| First Author | Kim SN | Year | 2017 |
| Journal | Sci Rep | Volume | 7 |
| Issue | 1 | Pages | 7159 |
| PubMed ID | 28769076 | Mgi Jnum | J:267117 |
| Mgi Id | MGI:6258967 | Doi | 10.1038/s41598-017-07658-y |
| Citation | Kim SN, et al. (2017) Connexin 43 is required for the maintenance of mitochondrial integrity in brown adipose tissue. Sci Rep 7(1):7159 |
| abstractText | We investigated the role of connexin 43 (Cx43) in maintaining the integrity of mitochondria in brown adipose tissue (BAT). The functional effects of Cx43 were evaluated using inducible, adipocyte-specific Cx43 knockout in mice (Gja1 (adipoq) KO) and by overexpression and knockdown of Cx43 in cultured adipocytes. Mitochondrial morphology was evaluated by electron microscopy and mitochondrial function and autophagy were assessed by immunoblotting, immunohistochemistry, and qPCR. The metabolic effects of adipocyte-specific knockout of Cx43 were assessed during cold stress and following high fat diet feeding. Cx43 expression was higher in BAT compared to white adipose tissue. Treatment with the beta3-adrenergic receptor agonist CL316,243 increased Cx43 expression and mitochondrial localization. Gja1 (adipoq) KO mice reduced mitochondrial density and increased the presence of damaged mitochondria in BAT. Moreover, metabolic activation with CL316,243 further reduced mitochondrial integrity and upregulated autophagy in the BAT of Gja1 (adipoq) KO mice. Inhibition of Cx43 in cultured adipocytes increased the generation of reactive oxygen species and induction of autophagy during beta-adrenergic stimulation. Gja1 (adipoq) KO mice were cold intolerant, expended less energy in response to beta3-adrenergic receptor activation, and were more insulin resistant after a high-fat diet challenge. Collectively, our data demonstrate that Cx43 is required for maintaining the mitochondrial integrity and metabolic activity of BAT. |
