Entorhinal deafferentation induces upregulation of SPARC in the mouse hippocampus

Xin Liu, Guoxin Ying, Wenyuan Wang, Jinghui Dong, Yan Wang, Zimei Ni, Changfu Zhou
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引用次数: 21

Abstract

SPARC is a matricellular protein that modulates cell–cell and cell–matrix interactions by virtue of its antiproliferative and counteradhesive properties. Here, we report the denervation-induced upregulation of SPARC mRNA and protein in the mouse hippocampus following transections of the entorhinal afferents. Northern blot analysis showed that SPARC mRNA was upregulated in a transient manner in the deafferented mouse hippocampus. In situ hybridization and immunohistochemistry confirmed the temporal upregulation of both SPARC mRNA and protein specifically in the denervated areas, which initiated at 7 days postlesion, reached the maximum at 15 as well as 30 days postlesion, and subsided towards normal levels by 60 days postlesion. Double labeling by either a combination of in situ hybridization for SPARC mRNA with immunohistochemistry for glial fibrillary acidic protein or double immunofluorescence staining for both proteins in the hippocampus revealed that SPARC-expressing cells are reactive astrocytes. In respect to the spatiotemporal alterations of SPARC expression in the denervated hippocampus, we suggest that SPARC may be involved in modulation of the denervation-induced plasticity processes such as glial cell proliferation, axonal sprouting and subsequent synaptogenesis in the hippocampus following entorhinal deafferentation.

内嗅脱神经诱导小鼠海马中SPARC的上调
SPARC是一种基质细胞蛋白,通过其抗增殖和抗粘附特性调节细胞-细胞和细胞-基质相互作用。在这里,我们报道了在小鼠内嗅传入神经横断后,去神经刺激诱导的小鼠海马中SPARC mRNA和蛋白的上调。Northern blot分析显示,在失神经元化小鼠海马中,SPARC mRNA呈短暂性上调。原位杂交和免疫组织化学证实,去神经区SPARC mRNA和蛋白的时间特异性上调始于病变后7天,在病变后15天和30天达到最大,并在病变后60天回落至正常水平。通过对SPARC mRNA的原位杂交和对胶质纤维酸性蛋白的免疫组织化学或对海马中两种蛋白的双重免疫荧光染色的双重标记,表明表达SPARC的细胞是反应性星形胶质细胞。关于SPARC在去神经支配海马中表达的时空变化,我们认为SPARC可能参与调节去神经支配诱导的可塑性过程,如神经胶质细胞增殖、轴突发芽和随后的海马突触形成。
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