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神经营养因子受体酪氨酸激酶(TrkA、TrkB、TrkC)mRNA在结状神经节和岩神经节内脏传入神经元中的存在及定位。

Presence and localization of neurotrophin receptor tyrosine kinase (TrkA, TrkB, TrkC) mRNAs in visceral afferent neurons of the nodose and petrosal ganglia.

作者信息

Zhuo H, Helke C J

机构信息

Department of Pharmacology, Uniformed Services University of the Health Sciences, Bethesda, MD 20814, USA.

出版信息

Brain Res Mol Brain Res. 1996 May;38(1):63-70. doi: 10.1016/0169-328x(95)00313-h.

Abstract

The presence of mRNAs to the high affinity tyrosine kinase (Trk) receptors for neurotrophins was studied in visceral afferent neurons of the nodose and petrosal ganglia of adult and neonatal rats using in situ hybridization histochemistry. Neurons containing TrkA mRNA were found in the adult nodose and petrosal ganglia. About 10% of nodose ganglion neurons and 38% of petrosal ganglion neurons contained TrkA mRNA. The nodose and petrosal ganglia from 1 day old neonates also expressed TrkA mRNA. No TrkB mRNA-containing neurons were detected in the adult nodose and petrosal ganglia, whereas TrkB mRNA was detected in 1 day old neonatal nodose and petrosal ganglia. TrkC mRNA was found in about 9% of nodose ganglion neurons and 11% of petrosal ganglion neurons of adult rats. Likewise, low but detectable levels of TrkC mRNA were seen in 1 day old neonatal nodose and petrosal ganglia. These data demonstrate the presence of TrkA and TrkC in the adult nodose and petrosal ganglia and provide a substrate for the ongoing neurotrophin-induced regulation of these placodally derived visceral afferent neurons. The altered expression of Trk receptor mRNAs in the nodose and petrosal ganglia between the adult and neonatal rats may reflect developmentally regulated changes in neurotrophin responsiveness.

摘要

利用原位杂交组织化学技术,研究了成年和新生大鼠结节神经节及岩神经节内脏传入神经元中神经营养因子高亲和力酪氨酸激酶(Trk)受体的mRNA表达情况。在成年大鼠的结节神经节和岩神经节中发现了含有TrkA mRNA的神经元。约10%的结节神经节神经元和38%的岩神经节神经元含有TrkA mRNA。出生1天的新生大鼠的结节神经节和岩神经节也表达TrkA mRNA。在成年大鼠的结节神经节和岩神经节中未检测到含有TrkB mRNA的神经元,而在出生1天的新生大鼠的结节神经节和岩神经节中检测到了TrkB mRNA。在成年大鼠约9%的结节神经节神经元和11%的岩神经节神经元中发现了TrkC mRNA。同样,在出生1天的新生大鼠的结节神经节和岩神经节中也观察到了低水平但可检测到的TrkC mRNA。这些数据表明成年大鼠的结节神经节和岩神经节中存在TrkA和TrkC,并为神经营养因子对这些源自基板的内脏传入神经元的持续调节提供了基础。成年和新生大鼠结节神经节及岩神经节中Trk受体mRNA表达的改变可能反映了神经营养因子反应性的发育调控变化。

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