Y chromosome-linked B and NK cell deficiency in mice

Shu Lan Sun, Satoshi Horino, Ari Itoh-Nakadai, Takeshi Kawabe, Atsuko Asao, Takeshi Takahashi, Takanori So, Ryo Funayama, Motonari Kondo, Hirotomo Saitsu, Naomichi Matsumoto, Keiko Nakayama, Naoto Ishii

Research output: Contribution to journalArticlepeer-review

11 Citations (Scopus)

Abstract

There are no primary immunodeficiency diseases linked to the Y chromosome, because the Y chromosome does not contain any vital genes. We have established a novel mouse strain inwhich all males lack B and NK cells and have Peyer's patch defects. By 10 wk of age, 100% of the males had evident immunodeficiencies. Mating these immunodeficient males with wild-type females on two different genetic backgrounds for several generations demonstrated that the immunodeficiency is linked to the Y chromosome and is inherited in a Mendelian fashion. Although multicolor fluorescence in situ hybridization analysis showed that the Y chromosome in the mutant male mice was one third shorter than that in wild-type males, exome sequencing did not identify any significant gene mutations. The precise molecular mechanisms are still unknown. Bone marrow chimeric analyses demonstrated that an intrinsic abnormality in bone marrow hematopoietic cells causes the B and NK cell defects. Interestingly, fetal liver cells transplanted from the mutant male mice reconstituted B and NK cells in lymphocyte-deficient Il2rg-/- recipient mice, whereas adult bone marrow transplants did not. Transducing the EBF gene, a master transcription factor for B cell development, into mutant hematopoietic progenitor cells rescued B cell but not NK cell development both in vitro and in vivo. These Y chromosome-linked immunodeficient mice, which have preferential B and NK cell defects, may be a useful model of lymphocyte development.

Original languageEnglish
Pages (from-to)6209-6220
Number of pages12
JournalJournal of Immunology
Volume190
Issue number12
DOIs
Publication statusPublished - 2013 Jun 15

ASJC Scopus subject areas

  • Immunology and Allergy
  • Immunology

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