Department of Histology and Cell Biology, Faculty of Medicine, Benha University, Benha, Egypt.
Department of Anatomy, Faculty of Medicine, Umm Al Qura University, Mecca, Saudi Arabia.
Life Sci. 2021 Apr 1;270:119122. doi: 10.1016/j.lfs.2021.119122. Epub 2021 Jan 26.
The adrenal glands have striking morpho-biochemical features that render them vulnerable to the effects of toxins.
This study was conducted to explore the therapeutic utility of extracellular vesicles derived from bone marrow mesenchymal stem cells (BMSC-EVs) against fluoride-induced adrenal toxicity.
The work included isolation and further identification of BMSC-EVs by transmission electron microscopy and flow cytometric analysis. Adrenal toxicity in rats was induced by oral administration of 300 ppm of sodium fluoride (NaF) in drinking water for 60 days followed by a single dose injection of BMSC-EVs. The effects of BMSC-EVs against NaF was evaluated by adrenal oxidant/antioxidant biomarkers, hormonal assay of plasma adrenocorticotrophic hormone (ACTH) and corticosterone (CORT) and mRNA gene expression quantitation for adrenal cortical steroidogenic pathway-encoding genes. Histopathological examination of the adrenal tissue was performed.
BMSC-EVs were effectively isolated and characterized. NaF exposure decreased adrenal superoxide dismutase and catalase activities, increased adrenal malondialdehyde levels, elevated plasma ACTH, diminished CORT concentrations and downregulated the adrenal cortical steroidogenic pathway-encoding genes. In addition, NaF-induced marked adrenal histopathological lesions.
BMSC-EVs treatment repaired damaged adrenal tissue and recovered its function greatly following NaF consumption. BMSC-EVs reversed the toxic effects of NaF and reprogramed injured adrenal cells by activating regenerative processes.
肾上腺具有显著的形态生化特征,使其容易受到毒素的影响。
本研究旨在探讨骨髓间充质干细胞衍生的细胞外囊泡(BMSC-EVs)治疗氟化物诱导的肾上腺毒性的治疗效果。
通过透射电子显微镜和流式细胞术分析,对 BMSC-EVs 进行分离和进一步鉴定。通过在饮用水中口服 300ppm 的氟化钠(NaF)60 天,然后单次注射 BMSC-EVs,诱导大鼠肾上腺毒性。通过肾上腺氧化应激/抗氧化生物标志物、血浆促肾上腺皮质激素(ACTH)和皮质酮(CORT)的激素测定以及肾上腺皮质甾体生成途径编码基因的 mRNA 基因表达定量,评估 BMSC-EVs 对 NaF 的作用。对肾上腺组织进行组织病理学检查。
成功分离和鉴定了 BMSC-EVs。NaF 暴露降低了肾上腺超氧化物歧化酶和过氧化氢酶的活性,增加了肾上腺丙二醛水平,升高了血浆 ACTH,降低了 CORT 浓度,并下调了肾上腺皮质甾体生成途径编码基因。此外,NaF 诱导了明显的肾上腺组织病理学损伤。
BMSC-EVs 治疗可修复 NaF 消耗后受损的肾上腺组织并极大地恢复其功能。BMSC-EVs 通过激活再生过程,逆转了 NaF 的毒性作用,并重新编程了受损的肾上腺细胞。