首页> 外文期刊>Developmental biology >Age-dependent differences in the effects of GDNF and NT-3 on the development of neurons and glia from neural crest-derived precursors immunoselected from the fetal rat gut: Expression of GFR alpha-1 in vitro and in vivo
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Age-dependent differences in the effects of GDNF and NT-3 on the development of neurons and glia from neural crest-derived precursors immunoselected from the fetal rat gut: Expression of GFR alpha-1 in vitro and in vivo

机译:GDNF和NT-3对从胎鼠肠道免疫选择的神经c衍生前体中神经元和胶质细胞发育的影响的年龄依赖性差异:GFR alpha-1在体内和体外的表达

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No enteric neurons or glia develop in the gut below the rostral foregut in mice lacking glial cell line-derived neurotrophic factor (GDNF) or Ret. We analyzed the nature and age dependence of the effects of GDNF and, for comparison, those of NT-3, on the in vitro development of the precursors of enteric neurons and glia. Positive and negative immunoselection with antibodies to p75(NTR) were used to isolate crest-derived and crest-depleted populations of cells from the fetal rat bowel at E12, 14, and 16. Cells were typed immunocytochemically. GDNF stimulated the proliferation of nestin-expressing precursor cells isolated at E12, but not at E14-16. GDNF promoted the development of peripherin-expressing neurons (E12 much greater than E14-16) and expression of TrkC. GDNF inhibited expression of S-100-expressing glia at E14-16. NT-3 did not affect cells isolated at E12, never stimulated precursors to proliferate, and promoted glial as well as neuronal development at E14-16. GFR alpha-1 was expressed both by crest- and non-crest-derived cells, although only crest-derived cells anchored GFR alpha-1 and GFR alpha-2 (GFR alpha-1 much greater than GFR alpha-2). GDNF increased the number of neurons anchoring GFR alpha-1. GFR alpha-1 is immunocytochemically detectable in neurons of the E13 intestine and persists in adult neurons of both plexuses. We suggest that GDNF stimulates the proliferation of an early (E12) NT-3-insensitive precursor common to enteric neurons and glia; by E14, this common precursor is replaced by specified NT-3-responsive neuronal and glial progenitors. GDNF exerts a neurotrophic, but not a mitogenic, effect on the neuronal progenitor. The glial progenitor is not maintained by GDNF. (C) 1998 Academic Press. [References: 98]
机译:在缺乏胶质细胞系衍生的神经营养因子(GDNF)或Ret的小鼠中,在前额喙下方的肠道中没有肠神经元或胶质细胞发育。我们分析了GDNF和NT-3的作用对肠道神经元和神经胶质前体的体外发育的性质和年龄依赖性。使用针对p75(NTR)抗体的阳性和阴性免疫选择,从E12、14和16日从胎儿大鼠肠中分离出c来源的和c消除的细胞群。对细胞进行免疫细胞化学分型。 GDNF刺激在E12而非E14-16分离的表达巢蛋白的前体细胞的增殖。 GDNF促进表达外周蛋白的神经元(E12比E14-16大得多)和TrkC的表达。 GDNF抑制在E14-16处表达S-100的神经胶质细胞的表达。 NT-3不影响在E12分离的细胞,从不刺激前体增殖,并在E14-16促进神经胶质以及神经元发育。尽管只有alpha来源的细胞锚定了GFR alpha-1和GFR alpha-2(GFR alpha-1比GFR alpha-2大得多),但GFR alpha-1既可以由波峰来源的细胞表达,也可以由非波峰来源的细胞表达。 GDNF增加了锚定GFR alpha-1的神经元的数量。 GFR alpha-1在E13肠的神经元中可进行免疫细胞化学检测,并在两个丛的成年神经元中均存在。我们建议GDNF刺激肠神经元和神经胶质细胞常见的早期(E12)NT-3不敏感前体的增殖。通过E14,这种常见的前体被特定的NT-3反应神经元和神经胶质祖细胞所取代。 GDNF对神经元祖细胞产生神经营养作用,但不产生促有丝分裂作用。 GDNF不维持神经胶质祖细胞。 (C)1998年学术出版社。 [参考:98]

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