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衰老对大鼠肝窦内皮细胞中 VEGF/VEGFR2 信号通路基因表达的影响。

The effect of aging on VEGF/VEGFR2 signal pathway genes expression in rat liver sinusoidal endothelial cell.

机构信息

Department of Hepatobiliary Surgery, First Affiliated Hospital, Xi'an Jiaotong University, No.277 West Yanta Road, Xi'an, 710061, Shaanxi, People's Republic of China.

Department of General Surgery, Bazhong Central Hospital, No.1 Nanchi River Street, Bazhong, 636000, Sichuan, People's Republic of China.

出版信息

Mol Cell Biochem. 2021 Jan;476(1):269-277. doi: 10.1007/s11010-020-03903-7. Epub 2020 Sep 12.

Abstract

Liver sinusoidal endothelial cells (LSECs) play a key role in the initiation and neoangiogenesis of liver regeneration. We presume that the abnormity of the VEGF/VEGFR2 and its pathway gene Id1, Wnt2 and HGF expression in aged LSECs may be an important mechanism to affect liver regeneration of the elderly. LSECs from two different groups (adult and old) were isolated in a rodent model, and observed by SEM and TEM. The adult and old rats were underwent 70% partial hepatectomy. The proliferation of hepatocytes and LSECs were analyzed by Immunofluorescence staining. The expression of VEGF/VEGFR2 and its pathway gene in isolated LSECs and liver tissue after hepatectomy were detected by qRT-PCR and Western blot. There is a decreased number of endothelial fenestrae in the LSECs of the old group, compared to the adult group. The old group had a lower expression of VEGF/VEGFR2 and its pathway gene than the adult groups (p < 0.01). The results of western blot were consistent with those of qRT-PCR. The hepatocytes had a high proliferation rate at first 4 days after hepatectomy, and a significantly higher proliferation rate in the adult group. The LSECs began to proliferate after 4 days of hepatectomy, and showed a quantity advantage in the adult group. The adult group had a significantly higher expression of VEGF/VEGFR2 and its pathway gene after hepatectomy than the old group (p < 0.01). LSCEs turn to be defenestration in structure and have a low expression of VEGF/VEGFR2 and its pathway gene with aging.

摘要

肝窦内皮细胞(LSEC)在肝脏再生的启动和新生血管形成中起关键作用。我们推测,衰老 LSEC 中 VEGF/VEGFR2 及其通路基因 Id1、Wnt2 和 HGF 表达的异常可能是影响老年人肝脏再生的重要机制。在啮齿动物模型中分离两组(成年和老年)的 LSEC,并通过 SEM 和 TEM 进行观察。成年和老年大鼠接受 70%部分肝切除术。通过免疫荧光染色分析肝细胞和 LSEC 的增殖。通过 qRT-PCR 和 Western blot 检测肝切除后分离的 LSEC 和肝组织中 VEGF/VEGFR2 及其通路基因的表达。与成年组相比,老年组 LSEC 的内皮窗孔数量减少。老年组 VEGF/VEGFR2 及其通路基因的表达低于成年组(p<0.01)。Western blot 的结果与 qRT-PCR 的结果一致。肝细胞在肝切除后最初 4 天内增殖率较高,且成年组的增殖率显著更高。LSEC 在肝切除后 4 天开始增殖,并在成年组中表现出数量优势。肝切除后成年组 VEGF/VEGFR2 及其通路基因的表达明显高于老年组(p<0.01)。随着年龄的增长,LSCEs 的结构变得无窗孔,并且 VEGF/VEGFR2 及其通路基因的表达降低。

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