國家衛生研究院 NHRI:Item 3990099045/11392
English  |  正體中文  |  简体中文  |  Items with full text/Total items : 12340/13512 (91%)
Visitors : 2256985      Online Users : 296
RC Version 6.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
Scope Tips:
  • please add "double quotation mark" for query phrases to get precise results
  • please goto advance search for comprehansive author search
    •  Adv. Search
    Home ‧ Login ‧ Upload ‧ Help ‧ About ‧ Administer Goto mobile version
    NHRI > Immunology Research Center > Yu-Wen Su > Periodical Articles >  Item 3990099045/11392


    Please use this identifier to cite or link to this item: http://ir.nhri.org.tw/handle/3990099045/11392


    Title: PP4 deficiency leads to DNA replication stress that impairs immunoglobulin class switch efficiency
    Authors: Chen, MY;Hsu, WC;Hsu, SC;Yang, YS;Chuang, TH;Lin, WJ;Tan, TH;Su, YW
    Contributors: Immunology Research Center;National Institute of Infectious Diseases and Vaccinology
    Abstract: The serine/threonine phosphatase PP4 has been implicated in DNA damage repair and cell cycle regulation through its dephosphorylation of specific substrates. We previously showed that PP4 is required for mouse B cell development, germinal center (GC) formation and immunoglobulin (Ig) class switch recombination (CSR). Here, we investigate the mechanisms underlying this requirement and demonstrate that murine PP4-deficient B lymphocytes have a defect in cell proliferation. Strikingly, the DNA damage response pathway that involves ATM/p53 and is linked to cell cycle arrest and impaired cell survival is strongly induced in these mutant B cells. In response to LPS + IL-4, stimuli that trigger IgG1 production, these PP4-deficient B cells show inefficient phosphorylation of ATR, leading to reduced retention of γH2AX-NBS1 complexes at sites of DNA damage, and compromised switching to IgG1. However, beyond the cell proliferation phase, conditional deletion of PP4 under the control of AID/cre completely restores normal IgG1 production in mutant B cell cultures. In vivo, co-deletion of PP4 and p53 by AID/cre partially rescues switching to IgG1 in B cells of mice immunized with TNP-KLH. Our findings establish that PP4 is indispensable for preventing DNA replication stress that could interfere with CSR, thereby promoting antibody switching during the humoral immune response.
    Date: 2019-07
    Relation: Cell Death and Differentiation. 2019 Jul;26 (7):1221-1234.
    Link to: http://dx.doi.org/10.1038/s41418-018-0199-z
    JIF/Ranking 2023: http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=NHRI&SrcApp=NHRI_IR&KeyISSN=1350-9047&DestApp=IC2JCR
    Cited Times(WOS): https://www.webofscience.com/wos/woscc/full-record/WOS:000470970300004
    Cited Times(Scopus): https://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85053546624
    Appears in Collections:[Yu-Wen Su] Periodical Articles
    [Tse-Hua Tan] Periodical Articles
    [Wen-Jye Lin] Periodical Articles
    [Tsung-Hsien Chuang] Periodical Articles
    [Shu-Ching Hsu] Periodical Articles

    Files in This Item:

    File Description SizeFormat
    SCP85053546624.pdf3584KbAdobe PDF278View/Open


    All items in NHRI are protected by copyright, with all rights reserved.

    Related Items in TAIR

    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - Feedback