c-Myb is required for progenitor cell homeostasis in colonic crypts

J. Malaterre; M. Carpinelli; M. Ernst; W. Alexander; M. Cooke; S. Sutton; S. Dworkin; J.K. Heakth; J. Frampton; G. McArthur; J.C. Clevers; D. Hilton; Th. Mantamadiotis; R.G. Ramsay

c-Myb is required for progenitor cell homeostasis in colonic crypts

J. Malaterre, M. Carpinelli, M. Ernst, W. Alexander, M. Cooke, S. Sutton, S. Dworkin, J.K. Heakth, J. Frampton, G. McArthur, J.C. Clevers, D. Hilton, Th. Mantamadiotis, R.G. Ramsay

Hubrecht Institute

Onderzoeksoutput: Bijdrage aan wetenschappelijk tijdschrift/periodieke uitgave › Artikel › Wetenschappelijk › peer review

93 Citaten (Scopus)

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The colonic crypt is the functional unit of the colon mucosa with a central role in ion and water reabsorption. Under steady-state conditions, the distal colonic crypt harbors a single stem cell at its base that gives rise to highly proliferative progenitor cells that differentiate into columnar, goblet, and endocrine cells. The role of c-Myb in crypt homeostasis has not been elucidated. Here we have studied three genetically distinct hypomorphic c-myb mutant mouse strains, all of which show reduced colonic crypt size. The mutations target the key domains of the transcription factor: the DNA binding, transactivation, and negative regulatory domains. In vivo proliferation and cell cycle marker studies suggest that these mice have a progenitor cell proliferation defect mediated in part by reduced Cyclin E1 expression. To independently assess the extent to which c-myb is required for colonic crypt homeostasis we also generated a novel tissue-specific mouse model to allow the deletion of c-myb in adult colon, and using these mice we show that c-Myb is required for crypt integrity, normal differentiation, and steady-state proliferation.

Originele taal-2	Engels
Pagina's (van-tot)	3829-3834
Tijdschrift	Proceedings of the National Academy of Sciences of the United States of America
Volume	104
Status	Gepubliceerd - 2007

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Malaterre, J., Carpinelli, M., Ernst, M., Alexander, W., Cooke, M., Sutton, S., Dworkin, S., Heakth, J. K., Frampton, J., McArthur, G., Clevers, J. C., Hilton, D., Mantamadiotis, T., & Ramsay, R. G. (2007). c-Myb is required for progenitor cell homeostasis in colonic crypts. Proceedings of the National Academy of Sciences of the United States of America, 104, 3829-3834.

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title = "c-Myb is required for progenitor cell homeostasis in colonic crypts",

abstract = "The colonic crypt is the functional unit of the colon mucosa with a central role in ion and water reabsorption. Under steady-state conditions, the distal colonic crypt harbors a single stem cell at its base that gives rise to highly proliferative progenitor cells that differentiate into columnar, goblet, and endocrine cells. The role of c-Myb in crypt homeostasis has not been elucidated. Here we have studied three genetically distinct hypomorphic c-myb mutant mouse strains, all of which show reduced colonic crypt size. The mutations target the key domains of the transcription factor: the DNA binding, transactivation, and negative regulatory domains. In vivo proliferation and cell cycle marker studies suggest that these mice have a progenitor cell proliferation defect mediated in part by reduced Cyclin E1 expression. To independently assess the extent to which c-myb is required for colonic crypt homeostasis we also generated a novel tissue-specific mouse model to allow the deletion of c-myb in adult colon, and using these mice we show that c-Myb is required for crypt integrity, normal differentiation, and steady-state proliferation.",

author = "J. Malaterre and M. Carpinelli and M. Ernst and W. Alexander and M. Cooke and S. Sutton and S. Dworkin and J.K. Heakth and J. Frampton and G. McArthur and J.C. Clevers and D. Hilton and Th. Mantamadiotis and R.G. Ramsay",

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T1 - c-Myb is required for progenitor cell homeostasis in colonic crypts

AU - Malaterre, J.

AU - Carpinelli, M.

AU - Ernst, M.

AU - Alexander, W.

AU - Cooke, M.

AU - Sutton, S.

AU - Dworkin, S.

AU - Heakth, J.K.

AU - Frampton, J.

AU - McArthur, G.

AU - Clevers, J.C.

AU - Hilton, D.

AU - Mantamadiotis, Th.

AU - Ramsay, R.G.

N1 - doi: 10.1073/pnas.0610055104. PMC_URL: http://www.pubmedcentral.nih.gov/picrender.fcgi?tool=pmcentrez&artid=1820669&blobtype=pdf

PY - 2007

Y1 - 2007

N2 - The colonic crypt is the functional unit of the colon mucosa with a central role in ion and water reabsorption. Under steady-state conditions, the distal colonic crypt harbors a single stem cell at its base that gives rise to highly proliferative progenitor cells that differentiate into columnar, goblet, and endocrine cells. The role of c-Myb in crypt homeostasis has not been elucidated. Here we have studied three genetically distinct hypomorphic c-myb mutant mouse strains, all of which show reduced colonic crypt size. The mutations target the key domains of the transcription factor: the DNA binding, transactivation, and negative regulatory domains. In vivo proliferation and cell cycle marker studies suggest that these mice have a progenitor cell proliferation defect mediated in part by reduced Cyclin E1 expression. To independently assess the extent to which c-myb is required for colonic crypt homeostasis we also generated a novel tissue-specific mouse model to allow the deletion of c-myb in adult colon, and using these mice we show that c-Myb is required for crypt integrity, normal differentiation, and steady-state proliferation.

AB - The colonic crypt is the functional unit of the colon mucosa with a central role in ion and water reabsorption. Under steady-state conditions, the distal colonic crypt harbors a single stem cell at its base that gives rise to highly proliferative progenitor cells that differentiate into columnar, goblet, and endocrine cells. The role of c-Myb in crypt homeostasis has not been elucidated. Here we have studied three genetically distinct hypomorphic c-myb mutant mouse strains, all of which show reduced colonic crypt size. The mutations target the key domains of the transcription factor: the DNA binding, transactivation, and negative regulatory domains. In vivo proliferation and cell cycle marker studies suggest that these mice have a progenitor cell proliferation defect mediated in part by reduced Cyclin E1 expression. To independently assess the extent to which c-myb is required for colonic crypt homeostasis we also generated a novel tissue-specific mouse model to allow the deletion of c-myb in adult colon, and using these mice we show that c-Myb is required for crypt integrity, normal differentiation, and steady-state proliferation.

M3 - Article

SN - 0027-8424

VL - 104

SP - 3829

EP - 3834

JO - Proceedings of the National Academy of Sciences of the United States of America

JF - Proceedings of the National Academy of Sciences of the United States of America

ER -

c-Myb is required for progenitor cell homeostasis in colonic crypts

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