Thymosin-β4: A key modifier of renal disease

被引:14
作者
Vasilopoulou, Elisavet [1 ,2 ]
Riley, Paul R. [3 ]
Long, David A. [2 ]
机构
[1] Univ Kent, Medway Sch Pharm, Anson Bldg,Cent Ave, Chatham ME4 4TB, Kent, England
[2] UCL Inst Child Hlth, Dev Biol & Canc Programme, London, England
[3] Univ Oxford, Dept Physiol Anat & Genet, Oxford, England
基金
英国医学研究理事会;
关键词
Ac-SDKP; cytoskeleton; fibrosis; glomerulus; inflammation; kidney disease; podocyte; thymosin-4; ASPARTYL-LYSYL-PROLINE; CHRONIC KIDNEY-DISEASE; PEPTIDE AC-SDKP; CELL-MIGRATION; PROLYL OLIGOPEPTIDASE; ACTIN POLYMERIZATION; CONVERTING-ENZYME; MOUSE MODEL; BETA-4; FIBROSIS;
D O I
10.1080/14712598.2018.1473371
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Introduction: There is an urgent need for new treatments for chronic kidney disease (CKD). Thymosin-4 is a peptide that reduces inflammation and fibrosis and has the potential to restore endothelial and epithelial cell injury, biological processes involved in the pathophysiology of CKD. Therefore, thymosin-4 could be a novel therapeutic direction for CKD.Areas covered: Here, we review the current evidence on the actions of thymosin-4 in the kidney in health and disease. Using transgenic mice, two recent studies have demonstrated that endogenous thymosin-4 is dispensable for healthy kidneys. In contrast, lack of endogenous thymosin-4 exacerbates mouse models of glomerular disease and angiotensin-II-induced renal injury. Administration of exogenous thymosin-4, or its metabolite, Ac-SDKP, has shown therapeutic benefits in a range of experimental models of kidney disease.Expert opinion: The studies conducted so far reveal a protective role for thymosin-4 in the kidney and have shown promising results for the therapeutic potential of exogenous thymosin-4 in CKD. Further studies should explore the mechanisms by which thymosin-4 modulates kidney function in different types of CKD. Ac-SDKP treatment has beneficial effects in many experimental models of kidney disease, thus supporting its potential use as a new treatment strategy.
引用
收藏
页码:185 / 192
页数:8
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