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α-SMA 阳性血管壁细胞抑制血管母细胞瘤中的囊肿形成。

α-SMA positive vascular mural cells suppress cyst formation in hemangioblastoma.

机构信息

Department of Neurosurgery, Graduate School of Medical Science, Kanazawa University, 13-1 Takara-Machi, Kanazawa, 920-8641, Japan.

Department of Diagnostic Pathology, Kanazawa University Hospital, Kanazawa, Japan.

出版信息

Brain Tumor Pathol. 2023 Jul;40(3):176-184. doi: 10.1007/s10014-023-00465-6. Epub 2023 Jun 5.

Abstract

Approximately 60% of hemangioblastomas (HBs) have peritumoral cysts adjacent to the tumor, which can cause neurological deficits due to the mass effect, and the management of cyst formation is a clinical challenge. Vascular mural cells surrounding endothelial cells consist of vascular smooth muscle cells (vSMCs) and pericytes, which are essential elements that support blood vessels and regulate permeability. This study investigated the involvement of mural cells in cyst formation. We analyzed the expression of α-smooth muscle actin (α-SMA), platelet-derived growth factor receptor-beta (PDGFRB), and CD31 in 39 consecutive human cerebellar HBs, 20 of cystic and 19 of solid type. Solid type HBs showed stronger diffuse expression of α-SMA in precapillary arterioles and capillaries within the tumor than cystic type HBs (p = 0.001), whereas there was no difference in PDGFRB and CD31 expression. Detailed observation with immunofluorescence demonstrated that α-SMA was expressed in vascular mural cells surrounding capillaries in the solid rather than in the cystic type. Multivariate analysis including various clinical and pathological factors showed that lower α-SMA expression was significantly correlated with cyst formation (p < 0.001). Our data suggested that vascular mural cells from precapillary arterioles to capillaries expressing α-SMA may be pericytes and play a crucial role in HB cystogenesis.

摘要

约 60%的血管母细胞瘤(HB)旁有肿瘤周围囊肿,由于占位效应可导致神经功能缺损,而囊肿形成的处理是临床挑战。围绕内皮细胞的血管壁细胞由血管平滑肌细胞(vSMCs)和周细胞组成,是支持血管和调节通透性的重要元素。本研究探讨了壁细胞在囊肿形成中的作用。我们分析了 39 例连续的人小脑 HB 中 α-平滑肌肌动蛋白(α-SMA)、血小板衍生生长因子受体-β(PDGFRB)和 CD31 的表达,其中囊性 20 例,实体型 19 例。与囊性 HB 相比,实体型 HB 在肿瘤内毛细血管前小动脉和毛细血管中显示出更强的 α-SMA 弥漫性表达(p=0.001),而 PDGFRB 和 CD31 表达无差异。免疫荧光的详细观察表明,α-SMA 表达在实体型而不是囊性 HB 中围绕毛细血管的血管壁细胞。包括各种临床和病理因素的多变量分析表明,α-SMA 表达降低与囊肿形成显著相关(p<0.001)。我们的数据表明,从毛细血管前小动脉到毛细血管表达 α-SMA 的血管壁细胞可能是周细胞,并在 HB 囊肿形成中起关键作用。

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