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Context-Dependent Development of Lymphoid Stroma from Adult CD34(+) Adventitial Progenitors.
Sitnik, Katarzyna M; Wendland, Kerstin; Weishaupt, Holger; Uronen-Hansson, Heli; White, Andrea J; Anderson, Graham; Kotarsky, Knut; Agace, William W.
Afiliação
  • Sitnik KM; Section for Immunology and Vaccinology, National Veterinary Institute, Technical University of Denmark, Bülowsvej 27, 1870 Frederiksberg C, Denmark. Electronic address: kasit@vet.dtu.dk.
  • Wendland K; Immunology Section, Lund University, BMC D14, 221-84 Lund, Sweden.
  • Weishaupt H; Department of Immunology, Genetics, and Pathology, Rudbecklaboratoriet, Uppsala University, 751-85 Uppsala, Sweden.
  • Uronen-Hansson H; Immunology Section, Lund University, BMC D14, 221-84 Lund, Sweden.
  • White AJ; Medical Research Council Centre for Immune Regulation, Institute for Biomedical Research, University of Birmingham, Birmingham B15 2TT, UK.
  • Anderson G; Medical Research Council Centre for Immune Regulation, Institute for Biomedical Research, University of Birmingham, Birmingham B15 2TT, UK.
  • Kotarsky K; Immunology Section, Lund University, BMC D14, 221-84 Lund, Sweden.
  • Agace WW; Section for Immunology and Vaccinology, National Veterinary Institute, Technical University of Denmark, Bülowsvej 27, 1870 Frederiksberg C, Denmark; Immunology Section, Lund University, BMC D14, 221-84 Lund, Sweden. Electronic address: william.agace@med.lu.se.
Cell Rep ; 14(10): 2375-88, 2016 Mar 15.
Article em En | MEDLINE | ID: mdl-26947077
ABSTRACT
Despite the key role of primary and secondary lymphoid organ stroma in immunity, our understanding of the heterogeneity and ontogeny of these cells remains limited. Here, we identify a functionally distinct subset of BP3(-)PDPN(+)PDGFRß(+)/α(+)CD34(+) stromal adventitial cells in both lymph nodes (LNs) and thymus that is located within the vascular niche surrounding PDPN(-)PDGFRß(+)/α(-)Esam-1(+)ITGA7(+) pericytes. CD34(+) adventitial cells developed in late embryonic thymus and in postnatal LNs and in the thymus originated, along with pericytes, from a common anlage-seeding progenitor population. Using lymphoid organ re-aggregate grafts, we demonstrate that adult CD34(+) adventitial cells are capable of differentiating into multiple lymphoid stroma-like subsets including pericyte-, FRC-, MRC-, and FDC-like cells, the development of which was lymphoid environment-dependent. These findings extend the current understanding of lymphoid mesenchymal cell heterogeneity and highlight a role of the CD34(+) adventitia as a potential ubiquitous source of lymphoid stromal precursors in postnatal tissues.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Células Estromais / Antígenos CD34 Tipo de estudo: Prognostic_studies Idioma: En Revista: Cell Rep Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Células Estromais / Antígenos CD34 Tipo de estudo: Prognostic_studies Idioma: En Revista: Cell Rep Ano de publicação: 2016 Tipo de documento: Article