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Expression of the Discoidin Domain Receptor Family Depended on Glucose and Their High Expression in Arterial Tissues in the Rat Model of Type 2 Diabetes.
- Source :
-
Biological & pharmaceutical bulletin [Biol Pharm Bull] 2024; Vol. 47 (7), pp. 1288-1295. - Publication Year :
- 2024
-
Abstract
- The active form of discoidin domain receptors (DDRs) is expressed in cell surface and regulated post-translationally by glucose. The DDR2 and DDR1 transfected in HEK293 cells were expressed mainly in their active forms with sizes of 130 and 120 kDa, respectively. DDRs were observed predominantly as 100 kDa proteins in glucose-depleted culture conditions. However, transfection of endothelial growth factor receptor (EGFR) in HEK293 cells resulted in the expression of only one form regardless of glucose concentration. Vascular smooth muscle cells, HT1080s, and MDA-MB-231 cancer cells expressed DDRs in their active forms in high glucose concentrations, which did not occur with EGFR. In diabetic rats, DDRs were expressed at high levels in arterial tissue but EGFR was not highly expressed. Taken together, these results suggest that DDRs expression depends on glucose concentration it may cooperate in the development of atherosclerosis and kidney fibroblasts, promoting nephropathy in diabetic rats.
- Subjects :
- Animals
Humans
Male
HEK293 Cells
Rats
Arteries metabolism
Arteries pathology
ErbB Receptors metabolism
ErbB Receptors genetics
Cell Line, Tumor
Discoidin Domain Receptor 2 metabolism
Discoidin Domain Receptor 2 genetics
Muscle, Smooth, Vascular metabolism
Receptor Protein-Tyrosine Kinases metabolism
Receptor Protein-Tyrosine Kinases genetics
Rats, Wistar
Glucose metabolism
Diabetes Mellitus, Type 2 metabolism
Diabetes Mellitus, Type 2 genetics
Diabetes Mellitus, Experimental metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1347-5215
- Volume :
- 47
- Issue :
- 7
- Database :
- MEDLINE
- Journal :
- Biological & pharmaceutical bulletin
- Publication Type :
- Academic Journal
- Accession number :
- 39010214
- Full Text :
- https://doi.org/10.1248/bpb.b24-00245