Gβγ-SNAP25 exocytotic brake removal enhances insulin action, promotes adipocyte browning, and protects against diet-induced obesity
Negative regulation of exocytosis from secretory cells is accomplished through inhibitory signals from Gi/o GPCRs by Gβγ subunit inhibition of 2 mechanisms: decreased calcium entry and direct interaction of Gβγ with soluble N-ethylmaleimide–sensitive factor attachment protein (SNAP) receptor (SNARE)...
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Format: | Article |
Language: | English |
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American Society for Clinical Investigation
2023-10-01
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Series: | The Journal of Clinical Investigation |
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Online Access: | https://doi.org/10.1172/JCI160617 |
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author | Ryan P. Ceddia Zack Zurawski Analisa Thompson Gray Feyisayo Adegboye Ainsley McDonald-Boyer Fubiao Shi Dianxin Liu Jose Maldonado Jiesi Feng Yulong Li Simon Alford Julio E. Ayala Owen P. McGuinness Sheila Collins Heidi E. Hamm |
author_facet | Ryan P. Ceddia Zack Zurawski Analisa Thompson Gray Feyisayo Adegboye Ainsley McDonald-Boyer Fubiao Shi Dianxin Liu Jose Maldonado Jiesi Feng Yulong Li Simon Alford Julio E. Ayala Owen P. McGuinness Sheila Collins Heidi E. Hamm |
author_sort | Ryan P. Ceddia |
collection | DOAJ |
description | Negative regulation of exocytosis from secretory cells is accomplished through inhibitory signals from Gi/o GPCRs by Gβγ subunit inhibition of 2 mechanisms: decreased calcium entry and direct interaction of Gβγ with soluble N-ethylmaleimide–sensitive factor attachment protein (SNAP) receptor (SNARE) plasma membrane fusion machinery. Previously, we disabled the second mechanism with a SNAP25 truncation (SNAP25Δ3) that decreased Gβγ affinity for the SNARE complex, leaving exocytotic fusion and modulation of calcium entry intact and removing GPCR-Gβγ inhibition of SNARE-mediated exocytosis. Here, we report substantial metabolic benefit in mice carrying this mutation. Snap25Δ3/Δ3 mice exhibited enhanced insulin sensitivity and beiging of white fat. Metabolic protection was amplified in Snap25Δ3/Δ3 mice challenged with a high-fat diet. Glucose homeostasis, whole-body insulin action, and insulin-mediated glucose uptake into white adipose tissue were improved along with resistance to diet-induced obesity. Metabolic protection in Snap25Δ3/Δ3 mice occurred without compromising the physiological response to fasting or cold. All metabolic phenotypes were reversed at thermoneutrality, suggesting that basal autonomic activity was required. Direct electrode stimulation of sympathetic neuron exocytosis from Snap25Δ3/Δ3 inguinal adipose depots resulted in enhanced and prolonged norepinephrine release. Thus, the Gβγ-SNARE interaction represents a cellular mechanism that deserves further exploration as an additional avenue for combating metabolic disease. |
first_indexed | 2024-03-11T12:08:02Z |
format | Article |
id | doaj.art-a5ee21a0d0b84d4e9b842e9bacb8ba19 |
institution | Directory Open Access Journal |
issn | 1558-8238 |
language | English |
last_indexed | 2024-03-11T12:08:02Z |
publishDate | 2023-10-01 |
publisher | American Society for Clinical Investigation |
record_format | Article |
series | The Journal of Clinical Investigation |
spelling | doaj.art-a5ee21a0d0b84d4e9b842e9bacb8ba192023-11-07T16:20:55ZengAmerican Society for Clinical InvestigationThe Journal of Clinical Investigation1558-82382023-10-0113319Gβγ-SNAP25 exocytotic brake removal enhances insulin action, promotes adipocyte browning, and protects against diet-induced obesityRyan P. CeddiaZack ZurawskiAnalisa Thompson GrayFeyisayo AdegboyeAinsley McDonald-BoyerFubiao ShiDianxin LiuJose MaldonadoJiesi FengYulong LiSimon AlfordJulio E. AyalaOwen P. McGuinnessSheila CollinsHeidi E. HammNegative regulation of exocytosis from secretory cells is accomplished through inhibitory signals from Gi/o GPCRs by Gβγ subunit inhibition of 2 mechanisms: decreased calcium entry and direct interaction of Gβγ with soluble N-ethylmaleimide–sensitive factor attachment protein (SNAP) receptor (SNARE) plasma membrane fusion machinery. Previously, we disabled the second mechanism with a SNAP25 truncation (SNAP25Δ3) that decreased Gβγ affinity for the SNARE complex, leaving exocytotic fusion and modulation of calcium entry intact and removing GPCR-Gβγ inhibition of SNARE-mediated exocytosis. Here, we report substantial metabolic benefit in mice carrying this mutation. Snap25Δ3/Δ3 mice exhibited enhanced insulin sensitivity and beiging of white fat. Metabolic protection was amplified in Snap25Δ3/Δ3 mice challenged with a high-fat diet. Glucose homeostasis, whole-body insulin action, and insulin-mediated glucose uptake into white adipose tissue were improved along with resistance to diet-induced obesity. Metabolic protection in Snap25Δ3/Δ3 mice occurred without compromising the physiological response to fasting or cold. All metabolic phenotypes were reversed at thermoneutrality, suggesting that basal autonomic activity was required. Direct electrode stimulation of sympathetic neuron exocytosis from Snap25Δ3/Δ3 inguinal adipose depots resulted in enhanced and prolonged norepinephrine release. Thus, the Gβγ-SNARE interaction represents a cellular mechanism that deserves further exploration as an additional avenue for combating metabolic disease.https://doi.org/10.1172/JCI160617EndocrinologyMetabolism |
spellingShingle | Ryan P. Ceddia Zack Zurawski Analisa Thompson Gray Feyisayo Adegboye Ainsley McDonald-Boyer Fubiao Shi Dianxin Liu Jose Maldonado Jiesi Feng Yulong Li Simon Alford Julio E. Ayala Owen P. McGuinness Sheila Collins Heidi E. Hamm Gβγ-SNAP25 exocytotic brake removal enhances insulin action, promotes adipocyte browning, and protects against diet-induced obesity The Journal of Clinical Investigation Endocrinology Metabolism |
title | Gβγ-SNAP25 exocytotic brake removal enhances insulin action, promotes adipocyte browning, and protects against diet-induced obesity |
title_full | Gβγ-SNAP25 exocytotic brake removal enhances insulin action, promotes adipocyte browning, and protects against diet-induced obesity |
title_fullStr | Gβγ-SNAP25 exocytotic brake removal enhances insulin action, promotes adipocyte browning, and protects against diet-induced obesity |
title_full_unstemmed | Gβγ-SNAP25 exocytotic brake removal enhances insulin action, promotes adipocyte browning, and protects against diet-induced obesity |
title_short | Gβγ-SNAP25 exocytotic brake removal enhances insulin action, promotes adipocyte browning, and protects against diet-induced obesity |
title_sort | gβγ snap25 exocytotic brake removal enhances insulin action promotes adipocyte browning and protects against diet induced obesity |
topic | Endocrinology Metabolism |
url | https://doi.org/10.1172/JCI160617 |
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