Lack of beta 1 integrins in enteric neural crest cells leads to a Hirschsprung-like phenotype

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Breau, M., Pietri, T., Eder, O., Blanche, M., Brakebusch, C., Fassler, R., Thiery, J., & Dufour, S. (2006). Lack of beta 1 integrins in enteric neural crest cells leads to a Hirschsprung-like phenotype. Development, 133(9). https://doi.org/10.1242/dev.02346

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@article{Breau2006_258,
  author = {Breau, MA and Pietri, T and Eder, O and Blanche, M and Brakebusch, C and Fassler, R and Thiery, JP and Dufour, S},
  year = {2006},
  month = {5},
  title = {Lack of beta 1 integrins in enteric neural crest cells leads to a Hirschsprung-like phenotype},
  journal = {Development},
  publisher = {COMPANY OF BIOLOGISTS LTD},
  volume = {133},
  number = {9},
  address = {BIDDER BUILDING CAMBRIDGE COMMERCIAL PARK COWLEY RD, CAMBRIDGE CB4 4DL,   CAMBS, ENGLAND},
  abstract = {The enteric nervous system arises mainly from vagal and sacral neural crest cells that colonise the gut between 9.5 and 14 days of development in mice. Using the Cre-LoxP system, we removed beta 1 integrins in the neural crest cells when they emerge from the neural tube. beta 1-null enteric neural crest cells fail to colonise the gut completely, leading to an aganglionosis of the descending colon, which resembles the human Hirschsprung's disease. Moreover, beta 1-null enteric neural crest cells form abnormal aggregates in the gut wall, leading to a severe alteration of the ganglia network organisation. Organotypic cultures of gut explants reveal that beta 1-null enteric neural crest cells show impaired adhesion on extracellular matrix and enhanced intercellular adhesion properties. They display migration defects in collagen gels and gut tissue environments. We also provide evidence that beta 1 integrins are required for the villi innervation in the small intestine. Our findings highlight the crucial roles played by beta 1 integrins at various steps of enteric nervous system development.},
  url = {http://www.dx.doi.org/10.1242/dev.02346},
  doi = {10.1242/dev.02346},
  issn = {0950-1991},
}

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TY  - JOUR
AU  - Breau, MA
AU  - Pietri, T
AU  - Eder, O
AU  - Blanche, M
AU  - Brakebusch, C
AU  - Fassler, R
AU  - Thiery, JP
AU  - Dufour, S
PY  - 2006
DA  - 2006/05/01
TI  - Lack of beta 1 integrins in enteric neural crest cells leads to a Hirschsprung-like phenotype
JO  - Development
VL  - 133
IS  - 9
PB  - COMPANY OF BIOLOGISTS LTD
SN  - 0950-1991
AB  - The enteric nervous system arises mainly from vagal and sacral neural crest cells that colonise the gut between 9.5 and 14 days of development in mice. Using the Cre-LoxP system, we removed beta 1 integrins in the neural crest cells when they emerge from the neural tube. beta 1-null enteric neural crest cells fail to colonise the gut completely, leading to an aganglionosis of the descending colon, which resembles the human Hirschsprung's disease. Moreover, beta 1-null enteric neural crest cells form abnormal aggregates in the gut wall, leading to a severe alteration of the ganglia network organisation. Organotypic cultures of gut explants reveal that beta 1-null enteric neural crest cells show impaired adhesion on extracellular matrix and enhanced intercellular adhesion properties. They display migration defects in collagen gels and gut tissue environments. We also provide evidence that beta 1 integrins are required for the villi innervation in the small intestine. Our findings highlight the crucial roles played by beta 1 integrins at various steps of enteric nervous system development.
DO  - 10.1242/dev.02346
UR  - http://www.dx.doi.org/10.1242/dev.02346
ER  -