AAV-mediated BMP7 gene therapy counteracts insulin resistance and obesity
Type 2 diabetes, insulin resistance, and obesity are strongly associated and are a major health problem worldwide. Obesity largely results from a sustained imbalance between energy intake and expenditure. Therapeutic approaches targeting metabolic rate may counteract body weight gain and insulin res...
| Autores: | , , , , , , , , , , , , , , , |
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| Tipo de recurso: | artículo |
| Fecha de publicación: | 2022 |
| País: | España |
| Institución: | Universitat Autònoma de Barcelona |
| Repositorio: | Dipòsit Digital de Documents de la UAB |
| Idioma: | inglés |
| OAI Identifier: | oai:ddd.uab.cat:258120 |
| Acceso en línea: | https://ddd.uab.cat/record/258120 https://dx.doi.org/urn:doi:10.1016/j.omtm.2022.03.007 |
| Access Level: | acceso abierto |
| Palabra clave: | AAV Gene therapy Obesity Type 2 diabetes BMP7 Insulin resistance |
| Sumario: | Type 2 diabetes, insulin resistance, and obesity are strongly associated and are a major health problem worldwide. Obesity largely results from a sustained imbalance between energy intake and expenditure. Therapeutic approaches targeting metabolic rate may counteract body weight gain and insulin resistance. Bone morphogenic protein 7 (BMP7) has proven to enhance energy expenditure by inducing non-shivering thermogenesis in short-term studies in mice treated with the recombinant protein or adenoviral vectors encoding BMP7. To achieve long-term BMP7 effects, the use of adeno-associated viral (AAV) vectors would provide sustained production of the protein after a single administration. Here, we demonstrated that treatment of high-fat-diet-fed mice and ob/ob mice with liver-directed AAV-BMP7 vectors enabled a long-lasting increase in circulating levels of this factor. This rise in BMP7 concentration induced browning of white adipose tissue (WAT) and activation of brown adipose tissue, which enhanced energy expenditure, and reversed WAT hypertrophy, hepatic steatosis, and WAT and liver inflammation, ultimately resulting in normalization of body weight and insulin resistance. This study highlights the potential of AAV-BMP7-mediated gene therapy for the treatment of insulin resistance, type 2 diabetes, and obesity. HFD-fed and ob/ob mice treated with liver-directed AAV-BMP7 vectors showed increased serum BMP7, which induced energy expenditure and reversed WAT hypertrophy, hepatic steatosis, and WAT and liver inflammation, resulting in body weight normalization and insulin sensitivity. This study highlights the potential of AAV-BMP7-mediated gene therapy to treat insulin resistance and obesity. |
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