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B Cell-Intrinsic and-Extrinsic Regulation of Antibody Responses by PARP14,an Intracellular(ADP-Ribosyl)Transferase

Authors
 Sung Hoon Cho  ;  Ariel Raybuck  ;  Mei Wei  ;  John Erickson  ;  Ki Taek Nam  ;  Reagan G. Cox  ;  Alyssa Trochtenberg  ;  James W. Thomas  ;  John Williams  ;  Mark Boothby 
Citation
 JOURNAL OF IMMUNOLOGY, Vol.191(16) : 3169-3178, 2014 
Journal Title
 JOURNAL OF IMMUNOLOGY 
ISSN
 0022-1767 
Issue Date
2014
MeSH
Adaptive Immunity/immunology* ; Animals ; Antibody Formation/immunology* ; B-Lymphocytes/immunology* ; Cell Differentiation/immunology ; Immunity, Humoral/immunology* ; Immunoglobulin A/immunology ; Mice ; Mice, Inbred C57BL ; Mice, Knockout ; Mice, Transgenic ; Poly(ADP-ribose) Polymerases/immunology* ; T-Lymphocytes, Helper-Inducer/cytology ; T-Lymphocytes, Helper-Inducer/immunology
Abstract
The capacity to achieve sufficient concentrations of Ag-specific Ab of the appropriate isotypes is a critical component of immunity that requires efficient differentiation and interactions of Ag-specific B and Th cells along with dendritic cells. Numerous bacterial toxins catalyze mono(ADP-ribosyl)ation of mammalian proteins to influence cell physiology and adaptive immunity. However, little is known about biological functions of intracellular mammalian mono(ADP-ribosyl)transferases, such as any ability to regulate Ab responses. poly-(ADP-ribose) polymerase 14 (PARP14), an intracellular protein highly expressed in lymphoid cells, binds to STAT6 and encodes a catalytic domain with mammalian mono(ADP-ribosyl)transferase activity. In this article, we show that recall IgA as well as the STAT6-dependent IgE Ab responses are impaired in PARP14-deficient mice. Whereas PARP14 regulation of IgE involved a B cell-intrinsic process, the predominant impact on IgA was B cell extrinsic. Of note, PARP14 deficiency reduced the levels of Th17 cells and CD103⁺ DCs, which are implicated in IgA regulation. PARP14 enhanced the expression of RORα, Runx1, and Smad3 after T cell activation, and, importantly, its catalytic activity of PARP14 promoted Th17 differentiation. Collectively, the findings show that PARP14 influences the class distribution, affinity repertoire, and recall capacity of Ab responses in mice, as well as provide direct evidence of the requirement for protein mono-ADP-ribosylation in Th cell differentiation.
Files in This Item:
T201400201.pdf Download
DOI
10.4049/jimmunol.1301106
Appears in Collections:
1. College of Medicine (의과대학) > BioMedical Science Institute (의생명과학부) > 1. Journal Papers
Yonsei Authors
Nam, Ki Taek(남기택)
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/98036
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