Beta-cell function and human islet transplantation: can we improve?

被引:10
|
作者
Chen, Jennifer [1 ]
Gunton, Jenny E. [1 ,2 ,3 ,4 ]
机构
[1] Univ Sydney, Westmead Inst Med Res, Westmead Hosp, Sydney, NSW, Australia
[2] Westmead Hosp, Dept Endocrinol & Diabet, Sydney, NSW, Australia
[3] Garvan Inst Med Res, Sydney, NSW, Australia
[4] Univ New South Wales, St Vincents Clin Sch, Sydney, NSW, Australia
基金
澳大利亚国家健康与医学研究理事会;
关键词
beta-cells; islet transplantation; human; diabetes; HUMAN PANCREATIC-ISLETS; INSULIN-SECRETION; ALPHA-CELLS; ENDOCRINE PANCREAS; BASEMENT-MEMBRANE; FACTOR EXPRESSION; CULTURED ISLETS; GENE-EXPRESSION; BLOOD-FLOW; SHORT-TERM;
D O I
10.1530/JOE-20-0590
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Islet transplantation, a therapeutic option to treat type 1 diabetes, is not yet as successful as whole-pancreas transplantation as a treatment for diabetes. Mouse models are commonly used for islet research. However, it is clear disparities exist between islet transplantation outcomes in mice and humans. Given the shortage of transplant-grade islets, it is crucial that we further our understanding of factors that determine long-term islet survival and function post-transplantation. In turn, this may lead to new therapeutic targets and strategies that will improve transplant outcomes. Here, we summarise the current landscape in clinical transplantation, highlight underlying similarities and differences between mouse and human islets, and review intervent ions that are being considered to create a new pool of beta-cells for clinical application.
引用
收藏
页码:R99 / R112
页数:14
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