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CD47 and thrombospondin-1 regulation of mitochondria, metabolism, and diabetes.
Roberts, David D; Isenberg, Jeffrey S.
Affiliation
  • Roberts DD; Laboratory of Pathology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.
  • Isenberg JS; Radiation Control Technologies, Inc., Loudonville, New York.
Am J Physiol Cell Physiol ; 321(2): C201-C213, 2021 08 01.
Article in En | MEDLINE | ID: mdl-34106789
ABSTRACT
Thrombospondin-1 (TSP1) is the prototypical member of a family of secreted proteins that modulate cell behavior by engaging with molecules in the extracellular matrix and with receptors on the cell surface. CD47 is widely displayed on many, if not all, cell types and is a high-affinity TSP1 receptor. CD47 is a marker of self that limits innate immune cell activities, a feature recently exploited to enhance cancer immunotherapy. Another major role for CD47 in health and disease is to mediate TSP1 signaling. TSP1 acting through CD47 contributes to mitochondrial, metabolic, and endocrine dysfunction. Studies in animal models found that elevated TSP1 expression, acting in part through CD47, causes mitochondrial and metabolic dysfunction. Clinical studies established that abnormal TSP1 expression positively correlates with obesity, fatty liver disease, and diabetes. The unabated increase in these conditions worldwide and the availability of CD47 targeting drugs justify a closer look into how TSP1 and CD47 disrupt metabolic balance and the potential for therapeutic intervention.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Thrombospondin 1 / Endothelial Cells / Diabetes Mellitus / CD47 Antigen / Mitochondria Limits: Animals / Humans Language: En Journal: Am J Physiol Cell Physiol Journal subject: FISIOLOGIA Year: 2021 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Thrombospondin 1 / Endothelial Cells / Diabetes Mellitus / CD47 Antigen / Mitochondria Limits: Animals / Humans Language: En Journal: Am J Physiol Cell Physiol Journal subject: FISIOLOGIA Year: 2021 Document type: Article