@article{cfed8bb560aa40239184aa6a80dfd9cb,
title = "Socs, Spred, And Nr4a: Negative Regulators Of Cytokine Signaling And Transcription In Immune Tolerance",
abstract = "Cytokines are important intercellular communication tools for immunity. Most cytokines utilize the JAK-STAT and Ras-ERK pathways to promote gene transcription and proliferation; however, this signaling is tightly regulated. The suppressor of cytokine signaling (SOCS) family and Spred family are a representative negative regulators of the JAK-STAT pathway and the Ras-ERK pathway, respectively. The SOCS family regulates the differentiation and function of CD4+T cells, CD8+T cells, and regulatory T cells, and is involved in immune tolerance, anergy, and exhaustion. Spred family proteins have been shown to inactivate Ras by recruiting the Ras-GTPase neurofibromatosis type 1 (NF1) protein. Human genetic analysis has shown that SOCS family members are strongly associated with autoimmune diseases, allergies, and tumorigenesis, and SPRED1 is involved in NF1-like syndromes and tumors. We also identified the NR4a family of nuclear receptors as a key transcription factor for immune tolerance that suppresses cytokine expression and induces various immuno-regulatory molecules including SOCS1.",
keywords = "anergy, autoimmunity, cytokine signal, immune tolerance, regulatory T cells",
author = "Akihiko Yoshimura and Daisuke Aki and Minako Ito",
note = "Funding Information: We would like to thank Mari Ikeda, Yasuko Hirata, and Yukiko Tokifuji (Keio University) for their technical assistance. This work was supported by JSPS KAKENHI (S) JP17H06175, 17K15667, 19H04817, and 19K16618, AMED-CREST JP 20gm1110009 grants, AMED-PRIME 20gm6210012, Princess Takamatsu Cancer Research Found and Yasuda Medical Foundation, the Kishimoto Foun- dation, the Tomizawa Jun-ichi & Keiko Fund of Molecular Biology Society of Japan for Young Scientist, The Mitsubishi Foundation, the Mochida Memorial Foundation for Medical and Pharmaceutical Research, the Takeda Science Foundation, the Uehara Memorial Foundation, the Naito Memorial Foundation, the Kanae Foundation, the SENSHIN Medical Research Foundation, the Astellas Foundation for Research on Metabolic Disorders, an Inoue Research Award, a Life Science Research Award, and Keio Gijuku Academic Developmental Funds. Funding Information: We would like to thank Mari Ikeda, Yasuko Hirata, and Yukiko Tokifuji (Keio University) for their technical assistance. This work was supported by JSPS KAKENHI (S) JP17H06175, 17K15667, 19H04817, and 19K16618, AMED-CREST JP 20gm1110009 grants, AMED-PRIME 20gm6210012, Princess Takamatsu Cancer Research Found and Yasuda Medical Foundation, the Kishimoto Foun-dation, the Tomizawa Jun-ichi & Keiko Fund of Molecular Biology Society of Japan for Young Scientist, The Mitsubishi Foundation, the Mochida Memorial Foundation for Medical and Pharmaceutical Research, the Takeda Science Foundation, the Uehara Memorial Foundation, the Naito Memorial Foundation, the Kanae Foundation, the SENSHIN Medical Research Foundation, the Astellas Foundation for Research on Metabolic Disorders, an Inoue Research Award, a Life Science Research Award, and Keio Gijuku Academic Developmental Funds. Publisher Copyright: {\textcopyright}2021 The Japan Academy",
year = "2021",
doi = "10.2183/pjab.97.016",
language = "English",
volume = "97",
pages = "277--291",
journal = "Proceedings of the Japan Academy Series B: Physical and Biological Sciences",
issn = "0386-2208",
publisher = "Japan Academy",
number = "6",
}