WAN-TSENG HSUHuang W.-J.BOR-LUEN CHIANGPING-HUEI TSENG2021-07-022021-07-0220211465-3249https://www.scopus.com/inward/record.uri?eid=2-s2.0-85104367771&doi=10.1016%2fj.jcyt.2021.01.007&partnerID=40&md5=3e5421a4e5ddb52aa4b19c505b5db9d0https://scholars.lib.ntu.edu.tw/handle/123456789/567706Background aims: Adipose-derived stem cells (ASCs) offer promising therapeutic possibilities for immunomodulation. Butyrate (BA) exerts potent anti-inflammatory effects and exhibits multiple regulatory functionalities in adipose tissue (AT). The authors a[SDGs]SDG3amphiregulin; butyric acid; gamma interferon; histone H3; inducible nitric oxide synthase; interleukin 10; nitric oxide; nitric oxide synthase; transcription factor FOXP3; tumor necrosis factor; butyric acid derivative; adipose derived stem cell; animal cButyrate modulates adipose-derived stem cells isolated from polygenic obese and diabetic mice to drive enhanced immunosuppressionjournal article10.1016/j.jcyt.2021.01.007338753842-s2.0-85104367771