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干性相关标志物在颅外动静脉畸形中表达。

Stemness-Associated Markers Are Expressed in Extracranial Arteriovenous Malformation.

作者信息

Luke Krishnan Claire S, Brasch Helen D, Patel Josie, Bockett Nicholas, Paterson Erin, Davis Paul F, Tan Swee T

机构信息

Gillies McIndoe Research Institute, Wellington, New Zealand.

Centre for the Study & Treatment of Vascular Birthmarks, Wellington Regional Plastic, Maxillofacial and Burns Unit, Hutt Hospital, Wellington, New Zealand.

出版信息

Front Surg. 2021 Mar 19;8:621089. doi: 10.3389/fsurg.2021.621089. eCollection 2021.

Abstract

Arteriovenous malformation (AVM) consists of a with poorly formed low-resistance vessels in place of a functional capillary network. The role of somatic mutations in embryonic stem cells (ESCs) and vascular anomalies and the presence of primitive populations in vascular anomalies led us to investigate the presence of a primitive population in extracranial AVM. Extracranial AVM tissue samples from 12 patients were stained for stemness-associated markers OCT4, SOX2, NANOG, KLF4, and c-MYC using immunohistochemical staining. hybridization (ISH) was performed on six tissue samples to determine transcript expression. Western blotting and RT-qPCR were performed on two AVM-derived primary cell lines to determine protein and transcript expression of these markers, respectively. Immunofluorescence staining was performed on two tissue samples to investigate marker co-localization. Immunohistochemical staining demonstrated the expression of OCT4, SOX2, KLF4, and c-MYC on the endothelium and media of lesional vessels and cells within the stroma of the in all 12 AVM tissue samples. ISH and RT-qPCR confirmed transcript expression of all five markers. Western blotting showed protein expression of all markers except NANOG. Immunofluorescence staining demonstrated an OCT4+/SOX2+/KLF4+/c-MYC+ population within the endothelium and media of the lesional vessels and cells within the stroma of the AVM . Our findings may suggest the presence of a primitive population within the AVM . Further investigation may lead to novel therapeutic targeting of this population.

摘要

动静脉畸形(AVM)由一组发育不良的低阻力血管组成,取代了功能性毛细血管网络。体细胞突变在胚胎干细胞(ESC)和血管异常中的作用以及血管异常中原始细胞群的存在,促使我们研究颅外AVM中原始细胞群的存在情况。使用免疫组织化学染色法,对12例患者的颅外AVM组织样本进行干性相关标志物OCT4、SOX2、NANOG、KLF4和c-MYC染色。对6个组织样本进行原位杂交(ISH)以确定转录本表达。对两个源自AVM的原代细胞系进行蛋白质免疫印迹和逆转录定量聚合酶链反应(RT-qPCR),分别确定这些标志物的蛋白质和转录本表达。对两个组织样本进行免疫荧光染色以研究标志物的共定位。免疫组织化学染色显示,在所有12个AVM组织样本中,病变血管的内皮和中膜以及AVM间质内的细胞均表达OCT4、SOX2、KLF4和c-MYC。ISH和RT-qPCR证实了所有5种标志物的转录本表达。蛋白质免疫印迹显示除NANOG外所有标志物的蛋白质表达。免疫荧光染色显示AVM病变血管的内皮和中膜以及间质内的细胞中有一个OCT4+/SOX2+/KLF4+/c-MYC+细胞群。我们的研究结果可能提示AVM中存在原始细胞群。进一步的研究可能会导致针对该细胞群的新型治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8060/8017302/4b7c6cb26325/fsurg-08-621089-g0001.jpg

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