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腺病毒介导的 NR5A1 过表达将人脂肪组织来源的间充质基质细胞分化为类固醇生成细胞,并植入肾上腺功能不全的小鼠体内。

Differentiation of human adipose tissue-derived mesenchymal stromal cells into steroidogenic cells by adenovirus-mediated overexpression of NR5A1 and implantation into adrenal insufficient mice.

机构信息

Department of Regenerative Medicine and Transplantation, Faculty of Medicine, Fukuoka University, Fukuoka, Japan; Department of Urology, Faculty of Medicine, Fukuoka University, Fukuoka, Japan.

Department of Regenerative Medicine and Transplantation, Faculty of Medicine, Fukuoka University, Fukuoka, Japan.

出版信息

Cytotherapy. 2023 Aug;25(8):866-876. doi: 10.1016/j.jcyt.2023.04.002. Epub 2023 May 5.

Abstract

BACKGROUND AIMS

Cell therapy for adrenal insufficiency is a potential method for physiological glucocorticoid and mineralocorticoid replacement. We have previously shown that mouse mesenchymal stromal cells (MSCs) differentiated into steroidogenic cells by the viral vector-mediated overexpression of nuclear receptor subfamily 5 group A member 1 (NR5A1), an essential regulator of steroidogenesis, and their implantation extended the survival of bilateral adrenalectomized (bADX) mice.

METHODS

In this study, we examined the capability of NR5A1-induced steroidogenic cells prepared from human adipose tissue-derived MSCs (MSC [AT]) and the therapeutic effect of the implantation of human NR5A1-induced steroidogenic cells into immunodeficient bADX mice.

RESULTS

Human NR5A1-induced steroidogenic cells secreted adrenal and gonadal steroids and exhibited responsiveness to adrenocorticotropic hormone and angiotensin II in vitro. In vivo, the survival time of bADX mice implanted with NR5A1-induced steroidogenic cells was significantly prolonged compared with that of bADX mice implanted with control MSC (AT). Serum cortisol levels, which indicate hormone secretion from the graft, were detected in bADX mice implanted with steroidogenic cells.

CONCLUSIONS

This is the first report to demonstrate steroid replacement by the implantation of steroid-producing cells derived from human MSC (AT). These results indicate the potential of human MSC (AT) to be a source of steroid hormone-producing cells.

摘要

背景目的

细胞疗法治疗肾上腺功能不全是一种生理糖皮质激素和盐皮质激素替代的潜在方法。我们之前已经表明,通过病毒载体介导的核受体亚家族 5 组 A 成员 1(NR5A1)的过表达,将小鼠间充质基质细胞(MSCs)分化为类固醇生成细胞,NR5A1 是类固醇生成的必需调节剂,它们的植入延长了双侧肾上腺切除术(bADX)小鼠的存活时间。

方法

在这项研究中,我们检查了从人脂肪组织来源的 MSC(MSC [AT])制备的 NR5A1 诱导的类固醇生成细胞的能力,以及将人 NR5A1 诱导的类固醇生成细胞植入免疫缺陷 bADX 小鼠中的治疗效果。

结果

人 NR5A1 诱导的类固醇生成细胞分泌肾上腺和性腺类固醇,并在体外对促肾上腺皮质激素和血管紧张素 II 有反应。在体内,与植入对照 MSC(AT)的 bADX 小鼠相比,植入 NR5A1 诱导的类固醇生成细胞的 bADX 小鼠的存活时间明显延长。植入类固醇生成细胞的 bADX 小鼠中检测到表明移植物激素分泌的血清皮质醇水平。

结论

这是首例报道植入源自人 MSC(AT)的产生类固醇的细胞可进行类固醇替代的报告。这些结果表明人 MSC(AT)有可能成为产生类固醇激素的细胞来源。

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