Cell adhesion molecule L1 affects the rate of differentiation of enteric neurons in the developing gut.

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Cell adhesion molecule L1 affects the rate of differentiation of enteric neurons in the developing gut. / Turner, Kirsty N; Schachner, Melitta; Anderson, Richard B.

in: DEV DYNAM, Jahrgang 238, Nr. 3, 3, 2009, S. 708-715.

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@article{19255c44a8de45849a0426909a3566c3,
title = "Cell adhesion molecule L1 affects the rate of differentiation of enteric neurons in the developing gut.",
abstract = "The enteric nervous system arises predominantly from vagal level neural crest cells that migrate into and along the developing gut. As the neural crest-derived cells migrate within the gut, a subpopulation begins to differentiate into enteric neurons. Here, we show that the differentiation of neural crest-derived cells into enteric neurons is delayed in L1-deficient mice, compared with littermate controls. However, glial cell differentiation is not affected in L1-deficient mice. These mice also show a delay in the differentiation of a neurotransmitter-specific subtype of enteric neuron within the gastrointestinal tract. Together, these results suggest a role for the cell adhesion molecule, L1, in the differentiation of neural crest-derived cells into enteric neurons within the developing enteric nervous system.",
author = "Turner, {Kirsty N} and Melitta Schachner and Anderson, {Richard B}",
year = "2009",
language = "Deutsch",
volume = "238",
pages = "708--715",
journal = "DEV DYNAM",
issn = "1058-8388",
publisher = "Wiley-Liss Inc.",
number = "3",

}

RIS

TY - JOUR

T1 - Cell adhesion molecule L1 affects the rate of differentiation of enteric neurons in the developing gut.

AU - Turner, Kirsty N

AU - Schachner, Melitta

AU - Anderson, Richard B

PY - 2009

Y1 - 2009

N2 - The enteric nervous system arises predominantly from vagal level neural crest cells that migrate into and along the developing gut. As the neural crest-derived cells migrate within the gut, a subpopulation begins to differentiate into enteric neurons. Here, we show that the differentiation of neural crest-derived cells into enteric neurons is delayed in L1-deficient mice, compared with littermate controls. However, glial cell differentiation is not affected in L1-deficient mice. These mice also show a delay in the differentiation of a neurotransmitter-specific subtype of enteric neuron within the gastrointestinal tract. Together, these results suggest a role for the cell adhesion molecule, L1, in the differentiation of neural crest-derived cells into enteric neurons within the developing enteric nervous system.

AB - The enteric nervous system arises predominantly from vagal level neural crest cells that migrate into and along the developing gut. As the neural crest-derived cells migrate within the gut, a subpopulation begins to differentiate into enteric neurons. Here, we show that the differentiation of neural crest-derived cells into enteric neurons is delayed in L1-deficient mice, compared with littermate controls. However, glial cell differentiation is not affected in L1-deficient mice. These mice also show a delay in the differentiation of a neurotransmitter-specific subtype of enteric neuron within the gastrointestinal tract. Together, these results suggest a role for the cell adhesion molecule, L1, in the differentiation of neural crest-derived cells into enteric neurons within the developing enteric nervous system.

M3 - SCORING: Zeitschriftenaufsatz

VL - 238

SP - 708

EP - 715

JO - DEV DYNAM

JF - DEV DYNAM

SN - 1058-8388

IS - 3

M1 - 3

ER -