E-cadherin expression in postnatal Schwann cells is regulated by the cAMP-dependent protein kinase a pathway.
E-cadherin expression in postnatal Schwann cells is regulated by the cAMP-dependent protein kinase a pathway.
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依赖CAMP依赖性蛋白激酶A途径在产后雪旺氏细胞中的E-钙粘蛋白表达受到调节。
DOI:
10.1002/glia.20716
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发表时间:
2008-11-15
期刊:
影响因子:
6.2
通讯作者:
Kim, Haesun A.
中科院分区:
文献类型:
--
作者:
Crawford, Audrita T.;Desai, Darshan;Gokina, Pradeepa;Basak, Sayantani;Kim, Haesun A.
Expression of E-cadherin in the peripheral nervous system is a highly regulated process that appears postnatally in concert with the development of myelinating Schwann cell lineage. As a major component of autotypic junctions, E-cadherin plays an important role in maintaining the structural integrity of non-compact myelin regions. In vivo, the appearance of E-cadherin in postnatal Schwann cell is accompanied by the disappearance of N-cadherin, suggesting reciprocal regulation of the two cadherins during Schwann cell development. The molecular signal that regulates the cadherin switch in Schwann cell is unclear. Using a neuron-Schwann cell co-culture system, here we show that E-cadherin expression is induced by components on the axonal membrane. We also show that the axonal effect is mediated through cAMP-dependent protein kinase A (cAMP-PKA) activation in the Schwann cell: 1) inhibition of cAMP-PKA blocks axon-induced E-cadherin expression and 2) cAMP elevation in the Schwann cell is sufficient to induce E-cadherin expression. In addition, cAMP-dependent E-cadherin expression is promoted by contact between adjacent Schwann cell membranes, suggesting its role in autotypic junction formation during myelination. Furthermore, cAMP-induced E-cadherin expression is accompanied by suppression of N-cadherin expression. Therefore, we propose that axon-dependent activation of cAMP-PKA serves as a signal that promotes cadherin switch during postnatal development of Schwann cells.
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影响因子:
16.2
作者:
Howe, CL;Valletta, JS;Mobley, WC
通讯作者:
Mobley, WC
影响因子:
21.3
作者:
Batlle, E;Sancho, E;de Herreros, AG
通讯作者:
de Herreros, AG
影响因子:
16.2
作者:
LEMKE, G;LAMAR, E;PATTERSON, J
通讯作者:
PATTERSON, J
影响因子:
7.8
作者:
Fannon, A M;Sherman, D L;Ilyina-Gragerova, G;Brophy, P J;Friedrich, V L Jr;Colman, D R
通讯作者:
Colman, D R
DOI:
10.1007/bf01188399
发表时间:
1990-06-01
期刊:
JOURNAL OF NEUROCYTOLOGY
影响因子:
--
作者:
GOULD, RM;MATTINGLY, G
通讯作者:
MATTINGLY, G