应用非放射性原位杂交组织化学和免疫组织化学同时检测大细胞下丘脑-神经垂体系统中的神经肽和信使RNA。

Histochemistry Pub Date : 1994-12-01 DOI:10.1007/BF00269572
P J Larsen, J D Mikkelsen
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引用次数: 4

摘要

采用非放射性原位杂交组织化学与酶免疫组织化学相结合的方法,检测表型神经元中mRNA的表达。用生物素-11- dutp标记的3'端寡核苷酸探针杂交自由浮动脑切片。以二氨基联苯胺为底物,采用亲和素-生物素桥法、抗亲和素免疫组化和辣根过氧化物酶检测相结合的方法对杂交探针进行可视化。原位杂交步骤产生了一个非常稳定的反应产物,使随后的免疫组织化学反应使用辣根过氧化物酶和盐酸联苯胺作为显色剂。下丘脑-神经生理系统的大细胞神经元合成抗利尿激素或催产素;缺水和长期摄入生理盐水是编码这些神经肽的两种基因表达的有力刺激。在这样的刺激过程中,大细胞神经元中合成了许多其他具有递质作用的神经肽。通过实验探讨下丘脑-神经物理系统中表达抗利尿激素mrna的大细胞神经元中是否存在神经肽Y免疫反应性。结果清楚地表明,神经肽y免疫反应元件存在于一些大细胞抗利尿激素mrna含有细胞。此外,免疫组化检测抗利尿激素非放射性杂交切片的神经肽催产素和胆囊收缩素;正如预期的那样,抗利尿激素mRNA并不与胆囊收缩素共存,而在渗透刺激的动物中,一些催产素免疫反应神经元也含有抗利尿激素mRNA。所开发的方法使细胞内抗原的免疫组织化学检测与细胞内mRNA的检测成为可能。
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Simultaneous detection of neuropeptides and messenger RNA in the magnocellular hypothalamo-neurohypophysial system by a combination of non-radioactive in situ hybridization histochemistry and immunohistochemistry.

A protocol was developed combining non-radioactive in situ hybridization histochemistry with enzyme based immunohistochemistry, detect the expression of mRNA in phenotypically defined neurons. Free-floating brain sections were hybridized with the oligonucleotide probes which have been 3'-end labelled with biotin-11-dUTP. The hybridized probe was visualized by a combined avidin-biotin bridge method, anti-avidin immunohistochemistry, and horseradish peroxidase detection using diaminobenzidine as a substrate. The in situ hybridization step yielded a very stable reaction product enabling subsequent immunohistochemical reactions using horseradish peroxidase and benzidine dihydrochloride as a chromogen. Magnocellular neurons of the hypothalamo-neurophypophysial system synthesize either vasopressin or oxytocin; water deprivation and chronic saline ingestion are potent stimuli for the expression of both of the genes encoding these neuropeptides. A number of other neuropeptides with putative transmitter action are synthesized in magnocellular neurons during such stimulation. Experiments were performed to explore whether neuropeptide Y immunoreactivity is present within magnocellular vasopressin mRNA-expressing neurons of the hypothalamo-neurophypophysial system. The results clearly demonstrated that neuropeptide Y-immunoreactive elements were present within a number of magnocellular vasopressin mRNA-containing cells. In addition, immunohistochemical detection of the neuropeptides ocytocin and cholecystokinin was carried out on sections hybridized non-radioactively for vasopressin; as expected vasopressin mRNA did not co-exist with cholecystokinin, whereas a few oxytocin immunoreactive neurons in osmotically stimulated animals also contained vasopressin mRNA. The developed method makes possible the immunohistochemical detection of intracellular antigens with concomitant detection of intracellular mRNA.

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