Normoglycemia partially recovers the disrupted osteoblast differentiation of mesenchymal stem cells induced by type 1 but not type 2 diabetes mellitus.
Denise WeffortLeticia F AdolphoAlann T P SouzaGileade P FreitasHelena B LopesFabiola S OliveiraRayana L Bighetti-TrevisanLeticia Pitol-PalinDoris H MatsushitaRoberta OkamotoAdalberto Luiz RosaAdalberto Luiz RosaPublished in: Journal of cellular biochemistry (2023)
Type 1 (T1DM) and type 2 (T2DM) diabetes mellitus are characterized by changes in glucose metabolism and cause bone damage via a variety of mechanisms, including effects on osteoblasts. We aimed to evaluate the osteoblast differentiation of mesenchymal stem cells (MSCs) from rats with T1DM or T2DM and the effects of removing the hyperglycemic stimulus on the osteogenic potential of these cells. MSCs from healthy rats were cultured in normoglycemic medium, whereas MSCs from rats with T1DM or T2DM were cultured in hyperglycemic or normoglycemic medium. T1DM and T2DM reduced osteoblast differentiation of MSCs grown in hyperglycemic media, with T1DM having a more pronounced effect, as evidenced by alkaline phosphatase activity, RUNX2 protein expression, and extracellular matrix mineralization, and modulated the gene expression of several components of the bone morphogenetic protein signaling pathway. The restoration of the normoglycemic environment partially recovers the osteogenic potential of MSCs from rats with T1DM but not with T2DM. Our findings highlight the need for specific therapies to treat T1DM- or T2DM-induced bone loss, as both disrupt osteoblast differentiation at distinct levels and likely through different mechanisms.
Keyphrases
- mesenchymal stem cells
- glycemic control
- umbilical cord
- gene expression
- signaling pathway
- extracellular matrix
- bone marrow
- type diabetes
- bone loss
- cardiovascular disease
- cell therapy
- oxidative stress
- bone regeneration
- endothelial cells
- induced apoptosis
- cell proliferation
- pi k akt
- epithelial mesenchymal transition
- risk assessment
- cardiovascular risk factors
- endoplasmic reticulum stress
- drug induced
- transcription factor