| First Author | Wang F | Year | 2017 |
| Journal | Nat Commun | Volume | 8 |
| Pages | 15182 | PubMed ID | 28474670 |
| Mgi Jnum | J:250342 | Mgi Id | MGI:5920600 |
| Doi | 10.1038/ncomms15182 | Citation | Wang F, et al. (2017) Protein kinase C-alpha suppresses autophagy and induces neural tube defects via miR-129-2 in diabetic pregnancy. Nat Commun 8:15182 |
| abstractText | Gene deletion-induced autophagy deficiency leads to neural tube defects (NTDs), similar to those in diabetic pregnancy. Here we report the key autophagy regulators modulated by diabetes in the murine developing neuroepithelium. Diabetes predominantly leads to exencephaly, induces neuroepithelial cell apoptosis and suppresses autophagy in the forebrain and midbrain of NTD embryos. Deleting the Prkca gene, which encodes PKCalpha, reverses diabetes-induced autophagy impairment, cellular organelle stress and apoptosis, leading to an NTD reduction. PKCalpha increases the expression of miR-129-2, which is a negative regulator of autophagy. miR-129-2 represses autophagy by directly targeting PGC-1alpha, a positive regulator for mitochondrial function, which is disturbed by maternal diabetes. PGC-1alpha supports neurulation by stimulating autophagy in neuroepithelial cells. These findings identify two negative autophagy regulators, PKCalpha and miR-129-2, which mediate the teratogenicity of hyperglycaemia leading to NTDs. We also reveal a function for PGC-1alpha in embryonic development through promoting autophagy and ameliorating hyperglycaemia-induced NTDs. |
