Proteinase-activated receptor-2 expression on cerebral neurones after radiation damage: immunohistochemical observation in Wistar rats.

T Olejár, R Matĕj, M Zadinová, P Poucková
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Abstract

Radiation damage results in blood-brain barrier damage followed by blood plasma transfer into the neuropil. The transferred liquid contains high amounts of biologically active substances/proteinases including factor Xa and a free pool of serum trypsin, which is not bound to antiproteases (alpha1 AT, alpha2-macroglobulin). The aim of this study was to follow up expression of proteinase-activated receptor-2 (PAR-2) in the brains of Wistar rats after single exposure to radiation at 26 Gy (60Co, 23 min, 15 sec). After irradiation, the animals were sacrificed on days 10, 20, 30 and 40. Control rat brains served as negative control. Coronal sections of caudal diencephalons were investigated using histology and immunohistochemistry. Polyclonal goat specified antibody against the NH-end of murine and rat PAR-2. Significant PAR-2 membrane positivity of scattered swollen neurons in deeper cortical layers was found in irradiated animals compared with controls. Although this membrane positivity was noticed in all irradiated animals, the most prominent occurred on day 30. Diffuse cytoplasmic positivity was also demonstrated on shrunken neurons in the cortex and hippocampus. Increased cytoplasmic and polarized membrane positivity was also noticed on the neurons of hypothalamic nuclei The causal relationship between blood-brain barrier damage, PAR-2 activation and neurodegeneration has not yet been verified. However, the present findings indicate that PAR-2 mediates a certain cellular response. It remains to be demonstrated whether this is a response to higher concentrations of factor Xa, a free pool of trypsin or other unknown possible proteinases in brain tissue; whether changes in PAR-2 expression are consequences of direct radiation damage to neuronal cells; whether this reaction is protective; and whether primary PAR-2 activation results in neuronal damage.

Wistar大鼠辐射损伤后脑神经元中蛋白酶活化受体-2表达的免疫组化观察。
辐射损伤导致血脑屏障损伤,随后血浆转移到神经细胞。转移的液体含有大量的生物活性物质/蛋白酶,包括Xa因子和一个自由的血清胰蛋白酶池,它不与抗蛋白酶(alpha1 AT, alpha2巨球蛋白)结合。本研究的目的是追踪Wistar大鼠在26 Gy (60Co, 23 min, 15 sec)单次辐照后大脑中蛋白酶活化受体-2 (PAR-2)的表达。辐照后于第10、20、30、40天处死。对照大鼠脑作为阴性对照。采用组织学和免疫组织化学方法对尾间脑冠状面切片进行研究。山羊特异性多克隆抗体,抗小鼠和大鼠PAR-2的nh端。与对照组相比,辐照动物皮层深层分散肿胀神经元PAR-2膜明显阳性。虽然在所有受辐射动物中都发现了这种膜阳性,但在第30天最明显。皮层和海马的萎缩神经元也表现出弥漫性细胞质阳性。下丘脑核神经元的细胞质和极化膜阳性也增加。血脑屏障损伤、PAR-2激活与神经退行性变之间的因果关系尚未得到证实。然而,目前的研究结果表明PAR-2介导一定的细胞反应。这是否是对更高浓度的Xa因子、胰蛋白酶的自由池或脑组织中其他未知的可能的蛋白酶的反应,还有待证明;PAR-2表达的变化是否是直接辐射损伤神经元细胞的结果;这个反应是否具有保护性;以及原发性PAR-2激活是否会导致神经元损伤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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