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首页> 外文期刊>Brain research >Basic fibroblast growth factor (bFGF) injection activates the glial reaction in the injured adult rat brain.
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Basic fibroblast growth factor (bFGF) injection activates the glial reaction in the injured adult rat brain.

机译:碱性成纤维细胞生长因子(bFGF)注射激活了成年大鼠大脑中的神经胶质反应。

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摘要

Reactive gliosis is a reaction of glial cells to trauma which is characterized by a phenotypic modification of astrocytes, as well as by a proliferation and a migration of some of these cells to form a glial scar. This scar is currently considered as a physical impediment to neuronal regrowth but it may also be involved in wound healing since the astrocytes beside microglia play a phagocytic role in the clearance of post-traumatic debris. Growth factors are released in the area of the injury and at least some of them could be involved in gliosis. In order to test directly this possibility, we have injected one of them, the basic fibroblast growth factor (bFGF), into several brain areas (cortex, striatum, hippocampus or corpus callosum) of adult 2-month-old rats in the absence of lesion. A glial reaction was observed after 3 days and was maximum after 7 days. It was characterized by an increase in astrocyte proliferation and in glial fibrillary acidic protein (GFAP) expression, resulting in a higher number of GFAP-positive cells per surface unit, and by an increase in the size and branching of the astroglial processes. The GFAP mRNA levels were also strongly increased following the bFGF injection. These effects resemble the reactive gliosis observed after lesion and suggest that bFGF is actually involved in the triggering of glial reactions which follow brain injury. In further experiments, bFGF was injected in the site of electrolytic lesions made in the same various parts of the brain. These injections did not increase significantly the normal reactive gliosis induced by the lesion alone, but it accelerated some of the effects. It also resulted in a higher labeling index and GFAP mRNA levels were strongly enhanced after a 3-day-post-operative delay. This last observation strengthens the idea that one of the main factors driving the astrogliosis is the bFGF normally released in and around the site of the lesion.
机译:反应性神经胶质增生是神经胶质细胞对创伤的反应,其特征在于星形胶质细胞的表型修饰,以及某些细胞的增殖和迁移以形成神经胶质瘢痕。该疤痕目前被认为是神经元再生的物理障碍,但由于小胶质细胞旁的星形胶质细胞在清除创伤后碎片中具有吞噬作用,因此它也可能参与伤口愈合。生长因子在损伤区域释放,其中至少一些可能与胶质增生有关。为了直接测试这种可能性,我们在不存在2个月大的成年大鼠的情况下,将其中一种,即碱性成纤维细胞生长因子(bFGF)注入了成年2个月大大鼠的几个大脑区域(皮层,纹状体,海马或体)中。病变。 3天后观察到神经胶质反应,7天后达到最大。其特征是星形胶质细胞增殖和神经胶质原纤维酸性蛋白(GFAP)表达增加,从而导致每个表面单位的GFAP阳性细胞数量增加,以及星形胶质细胞过程的大小和分支增加。 bFGF注射后,GFAP mRNA水平也大大增加。这些作用类似于病变后观察到的反应性神经胶质增生,提示bFGF实际上参与了脑损伤后神经胶质反应的触发。在进一步的实验中,将bFGF注射到大脑各个部位的电解损伤部位。这些注射并没有显着增加仅由病变引起的正常反应性神经胶质增生,但是加速了某些作用。这也导致更高的标记指数,术后3天延迟后GFAP mRNA水平显着提高。最后的观察结果强化了这样一种观念,即驱动星形胶质细胞增生的主要因素之一是通常在病变部位及其周围释放的bFGF。

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