Cargando…

Insulin-like Growth Factor II: An Essential Adult Stem Cell Niche Constituent in Brain and Intestine

Tissue-specific stem cells have unique properties and growth requirements, but a small set of juxtacrine and paracrine signals have been identified that are required across multiple niches. Whereas insulin-like growth factor II (IGF-II) is necessary for prenatal growth, its role in adult stem cell p...

Descripción completa

Detalles Bibliográficos
Autores principales: Ziegler, Amber N., Feng, Qiang, Chidambaram, Shravanthi, Testai, Jaimie M., Kumari, Ekta, Rothbard, Deborah E., Constancia, Miguel, Sandovici, Ionel, Cominski, Tara, Pang, Kevin, Gao, Nan, Wood, Teresa L., Levison, Steven W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6450461/
https://www.ncbi.nlm.nih.gov/pubmed/30905741
http://dx.doi.org/10.1016/j.stemcr.2019.02.011
_version_ 1783409027144744960
author Ziegler, Amber N.
Feng, Qiang
Chidambaram, Shravanthi
Testai, Jaimie M.
Kumari, Ekta
Rothbard, Deborah E.
Constancia, Miguel
Sandovici, Ionel
Cominski, Tara
Pang, Kevin
Gao, Nan
Wood, Teresa L.
Levison, Steven W.
author_facet Ziegler, Amber N.
Feng, Qiang
Chidambaram, Shravanthi
Testai, Jaimie M.
Kumari, Ekta
Rothbard, Deborah E.
Constancia, Miguel
Sandovici, Ionel
Cominski, Tara
Pang, Kevin
Gao, Nan
Wood, Teresa L.
Levison, Steven W.
author_sort Ziegler, Amber N.
collection PubMed
description Tissue-specific stem cells have unique properties and growth requirements, but a small set of juxtacrine and paracrine signals have been identified that are required across multiple niches. Whereas insulin-like growth factor II (IGF-II) is necessary for prenatal growth, its role in adult stem cell physiology is largely unknown. We show that loss of Igf2 in adult mice resulted in a ∼50% reduction in slowly dividing, label-retaining cells in the two regions of the brain that harbor neural stem cells. Concordantly, induced Igf2 deletion increased newly generated neurons in the olfactory bulb accompanied by hyposmia, and caused impairments in learning and memory and increased anxiety. Induced Igf2 deletion also resulted in rapid loss of stem and progenitor cells in the crypts of Lieberkühn, leading to body-weight loss and lethality and the inability to produce organoids in vitro. These data demonstrate that IGF-II is critical for multiple adult stem cell niches.
format Online
Article
Text
id pubmed-6450461
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-64504612019-04-16 Insulin-like Growth Factor II: An Essential Adult Stem Cell Niche Constituent in Brain and Intestine Ziegler, Amber N. Feng, Qiang Chidambaram, Shravanthi Testai, Jaimie M. Kumari, Ekta Rothbard, Deborah E. Constancia, Miguel Sandovici, Ionel Cominski, Tara Pang, Kevin Gao, Nan Wood, Teresa L. Levison, Steven W. Stem Cell Reports Article Tissue-specific stem cells have unique properties and growth requirements, but a small set of juxtacrine and paracrine signals have been identified that are required across multiple niches. Whereas insulin-like growth factor II (IGF-II) is necessary for prenatal growth, its role in adult stem cell physiology is largely unknown. We show that loss of Igf2 in adult mice resulted in a ∼50% reduction in slowly dividing, label-retaining cells in the two regions of the brain that harbor neural stem cells. Concordantly, induced Igf2 deletion increased newly generated neurons in the olfactory bulb accompanied by hyposmia, and caused impairments in learning and memory and increased anxiety. Induced Igf2 deletion also resulted in rapid loss of stem and progenitor cells in the crypts of Lieberkühn, leading to body-weight loss and lethality and the inability to produce organoids in vitro. These data demonstrate that IGF-II is critical for multiple adult stem cell niches. Elsevier 2019-03-21 /pmc/articles/PMC6450461/ /pubmed/30905741 http://dx.doi.org/10.1016/j.stemcr.2019.02.011 Text en © 2019 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Ziegler, Amber N.
Feng, Qiang
Chidambaram, Shravanthi
Testai, Jaimie M.
Kumari, Ekta
Rothbard, Deborah E.
Constancia, Miguel
Sandovici, Ionel
Cominski, Tara
Pang, Kevin
Gao, Nan
Wood, Teresa L.
Levison, Steven W.
Insulin-like Growth Factor II: An Essential Adult Stem Cell Niche Constituent in Brain and Intestine
title Insulin-like Growth Factor II: An Essential Adult Stem Cell Niche Constituent in Brain and Intestine
title_full Insulin-like Growth Factor II: An Essential Adult Stem Cell Niche Constituent in Brain and Intestine
title_fullStr Insulin-like Growth Factor II: An Essential Adult Stem Cell Niche Constituent in Brain and Intestine
title_full_unstemmed Insulin-like Growth Factor II: An Essential Adult Stem Cell Niche Constituent in Brain and Intestine
title_short Insulin-like Growth Factor II: An Essential Adult Stem Cell Niche Constituent in Brain and Intestine
title_sort insulin-like growth factor ii: an essential adult stem cell niche constituent in brain and intestine
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6450461/
https://www.ncbi.nlm.nih.gov/pubmed/30905741
http://dx.doi.org/10.1016/j.stemcr.2019.02.011
work_keys_str_mv AT zieglerambern insulinlikegrowthfactoriianessentialadultstemcellnicheconstituentinbrainandintestine
AT fengqiang insulinlikegrowthfactoriianessentialadultstemcellnicheconstituentinbrainandintestine
AT chidambaramshravanthi insulinlikegrowthfactoriianessentialadultstemcellnicheconstituentinbrainandintestine
AT testaijaimiem insulinlikegrowthfactoriianessentialadultstemcellnicheconstituentinbrainandintestine
AT kumariekta insulinlikegrowthfactoriianessentialadultstemcellnicheconstituentinbrainandintestine
AT rothbarddeborahe insulinlikegrowthfactoriianessentialadultstemcellnicheconstituentinbrainandintestine
AT constanciamiguel insulinlikegrowthfactoriianessentialadultstemcellnicheconstituentinbrainandintestine
AT sandoviciionel insulinlikegrowthfactoriianessentialadultstemcellnicheconstituentinbrainandintestine
AT cominskitara insulinlikegrowthfactoriianessentialadultstemcellnicheconstituentinbrainandintestine
AT pangkevin insulinlikegrowthfactoriianessentialadultstemcellnicheconstituentinbrainandintestine
AT gaonan insulinlikegrowthfactoriianessentialadultstemcellnicheconstituentinbrainandintestine
AT woodteresal insulinlikegrowthfactoriianessentialadultstemcellnicheconstituentinbrainandintestine
AT levisonstevenw insulinlikegrowthfactoriianessentialadultstemcellnicheconstituentinbrainandintestine