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CRISPR/Cas9 editing in conditionally immortalized HoxB8 cells for studying gene regulation in mouse dendritic cells.
Xu, Huaming; Look, Thomas; Prithiviraj, Sujeethkumar; Lennartz, Daniel; Cáceres, Manuel Delgado; Götz, Katrin; Wanek, Paul; Häcker, Hans; Kramann, Rafael; Seré, Kristin; Zenke, Martin.
Afiliação
  • Xu H; Department of Cell Biology, Institute of Biomedical Engineering, RWTH Aachen University Medical School, Aachen, Germany.
  • Look T; Helmholtz Institute for Biomedical Engineering, RWTH Aachen University, Aachen, Germany.
  • Prithiviraj S; Department of Cell Biology, Institute of Biomedical Engineering, RWTH Aachen University Medical School, Aachen, Germany.
  • Lennartz D; Helmholtz Institute for Biomedical Engineering, RWTH Aachen University, Aachen, Germany.
  • Cáceres MD; Department of Cell Biology, Institute of Biomedical Engineering, RWTH Aachen University Medical School, Aachen, Germany.
  • Götz K; Helmholtz Institute for Biomedical Engineering, RWTH Aachen University, Aachen, Germany.
  • Wanek P; Department of Cell Biology, Institute of Biomedical Engineering, RWTH Aachen University Medical School, Aachen, Germany.
  • Häcker H; Helmholtz Institute for Biomedical Engineering, RWTH Aachen University, Aachen, Germany.
  • Kramann R; Department of Cell Biology, Institute of Biomedical Engineering, RWTH Aachen University Medical School, Aachen, Germany.
  • Seré K; Helmholtz Institute for Biomedical Engineering, RWTH Aachen University, Aachen, Germany.
  • Zenke M; Department of Cell Biology, Institute of Biomedical Engineering, RWTH Aachen University Medical School, Aachen, Germany.
Eur J Immunol ; 52(11): 1859-1862, 2022 11.
Article em En | MEDLINE | ID: mdl-34826338
ABSTRACT
HoxB8 multipotent progenitors (MPP) are obtained by expression of the estrogen receptor hormone binding domain (ERHBD) HoxB8 fusion gene in mouse BM cells. HoxB8 MPP generate (i) the full complement of DC subsets (cDC1, cDC2, and pDC) in vitro and in vivo and (ii) allow CRISPR/Cas9-mediated gene editing, for example, generating homozygous deletions in cis-acting DNA elements at high precision, and (iii) efficient gene repression by dCas9-KRAB for studying gene regulation in DC differentiation.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sistemas CRISPR-Cas / Edição de Genes Limite: Animals Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sistemas CRISPR-Cas / Edição de Genes Limite: Animals Idioma: En Ano de publicação: 2022 Tipo de documento: Article