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CD36 Signal Transduction in Metabolic Diseases: Novel Insights and Therapeutic Targeting.
- Source :
-
Cells [Cells] 2021 Jul 20; Vol. 10 (7). Date of Electronic Publication: 2021 Jul 20. - Publication Year :
- 2021
-
Abstract
- The cluster of differentiation 36 (CD36) is a scavenger receptor present on various types of cells and has multiple biological functions that may be important in inflammation and in the pathogenesis of metabolic diseases, including diabetes. Here, we consider recent insights into how the CD36 response becomes deregulated under metabolic conditions, as well as the therapeutic benefits of CD36 inhibition, which may provide clues for developing strategies aimed at the treatment or prevention of diabetes associated with metabolic diseases. To facilitate this process further, it is important to pinpoint regulatory mechanisms that are relevant under physiological and pathological conditions. In particular, understanding the mechanisms involved in dictating specific CD36 downstream cellular outcomes will aid in the discovery of potent compounds that target specific CD36 downstream signaling cascades.
- Subjects :
- Amyloid metabolism
Anti-Inflammatory Agents therapeutic use
CD36 Antigens antagonists & inhibitors
CD36 Antigens genetics
Diabetes Mellitus drug therapy
Diabetes Mellitus genetics
Diabetes Mellitus pathology
Fatty Acids metabolism
Gene Expression Regulation
Humans
Hyperglycemia drug therapy
Hyperglycemia genetics
Hyperglycemia pathology
Inflammation
Insulin metabolism
Insulin Receptor Substrate Proteins genetics
Insulin Receptor Substrate Proteins metabolism
Insulin Resistance
Insulin-Secreting Cells drug effects
Insulin-Secreting Cells pathology
Lipoproteins, LDL metabolism
Molecular Targeted Therapy
NF-kappa B genetics
NF-kappa B metabolism
Reactive Oxygen Species antagonists & inhibitors
CD36 Antigens metabolism
Diabetes Mellitus metabolism
Hyperglycemia metabolism
Insulin-Secreting Cells metabolism
Reactive Oxygen Species metabolism
Signal Transduction genetics
Subjects
Details
- Language :
- English
- ISSN :
- 2073-4409
- Volume :
- 10
- Issue :
- 7
- Database :
- MEDLINE
- Journal :
- Cells
- Publication Type :
- Academic Journal
- Accession number :
- 34360006
- Full Text :
- https://doi.org/10.3390/cells10071833