9-cis-retinoic acid signaling in Sertoli cells regulates their immunomodulatory function to control lymphocyte physiology and Treg differentiation.

IF 4.2 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM Reproductive Biology and Endocrinology Pub Date : 2024-06-26 DOI:10.1186/s12958-024-01246-2
Alicja Kamińska, Laura Pardyak, Sylwia Lustofin, Karolina Gielata, Zbigniew Arent, Agnieszka Pietsch-Fulbiszewska, Anna Hejmej
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Abstract

Background: Testis is an immune privileged organ, which prevents the immune response against sperm antigens and inflammation. Testicular cells responsible for immune tolerance are mainly Sertoli cells, which form the blood-testis barrier and produce immunosuppressive factors. Sertoli cells prevent inflammation in the testis and maintain immune tolerance by inhibiting proliferation and inducing lymphocyte apoptosis. It has been shown that 9-cis-retinoic acid (9cRA) blocks ex vivo apoptosis of peripheral blood lymphocytes and promotes the differentiation of Treg cells in the gut. However, the role of retinoid signaling in regulating the immune privilege of the testes remains unknown.

Objective: The aim of this study was to determine whether 9cRA, acting via the retinoic acid receptors (RAR) and the retinoic X receptors (RXR), controls the immunomodulatory functions of Sertoli cells by influencing the secretion of anti-inflammatory/pro-inflammatory factors, lymphocyte physiology and Treg cell differentiation.

Methods: Experiments were performed using in vitro model of co-cultures of murine Sertoli cells and T lymphocytes. Agonists and antagonists of retinoic acid receptors were used to inhibit/stimulate retinoid signaling in Sertoli cells.

Results: Our results have demonstrated that 9cRA inhibits the expression of immunosuppressive genes and enhances the expression of pro-inflammatory factors in Sertoli cells and lymphocytes, increases lymphocyte viability and decreases apoptosis rate. Moreover, we have found that 9cRA blocks lymphocyte apoptosis acting through both RAR and RXR and inhibiting FasL/Fas/Caspase 8 and Bax/Bcl-2/Caspase 9 pathways. Finally, we have shown that 9cRA signaling in Sertoli cells inhibits Treg differentiation.

Conclusion: Collectively, our results indicate that retinoid signaling negatively regulates immunologically privileged functions of Sertoli cells, crucial for ensuring male fertility. 9cRA inhibits lymphocyte apoptosis, which can be related to the development of autoimmunity, inflammation, and, in consequence, infertility.

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Sertoli细胞中的9-顺式维甲酸信号调节其免疫调节功能,从而控制淋巴细胞的生理学和Treg分化。
背景:睾丸是一个免疫特权器官,可防止针对精子抗原和炎症的免疫反应。负责免疫耐受的睾丸细胞主要是 Sertoli 细胞,它们构成血液-睾丸屏障并产生免疫抑制因子。Sertoli 细胞通过抑制增殖和诱导淋巴细胞凋亡来防止睾丸发炎并维持免疫耐受。研究表明,9-顺式维甲酸(9cRA)可阻止外周血淋巴细胞的体内凋亡,并促进肠道中 Treg 细胞的分化。然而,视黄酸信号在调节睾丸免疫特权中的作用仍然未知:本研究旨在确定9cRA是否通过视黄酸受体(RAR)和视黄酸X受体(RXR)发挥作用,通过影响抗炎/促炎因子的分泌、淋巴细胞生理机能和Treg细胞分化来控制Sertoli细胞的免疫调节功能:实验采用小鼠 Sertoli 细胞和 T 淋巴细胞共培养的体外模型。方法:实验采用小鼠 Sertoli 细胞和 T 淋巴细胞共同培养的体外模型,使用维甲酸受体的激动剂和拮抗剂来抑制/刺激 Sertoli 细胞中的维甲酸信号转导:结果:我们的研究结果表明,9cRA 能抑制 Sertoli 细胞和淋巴细胞中免疫抑制基因的表达,增强促炎因子的表达,提高淋巴细胞的活力,降低细胞凋亡率。此外,我们还发现 9cRA 可通过 RAR 和 RXR 阻断淋巴细胞凋亡,抑制 FasL/Fas/Caspase 8 和 Bax/Bcl-2/Caspase 9 通路。最后,我们还发现 9cRA 信号在 Sertoli 细胞中可抑制 Treg 分化:总之,我们的研究结果表明,视黄醇信号负向调节 Sertoli 细胞的免疫特权功能,这对确保男性生育能力至关重要。9cRA抑制淋巴细胞凋亡,这可能与自身免疫、炎症以及不育的发展有关。
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来源期刊
Reproductive Biology and Endocrinology
Reproductive Biology and Endocrinology 医学-内分泌学与代谢
CiteScore
7.90
自引率
2.30%
发文量
161
审稿时长
4-8 weeks
期刊介绍: Reproductive Biology and Endocrinology publishes and disseminates high-quality results from excellent research in the reproductive sciences. The journal publishes on topics covering gametogenesis, fertilization, early embryonic development, embryo-uterus interaction, reproductive development, pregnancy, uterine biology, endocrinology of reproduction, control of reproduction, reproductive immunology, neuroendocrinology, and veterinary and human reproductive medicine, including all vertebrate species.
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