Brn-3a deficiency increases tyrosine hydroxylase-immunoreactive neurons in the dorsal root ganglion.

Brn-3a deficiency increases tyrosine hydroxylase-immunoreactive neurons in the dorsal root ganglion.
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Brn-3a 缺乏会增加背根神经节中酪氨酸羟化酶免疫反应性神经元。

DOI:
10.1016/j.brainres.2004.10.028
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发表时间:
2005
期刊:
Brain research.
影响因子:
--
通讯作者:
Sugimoto,Tomosada
Sugimoto,Tomosada
中科院分区:
--
文献类型:
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作者:
Ichikawa,Hiroyuki;Mo,Zeqian;Xiang,Mengqing;Sugimoto,Tomosada

文献摘要

相似文献

酪氨酸羟化酶(TH)的免疫组织化学进行野生型,杂合子和Brn-3a基因敲除小鼠在胚胎第18.5天的背根神经节(DRG)。TH-免疫反应(-IR)神经元中检测到的野生型和杂合子小鼠的背根节,但其比例大大增加的Brn-3a功能的损失(野生型和杂合子,8.4%;敲除,20.9%)。野生型IR神经元的大小不同(平均值± SD = 118.1 ± 55.4 μm2,范围= 26.6-306.3 μm2)和杂合子小鼠。然而,在基因敲除小鼠中,TH-1 R神经元大多较小(平均值± S.D. = 68.2 ± 34.3 μm2,范围= 11.8-166.8 μm2)。目前的研究表明,Brn-3a可能在正常情况下抑制许多小DRG神经元中的TH表达,但激活大DRG神经元中的TH表达。
Immunohistochemistry for tyrosine hydroxylase (TH) was performed on the dorsal root ganglia (DRG) in wild-type, heterozygous and Brn-3a knockout mice at embryonic day 18.5. TH-immunoreactive (-IR) neurons were detected in the DRG of wild-type and heterozygous mice, but their proportion was greatly increased by the loss of Brn-3a function (wild-type and heterozygot, 8.4%; knockout, 20.9%). IR neurons were of various sizes in wild-type (mean ± S.D. = 118.1 ± 55.4 μm2, range = 26.6–306.3 μm2) and heterozygous mice. In the knockout mice, however, TH-IR neurons were mostly small (mean ± S.D. = 68.2 ± 34.3 μm2, range = 11.8–166.8 μm2). The present study suggests that Brn-3a may normally suppress TH expression in many small DRG neurons but activate TH expression in large DRG neurons.