Canonical Wnt Signaling Ameliorates Aging of Intestinal Stem Cells

Although intestinal homeostasis is maintained by intestinal stem cells (ISCs), regeneration is impaired upon aging. Here, we first uncover changes in intestinal architecture, cell number, and cell composition upon aging. Second, we identify a decline in the regenerative capacity of ISCs upon aging b...

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Main Authors: Kodandaramireddy Nalapareddy, Kalpana J. Nattamai, Rupali S. Kumar, Rebekah Karns, Kathryn A. Wikenheiser-Brokamp, Leesa L. Sampson, Maxime M. Mahe, Nambirajan Sundaram, Mary-Beth Yacyshyn, Bruce Yacyshyn, Michael A. Helmrath, Yi Zheng, Hartmut Geiger
Format: Article
Language:English
Published: Elsevier 2017-03-01
Series:Cell Reports
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2211124717302541
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spelling doaj-c6980a428dc64392a7a39bc4956b9d032020-11-25T01:07:24ZengElsevierCell Reports2211-12472017-03-0118112608262110.1016/j.celrep.2017.02.056Canonical Wnt Signaling Ameliorates Aging of Intestinal Stem CellsKodandaramireddy Nalapareddy0Kalpana J. Nattamai1Rupali S. Kumar2Rebekah Karns3Kathryn A. Wikenheiser-Brokamp4Leesa L. Sampson5Maxime M. Mahe6Nambirajan Sundaram7Mary-Beth Yacyshyn8Bruce Yacyshyn9Michael A. Helmrath10Yi Zheng11Hartmut Geiger12Division of Experimental Hematology and Cancer Biology, Cincinnati Children’s Hospital Medical Center and University of Cincinnati, Cincinnati, OH 45229, USADivision of Experimental Hematology and Cancer Biology, Cincinnati Children’s Hospital Medical Center and University of Cincinnati, Cincinnati, OH 45229, USADivision of Experimental Hematology and Cancer Biology, Cincinnati Children’s Hospital Medical Center and University of Cincinnati, Cincinnati, OH 45229, USADivision of Gastroenterology, Hepatology, and Nutrition, Cincinnati Children’s Hospital Medical Center and University of Cincinnati, Cincinnati, OH 45229, USADivisions of Pathology and Laboratory Medicine and Pulmonary Biology, Perinatal Institute, Cincinnati Children’s Hospital Medical Center and Department of Pathology and Laboratory Medicine, University of Cincinnati, Cincinnati, OH 45229, USADivision of Experimental Hematology and Cancer Biology, Cincinnati Children’s Hospital Medical Center and University of Cincinnati, Cincinnati, OH 45229, USADivision of Pediatric General and Thoracic Surgery, Cincinnati Children’s Hospital Medical Center and University of Cincinnati, Cincinnati, OH 45229, USADivision of Pediatric General and Thoracic Surgery, Cincinnati Children’s Hospital Medical Center and University of Cincinnati, Cincinnati, OH 45229, USADivision of Digestive Diseases, University of Cincinnati, Cincinnati, OH 45229, USADivision of Digestive Diseases, University of Cincinnati, Cincinnati, OH 45229, USADivision of Pediatric General and Thoracic Surgery, Cincinnati Children’s Hospital Medical Center and University of Cincinnati, Cincinnati, OH 45229, USADivision of Experimental Hematology and Cancer Biology, Cincinnati Children’s Hospital Medical Center and University of Cincinnati, Cincinnati, OH 45229, USADivision of Experimental Hematology and Cancer Biology, Cincinnati Children’s Hospital Medical Center and University of Cincinnati, Cincinnati, OH 45229, USAAlthough intestinal homeostasis is maintained by intestinal stem cells (ISCs), regeneration is impaired upon aging. Here, we first uncover changes in intestinal architecture, cell number, and cell composition upon aging. Second, we identify a decline in the regenerative capacity of ISCs upon aging because of a decline in canonical Wnt signaling in ISCs. Changes in expression of Wnts are found in stem cells themselves and in their niche, including Paneth cells and mesenchyme. Third, reactivating canonical Wnt signaling enhances the function of both murine and human ISCs and, thus, ameliorates aging-associated phenotypes of ISCs in an organoid assay. Our data demonstrate a role for impaired Wnt signaling in physiological aging of ISCs and further identify potential therapeutic avenues to improve ISC regenerative potential upon aging.http://www.sciencedirect.com/science/article/pii/S2211124717302541agingregenerationintestinal stem cellsWnt signaling
collection DOAJ
language English
format Article
sources DOAJ
author Kodandaramireddy Nalapareddy
Kalpana J. Nattamai
Rupali S. Kumar
Rebekah Karns
Kathryn A. Wikenheiser-Brokamp
Leesa L. Sampson
Maxime M. Mahe
Nambirajan Sundaram
Mary-Beth Yacyshyn
Bruce Yacyshyn
Michael A. Helmrath
Yi Zheng
Hartmut Geiger
spellingShingle Kodandaramireddy Nalapareddy
Kalpana J. Nattamai
Rupali S. Kumar
Rebekah Karns
Kathryn A. Wikenheiser-Brokamp
Leesa L. Sampson
Maxime M. Mahe
Nambirajan Sundaram
Mary-Beth Yacyshyn
Bruce Yacyshyn
Michael A. Helmrath
Yi Zheng
Hartmut Geiger
Canonical Wnt Signaling Ameliorates Aging of Intestinal Stem Cells
Cell Reports
aging
regeneration
intestinal stem cells
Wnt signaling
author_facet Kodandaramireddy Nalapareddy
Kalpana J. Nattamai
Rupali S. Kumar
Rebekah Karns
Kathryn A. Wikenheiser-Brokamp
Leesa L. Sampson
Maxime M. Mahe
Nambirajan Sundaram
Mary-Beth Yacyshyn
Bruce Yacyshyn
Michael A. Helmrath
Yi Zheng
Hartmut Geiger
author_sort Kodandaramireddy Nalapareddy
title Canonical Wnt Signaling Ameliorates Aging of Intestinal Stem Cells
title_short Canonical Wnt Signaling Ameliorates Aging of Intestinal Stem Cells
title_full Canonical Wnt Signaling Ameliorates Aging of Intestinal Stem Cells
title_fullStr Canonical Wnt Signaling Ameliorates Aging of Intestinal Stem Cells
title_full_unstemmed Canonical Wnt Signaling Ameliorates Aging of Intestinal Stem Cells
title_sort canonical wnt signaling ameliorates aging of intestinal stem cells
publisher Elsevier
series Cell Reports
issn 2211-1247
publishDate 2017-03-01
description Although intestinal homeostasis is maintained by intestinal stem cells (ISCs), regeneration is impaired upon aging. Here, we first uncover changes in intestinal architecture, cell number, and cell composition upon aging. Second, we identify a decline in the regenerative capacity of ISCs upon aging because of a decline in canonical Wnt signaling in ISCs. Changes in expression of Wnts are found in stem cells themselves and in their niche, including Paneth cells and mesenchyme. Third, reactivating canonical Wnt signaling enhances the function of both murine and human ISCs and, thus, ameliorates aging-associated phenotypes of ISCs in an organoid assay. Our data demonstrate a role for impaired Wnt signaling in physiological aging of ISCs and further identify potential therapeutic avenues to improve ISC regenerative potential upon aging.
topic aging
regeneration
intestinal stem cells
Wnt signaling
url http://www.sciencedirect.com/science/article/pii/S2211124717302541
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