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Differential effects of angiopoietin-like 4 in brain and muscle on regulation of lipoprotein lipase activity
OBJECTIVE: Lipoprotein lipase (LPL) is a key regulator of circulating triglyceride rich lipoprotein hydrolysis. In brain LPL regulates appetite and energy expenditure. Angiopoietin-like 4 (Angptl4) is a secreted protein that inhibits LPL activity and, thereby, triglyceride metabolism, but the impact...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4314546/ https://www.ncbi.nlm.nih.gov/pubmed/25685701 http://dx.doi.org/10.1016/j.molmet.2014.11.003 |
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author | Vienberg, Sara Gry Kleinridders, André Suzuki, Ryo Kahn, C. Ronald |
author_facet | Vienberg, Sara Gry Kleinridders, André Suzuki, Ryo Kahn, C. Ronald |
author_sort | Vienberg, Sara Gry |
collection | PubMed |
description | OBJECTIVE: Lipoprotein lipase (LPL) is a key regulator of circulating triglyceride rich lipoprotein hydrolysis. In brain LPL regulates appetite and energy expenditure. Angiopoietin-like 4 (Angptl4) is a secreted protein that inhibits LPL activity and, thereby, triglyceride metabolism, but the impact of Angptl4 on central lipid metabolism is unknown. METHODS: We induced type 1 diabetes by streptozotocin (STZ) in whole-body Angptl4 knockout mice (Angptl4(-/-)) and their wildtype littermates to study the role of Angptl4 in central lipid metabolism. RESULTS: In type 1 (streptozotocin, STZ) and type 2 (ob/ob) diabetic mice, there is a ~2-fold increase of Angptl4 in the hypothalamus and skeletal muscle. Intracerebroventricular insulin injection into STZ mice at levels which have no effect on plasma glucose restores Angptl4 expression in hypothalamus. Isolation of cells from the brain reveals that Angptl4 is produced in glia, whereas LPL is present in both glia and neurons. Consistent with the in vivo experiment, in vitro insulin treatment of glial cells causes a 50% reduction of Angptl4 and significantly increases LPL activity with no change in LPL expression. In Angptl4(-/-) mice, LPL activity in skeletal muscle is increased 3-fold, and this is further increased by STZ-induced diabetes. By contrast, Angptl4(-/-) mice show no significant difference in LPL activity in hypothalamus or brain independent of diabetic and nutritional status. CONCLUSION: Thus, Angptl4 in brain is produced in glia and regulated by insulin. However, in contrast to the periphery, central Angptl4 does not regulate LPL activity, but appears to participate in the metabolic crosstalk between glia and neurons. |
format | Online Article Text |
id | pubmed-4314546 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-43145462015-02-14 Differential effects of angiopoietin-like 4 in brain and muscle on regulation of lipoprotein lipase activity Vienberg, Sara Gry Kleinridders, André Suzuki, Ryo Kahn, C. Ronald Mol Metab Brief Communication OBJECTIVE: Lipoprotein lipase (LPL) is a key regulator of circulating triglyceride rich lipoprotein hydrolysis. In brain LPL regulates appetite and energy expenditure. Angiopoietin-like 4 (Angptl4) is a secreted protein that inhibits LPL activity and, thereby, triglyceride metabolism, but the impact of Angptl4 on central lipid metabolism is unknown. METHODS: We induced type 1 diabetes by streptozotocin (STZ) in whole-body Angptl4 knockout mice (Angptl4(-/-)) and their wildtype littermates to study the role of Angptl4 in central lipid metabolism. RESULTS: In type 1 (streptozotocin, STZ) and type 2 (ob/ob) diabetic mice, there is a ~2-fold increase of Angptl4 in the hypothalamus and skeletal muscle. Intracerebroventricular insulin injection into STZ mice at levels which have no effect on plasma glucose restores Angptl4 expression in hypothalamus. Isolation of cells from the brain reveals that Angptl4 is produced in glia, whereas LPL is present in both glia and neurons. Consistent with the in vivo experiment, in vitro insulin treatment of glial cells causes a 50% reduction of Angptl4 and significantly increases LPL activity with no change in LPL expression. In Angptl4(-/-) mice, LPL activity in skeletal muscle is increased 3-fold, and this is further increased by STZ-induced diabetes. By contrast, Angptl4(-/-) mice show no significant difference in LPL activity in hypothalamus or brain independent of diabetic and nutritional status. CONCLUSION: Thus, Angptl4 in brain is produced in glia and regulated by insulin. However, in contrast to the periphery, central Angptl4 does not regulate LPL activity, but appears to participate in the metabolic crosstalk between glia and neurons. Elsevier 2014-11-13 /pmc/articles/PMC4314546/ /pubmed/25685701 http://dx.doi.org/10.1016/j.molmet.2014.11.003 Text en © 2014 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Brief Communication Vienberg, Sara Gry Kleinridders, André Suzuki, Ryo Kahn, C. Ronald Differential effects of angiopoietin-like 4 in brain and muscle on regulation of lipoprotein lipase activity |
title | Differential effects of angiopoietin-like 4 in brain and muscle on regulation of lipoprotein lipase activity |
title_full | Differential effects of angiopoietin-like 4 in brain and muscle on regulation of lipoprotein lipase activity |
title_fullStr | Differential effects of angiopoietin-like 4 in brain and muscle on regulation of lipoprotein lipase activity |
title_full_unstemmed | Differential effects of angiopoietin-like 4 in brain and muscle on regulation of lipoprotein lipase activity |
title_short | Differential effects of angiopoietin-like 4 in brain and muscle on regulation of lipoprotein lipase activity |
title_sort | differential effects of angiopoietin-like 4 in brain and muscle on regulation of lipoprotein lipase activity |
topic | Brief Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4314546/ https://www.ncbi.nlm.nih.gov/pubmed/25685701 http://dx.doi.org/10.1016/j.molmet.2014.11.003 |
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