Hutchison Jennifer C, Trim Paul J, Whiley Penny A F, Handelsman David J, Snel Marten F, Groome Nigel P, Hedger Mark P, Loveland Kate L
Centre for Reproductive Health, Hudson Institute of Medical Research, Clayton, VIC 3168, Australia.
Department of Molecular and Translational Science, Monash University, Clayton, VIC 3168, Australia.
Endocrinology. 2025 Mar 24;166(5). doi: 10.1210/endocr/bqaf054.
Bioactivity of the hormone and growth factor activin A is central to fertility and health. Dysregulated circulating activin levels occur with medication usage and multiple pathological conditions. The inhibin-alpha knockout mouse (InhaKO) models chronic activin elevation and unopposed activin A bioactivity. In InhaKO fetal testes, lipid droplet, steroid profiles, and seminiferous cords are abnormal; adults develop gonadal and adrenal tumors due to chronic activin A excess exposure. Here we address how this exposure affects lipid, metabolite, and steroid composition in whole testes, ovaries, and adrenals of adult InhaKO mice using histological, transcriptomic, and mass spectrometry (MS) methods, including MS imaging (matrix-assisted laser desorption/ionization-MS imaging). Matrix-assisted laser desorption/ionization-MS imaging delineated spatial lipid profiles within interstitial, inner cord, and outer cord regions containing normal spermatogenesis; these differed between wild-type and KO samples. In proximity to tumors, lipids showed distinctive distribution patterns both within and adjacent to the tumor. Significantly altered lipids and metabolic profiles in whole InhaKO testes homogenates were linked to energy-related pathways. In gonads and adrenal glands of both sexes, steroidogenic enzyme transcription, and steroids are different, as expected. Lipid profiles and steroidogenic enzyme proteins, HSD3B1 and CYP11A1, are affected within and near gonadal tumors. This documents organ-specific effects of chronic activin A elevation on lipid composition and cellular metabolism, in both histologically normal and tumor-affected areas. The potential for activin A to influence numerous steroidogenic processes should be considered in context and with spatial precision, particularly in relationship to pathologies.
激素和生长因子激活素A的生物活性对生育能力和健康至关重要。循环中激活素水平失调会伴随药物使用和多种病理状况出现。抑制素α基因敲除小鼠(InhaKO)模拟了慢性激活素升高和激活素A生物活性不受拮抗的情况。在InhaKO胎儿睾丸中,脂滴、类固醇谱和生精小管均异常;成年小鼠由于长期暴露于过量的激活素A而发生性腺和肾上腺肿瘤。在此,我们使用组织学、转录组学和质谱(MS)方法,包括MS成像(基质辅助激光解吸/电离-MS成像),研究这种暴露如何影响成年InhaKO小鼠全睾丸、卵巢和肾上腺中的脂质、代谢物和类固醇组成。基质辅助激光解吸/电离-MS成像描绘了含有正常精子发生的间质、内小管和外小管区域内的空间脂质谱;这些在野生型和基因敲除样本之间存在差异。在肿瘤附近,脂质在肿瘤内部和相邻区域均呈现出独特的分布模式。InhaKO全睾丸匀浆中显著改变的脂质和代谢谱与能量相关途径有关。正如预期的那样,在两性的性腺和肾上腺中,类固醇生成酶转录和类固醇均有所不同。性腺肿瘤内部和附近的脂质谱以及类固醇生成酶蛋白HSD3B1和CYP11A1均受到影响。这证明了慢性激活素A升高对组织学正常和肿瘤影响区域的脂质组成和细胞代谢具有器官特异性作用。在考虑激活素A影响众多类固醇生成过程的可能性时,应结合具体情况并精确到空间位置,尤其是与病理学的关系。