Deficiency of the oxidative damage-specific DNA glycosylase NEIL1 leads to reduced germinal center B cell expansion

Hiromi Mori, Rika Ouchida, Atsushi Hijikata, Hiroshi Kitamura, Osamu Ohara, Yingqian Li, Xiang Gao, Akira Yasui, Robert (Stephen) Lloyd, Ji Yang Wang

Research output: Contribution to journalArticle

17 Citations (Scopus)

Abstract

Mammalian cells possess multiple DNA glycosylases, including OGG1, NTH1, NEIL1, NEIL2 and NEIL3, for the repair of oxidative DNA damage. Among these, NEIL1 and NEIL2 are able to excise oxidized bases on single stranded or bubble-structured DNA and has been implicated in repair of oxidative damage associated with DNA replication or transcription. We found that Neil1 was highly constitutively expressed in the germinal center (GC) B cells, a rapidly dividing cell population that is undergoing immunoglobulin (Ig) gene hypermutation and isotype switching. While Neil1-/- mice exhibited normal B and T cell development and maturation, these mice contained a significantly lower frequency of GC B cells than did WT mice after immunization with a T-dependent antigen. Consistent with the reduced expansion of GC B cells, Neil1-/- mice had a decreased frequency of Ig gene hypermutation and produced less antibody against a T-dependent antigen during both primary and secondary immune responses. These results suggest that repair of endogenous oxidative DNA damage by NEIL1 is important for the rapid expansion of GC B cells and efficient induction of humoral immune responses.

Original languageEnglish (US)
Pages (from-to)1328-1332
Number of pages5
JournalDNA Repair
Volume8
Issue number11
DOIs
StatePublished - Nov 2 2009

Fingerprint

DNA Glycosylases
Germinal Center
B-Lymphocytes
Cells
Immunoglobulin Genes
Viral Tumor Antigens
Repair
DNA
DNA Damage
Immunoglobulins
Immunoglobulin Class Switching
Genes
Immunoglobulin Isotypes
Immunization
Antigens
Humoral Immunity
DNA Replication
T-cells
Transcription
T-Lymphocytes

Keywords

  • DNA glycosylase
  • Germinal center B cells
  • Immune response
  • Oxidative damage
  • Somatic hypermutation

ASJC Scopus subject areas

  • Biochemistry
  • Molecular Biology
  • Cell Biology

Cite this

Mori, H., Ouchida, R., Hijikata, A., Kitamura, H., Ohara, O., Li, Y., ... Wang, J. Y. (2009). Deficiency of the oxidative damage-specific DNA glycosylase NEIL1 leads to reduced germinal center B cell expansion. DNA Repair, 8(11), 1328-1332. https://doi.org/10.1016/j.dnarep.2009.08.007

Deficiency of the oxidative damage-specific DNA glycosylase NEIL1 leads to reduced germinal center B cell expansion. / Mori, Hiromi; Ouchida, Rika; Hijikata, Atsushi; Kitamura, Hiroshi; Ohara, Osamu; Li, Yingqian; Gao, Xiang; Yasui, Akira; Lloyd, Robert (Stephen); Wang, Ji Yang.

In: DNA Repair, Vol. 8, No. 11, 02.11.2009, p. 1328-1332.

Research output: Contribution to journalArticle

Mori, H, Ouchida, R, Hijikata, A, Kitamura, H, Ohara, O, Li, Y, Gao, X, Yasui, A, Lloyd, RS & Wang, JY 2009, 'Deficiency of the oxidative damage-specific DNA glycosylase NEIL1 leads to reduced germinal center B cell expansion', DNA Repair, vol. 8, no. 11, pp. 1328-1332. https://doi.org/10.1016/j.dnarep.2009.08.007
Mori, Hiromi ; Ouchida, Rika ; Hijikata, Atsushi ; Kitamura, Hiroshi ; Ohara, Osamu ; Li, Yingqian ; Gao, Xiang ; Yasui, Akira ; Lloyd, Robert (Stephen) ; Wang, Ji Yang. / Deficiency of the oxidative damage-specific DNA glycosylase NEIL1 leads to reduced germinal center B cell expansion. In: DNA Repair. 2009 ; Vol. 8, No. 11. pp. 1328-1332.
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