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脂肪源性干细胞及其细胞外囊泡在 3 型心肾综合征实验模型中的分子和细胞机制:组织学和生化研究。

Molecular and Cellular Mechanisms Involved in Adipose-derived stem cell and their extracellular vesicles in an Experimental Model of Cardio- renal Syndrome type 3: Histological and Biochemical Study.

机构信息

Department of Anatomy, Faculty of Medicine, Umm Al-Qura University, Saudi Arabia.

Department of Histology, Faculty of Medicine, Suez Canal University, Ismailia, Egypt.

出版信息

Tissue Cell. 2022 Aug;77:101842. doi: 10.1016/j.tice.2022.101842. Epub 2022 Jun 7.

Abstract

A cardio-renal syndrome (CRS) is a medical condition in which kidney problems are accompanied by heart problems and diagnosed when acute kidney injury contributes to the development of acute cardiac injury. Regenerative medicine is becoming increasingly interested in adipose stem cells. We evaluated the effect of both adipose-derived stem cell extracellular vesicles (ADSCs-EVs) and adipose stem cells (ADSCs) on an experimental model of CRSIII. In this study, isolation, and further identification of ADSCs and ADSCs-EVs by transmission electron microscopy and flow cytometric analysis. Cardio-renal syndrome in rats was induced by renal artery ligation RAL followed by a single dose injection of both ADSCs and ADSCs-EVs in separate groups. The effects of ADSCs-EVs and ADSCs against induced CRSIII were evaluated by both renal and cardiac oxidant/antioxidant biomarkers, renal function, and mRNA gene expression quantitation for atrial natriuretic peptide (ANP), p300, and myocyte enhancer factor 2 (MEF2C and MEF2A), as well as myocardin (MYOCD), as molecules associated with cardiac hypertrophy. Additionally, histological and immunohistochemical studies of cardiac and renal tissues were done. ADSCs-EVs were effectively isolated and characterized. ADSCs-EVs and ADSCs reversed induced CRSIII, evidenced by considerably decreased serum urea and creatinine levels. Returned oxidant/antioxidant stability, and decreased caspase 3-mediated apoptotic programmed cell death in cardiac and renal tissues. Additionally, they led to successful down-regulation of hypertrophic cardiac genes levels and reversed histopathological cardiac and renal injures. ADSCs-derived extracellular vesicles and ADSCs injection restored damaged cardiac and renal tissue and improved its function greatly following induced CRSIII. They could therefore be useful as a means of protecting the heart from the deleterious effects of acute renal injury and reprogramed injured cardiac cells by activating regenerative processes. SIMPLE SUMMARY: Cardiorenal syndrome (CRS) type III is a subcategory of CRS whereby acute kidney injury (AKI) could contribute to the development of acute cardiac dysfunction. This study provided innovatory data regarding the role of adipose-derived stem cell extracellular vesicles ADSCs-EVs and adipose stem cells (ADSCs) in acute renal and cardiac dysfunction and renal biopsy specimens in the form of interstitial inflammation/tubular degeneration. The main cause of renal and cardiac dysfunction is identified to be the activation and accumulation of inflammatory cells and oxidants in the interstitium, surrounded by increased amounts of extracellular matrix, and ADSCs-EVs have been proposed as a contributor factor. The study has evidenced that both ADSCs-EVs and adipose stem cells display beneficial effects on renal and cardiac tissues survival in terms of the frequent occurrence of cardio-renal syndrome, ADSC-EVs treatment repaired damaged renal and cardiac tissues and recovered their function. ADSC-EVs reversed the effects of cardio-renal syndrome and reprogramed injured cells by activating regenerative processes. The clinical significance of the results presented in future studies needs to be investigated further.

摘要

心肾综合征(CRS)是一种肾脏问题伴有心脏问题的医学病症,当急性肾损伤导致急性心脏损伤时即可诊断。再生医学越来越关注脂肪干细胞。我们评估了脂肪来源干细胞细胞外囊泡(ADSCs-EVs)和脂肪干细胞(ADSCs)对 CRSIII 实验模型的影响。在这项研究中,通过透射电子显微镜和流式细胞术分析对 ADSCs 和 ADSCs-EVs 进行了分离和进一步鉴定。通过单侧肾动脉结扎(RAL)诱导大鼠心肾综合征,然后在不同组中单次注射 ADSCs 和 ADSCs-EVs。通过肾脏和心脏氧化/抗氧化生物标志物、肾功能以及心房利钠肽(ANP)、p300 和肌细胞增强因子 2(MEF2C 和 MEF2A)的 mRNA 基因表达定量,评估 ADSCs-EVs 和 ADSCs 对诱导的 CRSIII 的作用,以及心肌营养素(MYOCD),作为与心脏肥大相关的分子。此外,还对心脏和肾脏组织进行了组织学和免疫组织化学研究。有效地分离和鉴定了 ADSCs-EVs。ADSCs-EVs 和 ADSCs 逆转了诱导的 CRSIII,血清尿素和肌酐水平明显降低。心脏和肾脏组织中氧化/抗氧化稳定性恢复,caspase 3 介导的凋亡程序性细胞死亡减少。此外,它们导致心脏肥大基因水平的成功下调,并逆转了心脏和肾脏的组织损伤。ADSCs 衍生的细胞外囊泡和 ADSCs 注射在诱导 CRSIII 后,可恢复受损的心脏和肾脏组织,并大大改善其功能。因此,它们可作为一种保护心脏免受急性肾损伤有害影响的手段,并通过激活再生过程来重新编程受损的心脏细胞。简单总结:心肾综合征(CRS)III 型是 CRS 的一个亚类,急性肾损伤(AKI)可能导致急性心功能障碍。本研究提供了关于脂肪来源干细胞细胞外囊泡 ADSCs-EVs 和脂肪干细胞(ADSCs)在急性肾和心脏功能障碍以及肾脏活检标本中(以间质炎症/肾小管变性的形式)的作用的创新性数据。肾和心脏功能障碍的主要原因被确定为间质中炎症细胞和氧化剂的激活和积累,周围有大量细胞外基质,并且 ADSCs-EVs 被提出为一个贡献因素。研究表明,ADSCs-EVs 和脂肪干细胞在经常发生的心肾综合征的情况下对肾脏和心脏组织的存活具有有益作用,ADSC-EVs 治疗修复了受损的肾脏和心脏组织并恢复了其功能。ADSCs-EVs 通过激活再生过程逆转了心肾综合征的作用并重新编程了受损细胞。需要进一步研究未来研究中呈现的结果的临床意义。

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