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克氏综合征患者外周血单个核细胞中的基因下调。

gene downregulation in peripheral blood mononuclear cells of patients with Klinefelter syndrome.

机构信息

Department of Clinical and Experimental Medicine, University of Catania, Catania 95123, Italy.

Oasi Research Institute-IRCCS, Troina (EN) 94018, Italy.

出版信息

Asian J Androl. 2021 Mar-Apr;23(2):157-162. doi: 10.4103/aja.aja_37_20.

Abstract

Klinefelter syndrome (KS) is the most common sex chromosome disorder in men. It is characterized by germ cell loss and other variable clinical features, including autoimmunity. The sex-determining region of Y (SRY)-box 13 (Sox13) gene is expressed in mouse spermatogonia. In addition, it has been identified as islet cell autoantigen 12 (ICA12), which is involved in the pathogenesis of autoimmune diseases, including type 1 diabetes mellitus (DM) and primary biliary cirrhosis. Sox13 expression has never been investigated in patients with KS. In this age-matched, case-control study performed on ten patients with KS and ten controls, we found that SOX13 is significantly downregulated in peripheral blood mononuclear cells of patients with KS compared to controls. This finding might be consistent with the germ cell loss typical of patients with KS. However, the role of Sox13 in the pathogenesis of germ cell loss and humoral autoimmunity in patients with KS deserves to be further explored.

摘要

克氏综合征(KS)是男性最常见的性染色体疾病。其特征是生殖细胞丢失和其他可变的临床特征,包括自身免疫。Y 染色体性别决定区(SRY)-盒 13(Sox13)基因在小鼠精原细胞中表达。此外,它已被确定为胰岛细胞自身抗原 12(ICA12),这涉及到包括 1 型糖尿病(DM)和原发性胆汁性肝硬化在内的自身免疫性疾病的发病机制。Sox13 的表达从未在 KS 患者中进行过研究。在这项对 10 名 KS 患者和 10 名对照进行的年龄匹配病例对照研究中,我们发现与对照组相比,KS 患者外周血单核细胞中的 SOX13 显著下调。这一发现可能与 KS 患者典型的生殖细胞丢失一致。然而,Sox13 在 KS 患者生殖细胞丢失和体液自身免疫发病机制中的作用值得进一步探讨。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60d7/7991811/426691eee182/AJA-23-157-g001.jpg

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