induced in the stomachs of both control and LysMcre/+;Smof/f (SmoKO) mice and gastric epithelial regeneration and macrophage recruitment analyzed over a period of 7 days post-injury. Bone marrow-derived macrophages (BM-Mø) were collected from control and SmoKO mice. Human-derived gastric organoid/macrophage co-cultures were established, and macrophage chemotaxis measured. Compared to control mice, SmoKO animals exhibited inhibition of ulcer repair and normal epithelial regeneration, which correlated with decreased macrophage infiltration at the site of injury. Bone marrow chimera experiments using SmoKO donor cells showed that control chimera mice transplanted with SmoKO bone marrow donor cells exhibited a loss of ulcer repair, and transplantation of control bone marrow donor cells to SmoKO mice rescued epithelial cell regeneration. Histamine-stimulated Shh secretion in human organoid/macrophage co-cultures resulted in macrophage migration toward the gastric epithelium, a response that was blocked with Smo inhibitor Vismodegib. Shh-induced macrophage migration was mediated by AKT signaling. In conclusion, Shh signaling acts as a macrophage chemoattractant via a Smo-dependent mechanism during gastric epithelial regeneration in response to injury. Nature Publishing Group UK 2022-01-12 /pmc/articles/PMC8755719/ /pubmed/35022438 http://dx.doi.org/10.1038/s41536-021-00196-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Chakrabarti, Jayati
Dua-Awereh, Martha
Schumacher, Michael
Engevik, Amy
Hawkins, Jennifer
Helmrath, Michael A.
Zavros, Yana
Sonic Hedgehog acts as a macrophage chemoattractant during regeneration of the gastric epithelium
title Sonic Hedgehog acts as a macrophage chemoattractant during regeneration of the gastric epithelium
title_full Sonic Hedgehog acts as a macrophage chemoattractant during regeneration of the gastric epithelium
title_fullStr Sonic Hedgehog acts as a macrophage chemoattractant during regeneration of the gastric epithelium
title_full_unstemmed Sonic Hedgehog acts as a macrophage chemoattractant during regeneration of the gastric epithelium
title_short Sonic Hedgehog acts as a macrophage chemoattractant during regeneration of the gastric epithelium
title_sort sonic hedgehog acts as a macrophage chemoattractant during regeneration of the gastric epithelium
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8755719/
https://www.ncbi.nlm.nih.gov/pubmed/35022438
http://dx.doi.org/10.1038/s41536-021-00196-2
work_keys_str_mv AT chakrabartijayati sonichedgehogactsasamacrophagechemoattractantduringregenerationofthegastricepithelium
AT duaawerehmartha sonichedgehogactsasamacrophagechemoattractantduringregenerationofthegastricepithelium
AT schumachermichael sonichedgehogactsasamacrophagechemoattractantduringregenerationofthegastricepithelium
AT engevikamy sonichedgehogactsasamacrophagechemoattractantduringregenerationofthegastricepithelium
AT hawkinsjennifer sonichedgehogactsasamacrophagechemoattractantduringregenerationofthegastricepithelium
AT helmrathmichaela sonichedgehogactsasamacrophagechemoattractantduringregenerationofthegastricepithelium
AT zavrosyana sonichedgehogactsasamacrophagechemoattractantduringregenerationofthegastricepithelium