Impact of Excess Activin A on the Lipids, Metabolites, and Steroids of Adult Mouse Reproductive Organs.

IF 3.8 3区 医学 Q2 ENDOCRINOLOGY & METABOLISM
Jennifer C Hutchison, Paul J Trim, Penny A F Whiley, David J Handelsman, Marten F Snel, Nigel P Groome, Mark P Hedger, Kate L Loveland
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Abstract

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.

过量激活素A对成年小鼠生殖器官脂质、代谢物和类固醇的影响。
激素和生长因子激活素A的生物活性对生育和健康至关重要。循环激活素水平失调发生在药物使用和多种病理条件下。抑制素α敲除小鼠(InhaKO)模拟慢性激活素升高和无对抗激活素A的生物活性。在InhaKO胎儿睾丸中,脂滴、类固醇谱和精索异常;成人由于长期过量接触激活素A而产生性腺和肾上腺肿瘤。在这里,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小鼠整个睾丸、卵巢和肾上腺中的脂质、代谢物和类固醇成分。基质辅助激光解吸/电离-质谱成像描绘了含有正常精子发生的间质、内索和外索区域的空间脂质谱;这些在野生型和KO样本之间有所不同。在肿瘤附近,脂质在肿瘤内和肿瘤附近均表现出独特的分布模式。整个InhaKO睾丸匀浆中脂质和代谢谱的显著改变与能量相关途径有关。正如预期的那样,在两性性腺和肾上腺中,类固醇生成酶转录和类固醇是不同的。脂质谱和甾体原酶蛋白HSD3B1和CYP11A1在性腺肿瘤内部和附近受到影响。本研究记录了在组织学正常和肿瘤影响区域,慢性激活素A升高对脂质组成和细胞代谢的器官特异性影响。激活素A影响许多甾体生成过程的可能性应在背景和空间精确的情况下考虑,特别是与病理学的关系。
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来源期刊
Endocrinology
Endocrinology 医学-内分泌学与代谢
CiteScore
8.10
自引率
4.20%
发文量
195
审稿时长
2-3 weeks
期刊介绍: The mission of Endocrinology is to be the authoritative source of emerging hormone science and to disseminate that new knowledge to scientists, clinicians, and the public in a way that will enable "hormone science to health." Endocrinology welcomes the submission of original research investigating endocrine systems and diseases at all levels of biological organization, incorporating molecular mechanistic studies, such as hormone-receptor interactions, in all areas of endocrinology, as well as cross-disciplinary and integrative studies. The editors of Endocrinology encourage the submission of research in emerging areas not traditionally recognized as endocrinology or metabolism in addition to the following traditionally recognized fields: Adrenal; Bone Health and Osteoporosis; Cardiovascular Endocrinology; Diabetes; Endocrine-Disrupting Chemicals; Endocrine Neoplasia and Cancer; Growth; Neuroendocrinology; Nuclear Receptors and Their Ligands; Obesity; Reproductive Endocrinology; Signaling Pathways; and Thyroid.
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