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首页> 外文期刊>Journal of Neurocytology: A Journal of Cellular Neurobiology >Developmental expression of neurotrophin receptor genes in rat geniculate ganglion neurons.
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Developmental expression of neurotrophin receptor genes in rat geniculate ganglion neurons.

机译:神经营养蛋白受体基因在大鼠膝状神经节神经元中的发育表达。

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Individual neurons dissected from immunohistochemically stained paraffin sections of the developing rat geniculate (VIIth cranial) ganglion were assayed for their content of mRNA of the neurotrophin receptor genes, p75 , trkA , trkB and trkC. Fetal and postnatal rats, from the 13th embryonic day (E13) until the 20th postnatal day (P20), were used. Single cells were subjected to RNA amplification, followed by treatment with reverse transcriptase and DNA amplification by the polymerase chain reaction (PCR). The identity of the PCR products was verified by subcloning and sequencing. A total of 227 neurons were examined, of which 212 (93%) gave a PCR signal for at least one neurotrophin receptor. We found: (1) Approximately half of the neurons expressed more than one receptor. (2) A truncated version of trkB , possessing the ligand-binding region but lacking the tyrosine kinase domain, occurred quite frequently, often in combination with the full-length trkB, with trkA or both. (3) The pattern of staining for trkB-like immunoreactivity was usually predictive that either its full length or truncated mRNA would be present. This was not the case for trkC-like immunoreactivity. Western blots on E15 brain tissue showed no band for full-length trkC ( approximately 150 kDa), suggesting the antibody may have been immunoreactive with a truncated ( approximately 120 kDa) but not a full-length version of the trkC receptor. (4) The pattern of neurotrophin receptor gene expression changed during development. (5) p75 expression occurred infrequently-in only 7 of the 212 neurons that gave a signal for any receptor.
机译:从发育中的大鼠膝状神经节(第七颅神经节)的免疫组织化学染色的石蜡切片中分离出的单个神经元,测定其神经营养蛋白受体基因p75,trkA,trkB和trkC的mRNA含量。使用从胚胎第13天(E13)到出生后20天(P20)的胎鼠和产后鼠。对单细胞进行RNA扩增,然后通过聚合酶链反应(PCR)用逆转录酶处理和DNA扩增。通过亚克隆和测序验证PCR产物的身份。共检查了227个神经元,其中212个(93%)提供了至少一种神经营养蛋白受体的PCR信号。我们发现:(1)大约一半的神经元表达一种以上的受体。 (2)具有配体结合区但缺乏酪氨酸激酶结构域的trkB的截短形式经常发生,通常与全长trkB,trkA或两者结合使用。 (3)trkB样免疫反应性染色的模式通常可以预测其全长或截短的mRNA的存在。 trkC样免疫反应性并非如此。 E15脑组织上的蛋白质印迹未显示全长trkC(约150 kDa)的条带,表明该抗体可能与截短的(约120 kDa)具有免疫反应性,但不是全长版本的trkC受体具有免疫反应性。 (4)神经营养蛋白受体基因表达的模式在发育过程中发生了变化。 (5)p75表达很少发生-在212个神经元中只有7个能发出任何受体信号。

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