Biol Res. 2024 Sep 9;57(1):64.doi: 10.1186/s40659-024-00544-8.

中文速读

本研究证明小鼠睾丸巨噬细胞能自主合成睾酮,并受Cebpb调控。使用Entranster-H4000转染试剂将Cebpb过表达质粒转染至原代睾丸巨噬细胞,通过qPCR、免疫荧光和CUT-RUN等方法验证了Cebpb对睾酮合成关键酶的调控作用。

小鼠生殖质粒DNAprimary testicular macrophages

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Mouse testicular macrophages can independently produce testosterone and are regulated by Cebpb

Affiliations

Affiliations

  • 1 Department of Urology, The Second Affiliated Hospital of Soochow University, NO.1055 SanXiang Road, Suzhou, Jiangsu Province, 215000, China.
  • 2 State Key Laboratory of Radiation Medicine and Protection, School of Radiation Medicine and Protection, Medical College of Soochow University, Suzhou, China.
  • 3 State Key Laboratory of Radiation Medicine and Protection, School of Radiation Medicine and Protection, Medical College of Soochow University, Suzhou, China. cuifengmei@suda.edu.cn.
  • 4 State Key Laboratory of Radiation Medicine and Protection, School of Radiation Medicine and Protection, Medical College of Soochow University, Suzhou, China. happyqiu@suda.edu.cn.
  • 5 Department of Urology, The Second Affiliated Hospital of Soochow University, NO.1055 SanXiang Road, Suzhou, Jiangsu Province, 215000, China. xueboxin1992@suda.edu.cn.
  • 6 Department of Urology, The Second Affiliated Hospital of Soochow University, NO.1055 SanXiang Road, Suzhou, Jiangsu Province, 215000, China. liuxiaolong2005@suda.edu.cn.

Abstract

Background: Testicular macrophages (TM) have long been recognized for their role in immune response within the testicular environment. However, their involvement in steroid hormone synthesis, particularly testosterone, has not been fully elucidated. This study aims to explore the capability of TM to synthesize and secrete testosterone de novo and to investigate the regulatory mechanisms involved.

Results: Transcriptomic analysis revealed significant expression of Cyp11a1, Cyp17a1, Hsd3b1, and Hsd17b3 in TM, which are key enzymes in the testosterone synthesis pathway. qPCR analysis and immunofluorescence validation confirmed the autonomous capability of TM to synthesize testosterone. Ablation of TM in mice resulted in decreased physiological testosterone levels, underscoring the significance of TM in maintaining testicular testosterone levels. Additionally, the study also demonstrated that Cebpb regulates the expression of these crucial genes, thereby modulating testosterone synthesis.

Conclusions: This research establishes that TM possess the autonomous capacity to synthesize and secrete testosterone, contributing significantly to testicular testosterone levels. The transcription factor Cebpb plays a crucial role in this process by regulating the expression of key genes involved in testosterone synthesis.

Keywords: Cebpb; De novo synthesis; Testicular macrophage; Testosterone.

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