Zymosan-A promotes the regeneration of intestinal stem cells by upregulating ASCL2

Abstract Intestinal stem cells (ISCs) are responsible for intestinal tissue homeostasis and are important for the regeneration of the damaged intestinal epithelia. Through the establishment of ionizing radiation (IR) induced intestinal injury model, we found that a TLR2 agonist, Zymosan-A, promoted...

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Main Authors: Jicong Du, Lan Fang, Jianpeng Zhao, Yike Yu, Zhenlan Feng, Yuedong Wang, Ying Cheng, Bailong Li, Fu Gao, Cong Liu
Format: Article
Language:English
Published: Nature Publishing Group 2022-10-01
Series:Cell Death and Disease
Online Access:https://doi.org/10.1038/s41419-022-05301-x
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author Jicong Du
Lan Fang
Jianpeng Zhao
Yike Yu
Zhenlan Feng
Yuedong Wang
Ying Cheng
Bailong Li
Fu Gao
Cong Liu
author_facet Jicong Du
Lan Fang
Jianpeng Zhao
Yike Yu
Zhenlan Feng
Yuedong Wang
Ying Cheng
Bailong Li
Fu Gao
Cong Liu
author_sort Jicong Du
collection DOAJ
description Abstract Intestinal stem cells (ISCs) are responsible for intestinal tissue homeostasis and are important for the regeneration of the damaged intestinal epithelia. Through the establishment of ionizing radiation (IR) induced intestinal injury model, we found that a TLR2 agonist, Zymosan-A, promoted the regeneration of ISCs in vivo and in vitro. Zymosan-A improved the survival of abdominal irradiated mice (81.82% of mice in the treated group vs. 30% of mice in the PBS group), inhibited the radiation damage of intestinal tissue, increased the survival rate of intestinal crypts and the number of ISCs after lethal IR in vivo. Through organoid experiments, we found that Zymosan-A promoted the proliferation and differentiation of ISCs after IR. Remarkably, the results of RNA sequencing and Western Blot (WB) showed that Zymosan-A reduced IR-induced intestinal injury via TLR2 signaling pathway and Wnt signaling pathway and Zymosan-A had no radioprotection on TLR2 KO mice, suggesting that Zymosan-A may play a radioprotective role by targeting TLR2. Moreover, our results revealed that Zymosan-A increased ASCL2, a transcription factor of ISCs, playing a core role in the process of Zymosan-A against IR-induced intestinal injury and likely contributing to the survival of intestinal organoids post-radiation. In conclusion, we demonstrated that Zymosan-A promotes the regeneration of ISCs by upregulating ASCL2.
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spelling doaj.art-2c6f489c5c774627840baadca7c6eac02022-12-22T04:07:22ZengNature Publishing GroupCell Death and Disease2041-48892022-10-01131011110.1038/s41419-022-05301-xZymosan-A promotes the regeneration of intestinal stem cells by upregulating ASCL2Jicong Du0Lan Fang1Jianpeng Zhao2Yike Yu3Zhenlan Feng4Yuedong Wang5Ying Cheng6Bailong Li7Fu Gao8Cong Liu9Department of Radiation Medicine, Faculty of Naval Medicine, Naval Medical UniversityDepartment of Radiation Medicine, Faculty of Naval Medicine, Naval Medical UniversityDepartment of Radiation Medicine, Faculty of Naval Medicine, Naval Medical UniversityDepartment of Radiation Medicine, Faculty of Naval Medicine, Naval Medical UniversityDepartment of Radiation Medicine, Faculty of Naval Medicine, Naval Medical UniversityDepartment of Radiation Medicine, Faculty of Naval Medicine, Naval Medical UniversityDepartment of Radiation Medicine, Faculty of Naval Medicine, Naval Medical UniversityDepartment of Radiation Medicine, Faculty of Naval Medicine, Naval Medical UniversityDepartment of Radiation Medicine, Faculty of Naval Medicine, Naval Medical UniversityDepartment of Radiation Medicine, Faculty of Naval Medicine, Naval Medical UniversityAbstract Intestinal stem cells (ISCs) are responsible for intestinal tissue homeostasis and are important for the regeneration of the damaged intestinal epithelia. Through the establishment of ionizing radiation (IR) induced intestinal injury model, we found that a TLR2 agonist, Zymosan-A, promoted the regeneration of ISCs in vivo and in vitro. Zymosan-A improved the survival of abdominal irradiated mice (81.82% of mice in the treated group vs. 30% of mice in the PBS group), inhibited the radiation damage of intestinal tissue, increased the survival rate of intestinal crypts and the number of ISCs after lethal IR in vivo. Through organoid experiments, we found that Zymosan-A promoted the proliferation and differentiation of ISCs after IR. Remarkably, the results of RNA sequencing and Western Blot (WB) showed that Zymosan-A reduced IR-induced intestinal injury via TLR2 signaling pathway and Wnt signaling pathway and Zymosan-A had no radioprotection on TLR2 KO mice, suggesting that Zymosan-A may play a radioprotective role by targeting TLR2. Moreover, our results revealed that Zymosan-A increased ASCL2, a transcription factor of ISCs, playing a core role in the process of Zymosan-A against IR-induced intestinal injury and likely contributing to the survival of intestinal organoids post-radiation. In conclusion, we demonstrated that Zymosan-A promotes the regeneration of ISCs by upregulating ASCL2.https://doi.org/10.1038/s41419-022-05301-x
spellingShingle Jicong Du
Lan Fang
Jianpeng Zhao
Yike Yu
Zhenlan Feng
Yuedong Wang
Ying Cheng
Bailong Li
Fu Gao
Cong Liu
Zymosan-A promotes the regeneration of intestinal stem cells by upregulating ASCL2
Cell Death and Disease
title Zymosan-A promotes the regeneration of intestinal stem cells by upregulating ASCL2
title_full Zymosan-A promotes the regeneration of intestinal stem cells by upregulating ASCL2
title_fullStr Zymosan-A promotes the regeneration of intestinal stem cells by upregulating ASCL2
title_full_unstemmed Zymosan-A promotes the regeneration of intestinal stem cells by upregulating ASCL2
title_short Zymosan-A promotes the regeneration of intestinal stem cells by upregulating ASCL2
title_sort zymosan a promotes the regeneration of intestinal stem cells by upregulating ascl2
url https://doi.org/10.1038/s41419-022-05301-x
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