Role of Ldb1 in Adult Intestinal Homeostasis

<p>Ldb1 is an essential co-regulator of transcription in embryonic development. It acts in conjunction with nuclear LIM-homeodomain and LIM-only proteins to control key events of organogenesis as precursor cells enter lineage specification. Here we ask whether Ldb1 exerts control over stem cel...

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Main Author: Ipsita Dey-Guha, Mahua Mukhopadhyay, Matthew Phillips, Heiner Westphal
Format: Article
Language:English
Published: Ivyspring International Publisher 2009-01-01
Series:International Journal of Biological Sciences
Online Access:http://www.biolsci.org/v05p0686.htm
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spelling doaj-e0f4ae9f3b75467792d1704e2d137fc72020-11-24T22:06:50ZengIvyspring International PublisherInternational Journal of Biological Sciences1449-22882009-01-0157686694Role of Ldb1 in Adult Intestinal HomeostasisIpsita Dey-Guha, Mahua Mukhopadhyay, Matthew Phillips, Heiner Westphal<p>Ldb1 is an essential co-regulator of transcription in embryonic development. It acts in conjunction with nuclear LIM-homeodomain and LIM-only proteins to control key events of organogenesis as precursor cells enter lineage specification. Here we ask whether Ldb1 exerts control over stem cell activation and differentiation throughout the life of the organism as required for tissue homeostasis. To help answer this question, we have generated conditional <i>Ldb1</i> mouse mutants with an <i>Ldb1 floxed/floxed;ROSA26CreER </i>genotype. Tamoxifen treatment of 60 day-old mutant animals results in near-ubiquitous Cre-mediated <i>Ldb1</i> inactivation. As a consequence, the stem cell microenvironment of intestinal crypts is drastically affected. Cells that normally express Ldb1 together with markers that identify them as lineage progenitors cease to retain bromodeoxyuridine and are gradually lost. <i>Ldb1</i> inactivation in intestinal crypts and/or in neighboring mesenchymal cells also triggers activation of Wnt signaling in the stem cell niches of the small intestine. Cell proliferation is markedly increased in the epithelia of the small intestine, and <i>Lgr5-</i>expressing stem cells disappear from the base of the crypts. This perturbation of the normal process of tissue homeostasis causes apoptosis, and the animals do not survive. We conclude that Ldb1-mediated transcriptional regulation plays a major role in adult intestinal homeostasis.</p>http://www.biolsci.org/v05p0686.htm
collection DOAJ
language English
format Article
sources DOAJ
author Ipsita Dey-Guha, Mahua Mukhopadhyay, Matthew Phillips, Heiner Westphal
spellingShingle Ipsita Dey-Guha, Mahua Mukhopadhyay, Matthew Phillips, Heiner Westphal
Role of Ldb1 in Adult Intestinal Homeostasis
International Journal of Biological Sciences
author_facet Ipsita Dey-Guha, Mahua Mukhopadhyay, Matthew Phillips, Heiner Westphal
author_sort Ipsita Dey-Guha, Mahua Mukhopadhyay, Matthew Phillips, Heiner Westphal
title Role of Ldb1 in Adult Intestinal Homeostasis
title_short Role of Ldb1 in Adult Intestinal Homeostasis
title_full Role of Ldb1 in Adult Intestinal Homeostasis
title_fullStr Role of Ldb1 in Adult Intestinal Homeostasis
title_full_unstemmed Role of Ldb1 in Adult Intestinal Homeostasis
title_sort role of ldb1 in adult intestinal homeostasis
publisher Ivyspring International Publisher
series International Journal of Biological Sciences
issn 1449-2288
publishDate 2009-01-01
description <p>Ldb1 is an essential co-regulator of transcription in embryonic development. It acts in conjunction with nuclear LIM-homeodomain and LIM-only proteins to control key events of organogenesis as precursor cells enter lineage specification. Here we ask whether Ldb1 exerts control over stem cell activation and differentiation throughout the life of the organism as required for tissue homeostasis. To help answer this question, we have generated conditional <i>Ldb1</i> mouse mutants with an <i>Ldb1 floxed/floxed;ROSA26CreER </i>genotype. Tamoxifen treatment of 60 day-old mutant animals results in near-ubiquitous Cre-mediated <i>Ldb1</i> inactivation. As a consequence, the stem cell microenvironment of intestinal crypts is drastically affected. Cells that normally express Ldb1 together with markers that identify them as lineage progenitors cease to retain bromodeoxyuridine and are gradually lost. <i>Ldb1</i> inactivation in intestinal crypts and/or in neighboring mesenchymal cells also triggers activation of Wnt signaling in the stem cell niches of the small intestine. Cell proliferation is markedly increased in the epithelia of the small intestine, and <i>Lgr5-</i>expressing stem cells disappear from the base of the crypts. This perturbation of the normal process of tissue homeostasis causes apoptosis, and the animals do not survive. We conclude that Ldb1-mediated transcriptional regulation plays a major role in adult intestinal homeostasis.</p>
url http://www.biolsci.org/v05p0686.htm
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