| Literature DB >> 28190773 |
Jinxiu Rui1, Songyan Deng1, Arnon Arazi2, Ana Luisa Perdigoto3, Zongzhi Liu4, Kevan C Herold5.
Abstract
Type 1 diabetes (T1D) is a chronic autoimmune disease that involves immune-mediated destruction of β cells. How β cells respond to immune attack is unknown. We identified a population of β cells during the progression of T1D in non-obese diabetic (NOD) mice that survives immune attack. This population develops from normal β cells confronted with islet infiltrates. Pathways involving cell movement, growth and proliferation, immune responses, and cell death and survival are activated in these cells. There is reduced expression of β cell identity genes and diabetes antigens and increased immune inhibitory markers and stemness genes. This new subpopulation is resistant to killing when diabetes is precipitated with cyclophosphamide. Human β cells show similar changes when cultured with immune cells. These changes may account for the chronicity of the disease and the long-term survival of β cells in some patients.Entities:
Keywords: autoimmunity; immune regulation; stem cell; β cell
Mesh:
Substances:
Year: 2017 PMID: 28190773 PMCID: PMC5342930 DOI: 10.1016/j.cmet.2017.01.005
Source DB: PubMed Journal: Cell Metab ISSN: 1550-4131 Impact factor: 27.287