作者
Irène Cimino,Hanna Kim,Y. C. Loraine Tung,Kent Pedersen,Debra Rimmington,John A. Tadross,Sara Kohnke,Ana Neves‐Costa,André Barros,Stephanie Joaquim,D Bennett,Audrey Melvin,Sam Lockhart,Anthony Rostron,Jon Scott,Hui Liu,Keith Burling,Peter Barker,Menna R. Clatworthy,E-Chiang Lee,A. John Simpson,Giles S.H. Yeo,Luís F. Moita,Kendra K. Bence,Sebastian B. Jørgensen,Anthony P. Coll,Danna M. Breen,Stephen O’Rahilly
摘要
Significance GDF15, a hormone produced by a wide variety of cells undergoing different types of stress, acts on a receptor in the brain where it transmits signals that are perceived by the organism as aversive. We now report an action of GDF15, whereby it activates the endocrine stress response and increases circulating levels of the principal glucocorticoid (a “stress” steroid). By studying mice genetically deficient in GDF15, we also demonstrate that GDF15 is a key signal through which damage due to toxic chemicals activates the steroid stress response. GDF15 is currently being explored as an antiobesity drug and examination of the degree and duration of the steroid effect will need to be incorporated into any human trials.