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The role of p38b MAPK in age-related modulation of intestinal stem cell proliferation and differentiation in Drosophila.

作者信息

Park Joung-Sun, Kim Young-Shin, Yoo Mi-Ae

机构信息

Department of Molecular Biology, Pusan National University, Busan 609-735, Korea.

出版信息

Aging (Albany NY). 2009 May 21;1(7):637-51. doi: 10.18632/aging.100054.


DOI:10.18632/aging.100054
PMID:20157545
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2806044/
Abstract

It is important to understand how age-related changes in intestinal stem cells (ISCs) may contribute to age-associated intestinal diseases, including cancer. Drosophila midgut is an excellent model system for the study of ISC proliferation and differentiation. Recently, age-related changes in the Drosophila midgut have been shown to include an increase in ISC proliferation and accumulation of mis-differentiated ISC daughter cells. Here, we show that the p38b MAPK pathway contributes to the age-related changes in ISC and progenitor cells in Drosophila. D-p38b MAPK is required for an age-related increase of ISC proliferation. In addition, this pathway is involved in age and oxidative stress-associated mis-differentiation of enterocytes and upregulation of Delta, a Notch receptor ligand. Furthermore, we also show that D-p38b acts downstream of PVF2/PVR signaling in these age-related changes. Taken together, our findings suggest that p38 MAPK plays a crucial role in the balance between ISC proliferation and proper differentiation in the adult Drosophila midgut.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c1f/2806044/b418c5ed4407/aging-01-637-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c1f/2806044/2993cbd5b431/aging-01-637-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c1f/2806044/042e8c5bacfc/aging-01-637-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c1f/2806044/93690f422826/aging-01-637-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c1f/2806044/e47a3c087383/aging-01-637-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c1f/2806044/477afd863701/aging-01-637-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c1f/2806044/b418c5ed4407/aging-01-637-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c1f/2806044/2993cbd5b431/aging-01-637-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c1f/2806044/042e8c5bacfc/aging-01-637-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c1f/2806044/93690f422826/aging-01-637-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c1f/2806044/e47a3c087383/aging-01-637-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c1f/2806044/477afd863701/aging-01-637-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c1f/2806044/b418c5ed4407/aging-01-637-g006.jpg

相似文献

[1]
The role of p38b MAPK in age-related modulation of intestinal stem cell proliferation and differentiation in Drosophila.

Aging (Albany NY). 2009-5-21

[2]
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[3]
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[4]
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[5]
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[6]
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[7]
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[8]
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[9]
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[10]
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Cell Res. 2013-7-30

引用本文的文献

[1]
Measuring Anti-aging Effects in .

Bio Protoc. 2025-5-5

[2]
Dapagliflozin ameliorates intestinal stem cell aging by regulating the MAPK signaling pathway in .

Front Cell Dev Biol. 2025-4-23

[3]
The anti-aging effect of vitamin D and vitamin D receptor in midgut.

Aging (Albany NY). 2024-2-7

[4]
The septate junction component bark beetle is required for intestinal barrier function and homeostasis.

iScience. 2023-5-19

[5]
The Calcineurin-Drp1-Mediated Mitochondrial Fragmentation Is Aligned with the Differentiation of c-Kit Cardiac Progenitor Cells.

Int J Stem Cells. 2023-5-30

[6]
Aging-related upregulation of the homeobox gene caudal represses intestinal stem cell differentiation in Drosophila.

PLoS Genet. 2021-7

[7]
Neuroglian regulates Drosophila intestinal stem cell proliferation through enhanced signaling via the epidermal growth factor receptor.

Stem Cell Reports. 2021-6-8

[8]
The Act of Controlling Adult Stem Cell Dynamics: Insights from Animal Models.

Biomolecules. 2021-4-30

[9]
"Empowering" Cardiac Cells via Stem Cell Derived Mitochondrial Transplantation- Does Age Matter?

Int J Mol Sci. 2021-2-12

[10]
A glucose-supplemented diet enhances gut barrier integrity in .

Biol Open. 2021-3-8

本文引用的文献

[1]
Drosophila intestinal response to bacterial infection: activation of host defense and stem cell proliferation.

Cell Host Microbe. 2009-2-19

[2]
Intestinal stem cells in mammals and Drosophila.

Cell Stem Cell. 2009-2-6

[3]
EGFR signaling regulates the proliferation of Drosophila adult midgut progenitors.

Development. 2009-2

[4]
Tissue damage-induced intestinal stem cell division in Drosophila.

Cell Stem Cell. 2009-1-9

[5]
E-cadherin prolongs the moment for interaction between intestinal stem cell and its progenitor cell to ensure Notch signaling in adult Drosophila midgut.

Genes Cells. 2008-12

[6]
JNK activity in somatic stem cells causes loss of tissue homeostasis in the aging Drosophila gut.

Cell Stem Cell. 2008-10-9

[7]
Paracrine Wingless signalling controls self-renewal of Drosophila intestinal stem cells.

Nature. 2008-10-23

[8]
Age-related changes in Drosophila midgut are associated with PVF2, a PDGF/VEGF-like growth factor.

Aging Cell. 2008-6

[9]
Epidermal growth factor receptor signaling modulates apoptosis via p38alpha MAPK-dependent activation of Bax in intestinal epithelial cells.

Am J Physiol Gastrointest Liver Physiol. 2007-9

[10]
Multipotent Drosophila intestinal stem cells specify daughter cell fates by differential notch signaling.

Science. 2007-2-16

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