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Regulation of the T Cell Response by CD39.
Takenaka, Maisa C; Robson, Simon; Quintana, Francisco J.
Afiliação
  • Takenaka MC; Ann Romney Center for Neurologic Diseases, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
  • Robson S; Divisions of Gastroenterology, Hepatology, and Transplantation, Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA. Electronic address: srobson@bidmc.harvard.edu.
  • Quintana FJ; Ann Romney Center for Neurologic Diseases, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA; Broad Institute of Massachusetts Institute of Technology (MIT) and Harvard, Cambridge, MA, USA. Electronic address: fquintana@rics.bwh.harvard.edu.
Trends Immunol ; 37(7): 427-439, 2016 07.
Article em En | MEDLINE | ID: mdl-27236363
ABSTRACT
The ectonucleoside triphosphate diphosphohydrolase 1 (ENTPD1, or CD39) catalyzes the phosphohydrolysis of extracellular ATP (eATP) and ADP (eADP) released under conditions of inflammatory stress and cell injury. CD39 generates AMP, which is in turn used by the ecto-5'-nucleotidase CD73 to synthesize adenosine. These ectonucleotidases have a major impact on the dynamic equilibrium of proinflammatory eATP and ADP nucleotides versus immunosuppressive adenosine nucleosides. Indeed, CD39 plays a dominant role in the purinergic regulation of inflammation and the immune response because its expression is influenced by genetic and environmental factors. We review the specific role of CD39 in the kinetic regulation of cellular immune responses in the evolution of disease. We focus on the effects of CD39 on T cells and explore potential clinical applications in autoimmunity, chronic infections, and cancer.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Apirase / Doenças Autoimunes / Linfócitos T / Antígenos CD / Tolerância Imunológica / Infecções / Inflamação / Neoplasias Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Apirase / Doenças Autoimunes / Linfócitos T / Antígenos CD / Tolerância Imunológica / Infecções / Inflamação / Neoplasias Idioma: En Ano de publicação: 2016 Tipo de documento: Article