Defective gp130-mediated signal transducer and activator of transcription (STAT) signaling results in degenerative joint disease, gastrointestinal ulceration, and failure of uterine implantation

Ernst, M; Inglese, M; Waring, P; Campbell, IK; Bao, SS; Clay, FJ; Alexander, WS; Wicks, IP; Tarlinton, DM; Novak, U; Heath, JK; Dunn, AR

Author(s): Ernst, M; Inglese, M; Waring, P; Campbell, IK; Bao, SS; Clay, FJ; Alexander, WS; Wicks, IP; Tarlinton, DM; Novak, U; Heath, JK; Dunn, AR;
Details: Publication Year 2001-07-16,Volume 194,Issue #2,Page 189-203
Journal Title: JOURNAL OF EXPERIMENTAL MEDICINE
Publication Type: Journal Article
Abstract: The receptor subunit gp130 transduces multiple cell type-specific activities of the leukemia inhibitory factor (LIF)interleukin (IL)-6 family of cytokines through the signal transducer and activator of transcription (STAT) and src homology 2 domain-bearing protein tyrosine phosphatase (SHP)-2/ras/Erk pathways. To define STAT-dependent physiological responses, we generated mice with a COOH-terminal gp130(Delta STAT) "knock-in" mutation which deleted all STAT-binding sites, gp130(Delta STAT) mice phenocopyed mice deficient for IL-6 (impaired humoral and mucosal immune and hepatic acute phase responses) and LIF (failure of blastocyst implantation). However, unlike mice with null mutations in any of the components in the gp130 signaling pathway, gp130(Delta STAT) mice also displayed gastrointestinal ulceration and a severe joint disease with features of chronic synovitis, cartilaginous metaplasia, and degradation of the articular cartilage. Mitogenic hyperresponsiveness of synovial cells to the LIF/IL-6 family of cytokines was caused by sustained gp130-mediated SHP-2/ras/Erk activation due to impaired STAT-mediated induction of suppressor of cytokine signaling (SOCS) proteins which normally limits gp130 signaling. Therefore, the joint pathology in gp130(Delta STAT) mice is likely to arise from the disturbance of the otherwise balanced activation of the SHP-2/ras/Erk and STAT signaling cascades emanating from gp130.
Publisher: ROCKEFELLER UNIV PRESS
Keywords: LEUKEMIA INHIBITORY FACTOR; STIMULATING FACTOR-RECEPTOR; TRANSGENIC MICE; IL-6 RECEPTOR; INTERLEUKIN-6 FAMILY; TARGETED DISRUPTION; CYTOKINE RECEPTORS; STEM-CELLS; IN-VIVO; GP130
Publisher's Version: https://doi.org/10.1084/jem.194.2.189
Terms of Use/Rights Notice: Refer to copyright notice on published article.

Creation Date: 2001-07-16 12:00:00