Your browser doesn't support javascript.
loading
Quantitative trait loci mapping provides insights into the genetic regulation of dendritic cell numbers in mouse tissues.
Oliveira, Thiago Y; Merkenschlager, Julia; Eisenreich, Thomas; Bortolatto, Juliana; Yao, Kai-Hui; Gatti, Daniel M; Churchill, Gary A; Nussenzweig, Michel C; Breton, Gaëlle.
Affiliation
  • Oliveira TY; Laboratory of Molecular Immunology, The Rockefeller University, New York, NY 10065, USA.
  • Merkenschlager J; Laboratory of Molecular Immunology, The Rockefeller University, New York, NY 10065, USA.
  • Eisenreich T; Laboratory of Molecular Immunology, The Rockefeller University, New York, NY 10065, USA.
  • Bortolatto J; Laboratory of Lymphocyte Dynamics, The Rockefeller University, New York, NY 10065, USA.
  • Yao KH; Laboratory of Molecular Immunology, The Rockefeller University, New York, NY 10065, USA.
  • Gatti DM; The Jackson Laboratory, Bar Harbor, ME 04609, USA.
  • Churchill GA; The Jackson Laboratory, Bar Harbor, ME 04609, USA.
  • Nussenzweig MC; Laboratory of Molecular Immunology, The Rockefeller University, New York, NY 10065, USA; Howard Hughes Medical Institute (HHMI), The Rockefeller University, New York, NY 10065, USA. Electronic address: nussen@rockefeller.edu.
  • Breton G; Laboratory of Molecular Immunology, The Rockefeller University, New York, NY 10065, USA. Electronic address: gbreton@rockefeller.edu.
Cell Rep ; 43(6): 114296, 2024 Jun 25.
Article in En | MEDLINE | ID: mdl-38823019
ABSTRACT
To explore the influence of genetics on homeostatic regulation of dendritic cell (DC) numbers, we present a screen of DCs and their progenitors in lymphoid and non-lymphoid tissues in Collaborative Cross (CC) and Diversity Outbred (DO) mice. We report 30 and 71 loci with logarithm of the odds (LOD) scores >8.18 and ranging from 6.67 to 8.19, respectively. The analysis reveals the highly polygenic and pleiotropic architecture of this complex trait, including many of the previously identified genetic regulators of DC development and maturation. Two SNPs in genes potentially underlying variation in DC homeostasis, a splice variant in Gramd4 (rs235532740) and a missense variant in Orai3 (rs216659754), are confirmed by gene editing using CRISPR-Cas9. Gramd4 is a central regulator of DC homeostasis that impacts the entire DC lineage, and Orai3 regulates cDC2 numbers in tissues. Overall, the data reveal a large number of candidate genes regulating DC homeostasis in vivo.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Dendritic Cells / Quantitative Trait Loci Limits: Animals Language: En Journal: Cell Rep Year: 2024 Document type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Dendritic Cells / Quantitative Trait Loci Limits: Animals Language: En Journal: Cell Rep Year: 2024 Document type: Article Affiliation country: United States