Developmental regulation of GDNF response and receptor expression in the enteric nervous system
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作者:
Worley, DS
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机构:Brandeis Univ, Dept Biol, Waltham, MA 02454 USA
Worley, DS
Pisano, JM
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机构:Brandeis Univ, Dept Biol, Waltham, MA 02454 USA
Pisano, JM
Choi, ED
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机构:Brandeis Univ, Dept Biol, Waltham, MA 02454 USA
Choi, ED
Walus, L
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机构:Brandeis Univ, Dept Biol, Waltham, MA 02454 USA
Walus, L
Hession, CA
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机构:Brandeis Univ, Dept Biol, Waltham, MA 02454 USA
Hession, CA
Cate, RL
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机构:Brandeis Univ, Dept Biol, Waltham, MA 02454 USA
Cate, RL
Sanicola, M
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机构:Brandeis Univ, Dept Biol, Waltham, MA 02454 USA
Sanicola, M
Birren, SJ
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机构:
Brandeis Univ, Dept Biol, Waltham, MA 02454 USABrandeis Univ, Dept Biol, Waltham, MA 02454 USA
Birren, SJ
[1
]
机构:
[1] Brandeis Univ, Dept Biol, Waltham, MA 02454 USA
[2] Brandeis Univ, Volen Natl Ctr Complex Syst, Waltham, MA 02454 USA
[3] Biogen Inc, Dept Mol Genet, Cambridge, MA 02142 USA
[4] Biogen Inc, Dept Prot Chem, Cambridge, MA 02142 USA
来源:
DEVELOPMENT
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2000年
/
127卷
/
20期
关键词:
GDNF;
Ret;
GFR alpha-1;
enteric nervous system;
receptor;
signaling;
rat;
D O I:
暂无
中图分类号:
Q [生物科学];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
The development of the enteric nervous system is dependent upon the actions of glial cell line-derived neurotrophic factor (GDNF) on neural crest-derived precursor cells in the embryonic gut. GDNF treatment of cultured enteric precursor cells leads to an increase in the number of neurons that develop and/or survive, sere we demonstrate that, although GDNF promoted an increase in neuron number at all embryonic ages examined, there was a developmental shift from a mitogenic to a trophic response by the developing enteric neurons. The timing of this shift corresponded to developmental changes in gut expression of GFR alpha -1, a co-receptor in the GDNF-Ret signaling complex. GFRa-1 was broadly expressed in the gut at early developmental stages, at which times soluble GFR alpha -1 was released into the medium by cultured gut cells. At later times, GFR alpha -1 became restricted to neural crest-derived cells, GFR alpha -1 could participate in GDNF signaling when expressed in cis on the surface of enteric precursor cells, or as a soluble protein, The GDNF-mediated response was greater when cell surface, compared with soluble, GFR alpha -1 was present, with the maximal response seen the presence of both cis and trans forms of GFR alpha -1, In addition to contributing to GDNF signaling, cell-surface GFR alpha -1 modulated the specificity of interactions between GDNF and soluble GFR alphas, These experiments demonstrate that complex, developmentally regulated, signaling interactions contribute to the GDNF-dependent development of enteric neurons.