β2-adrenergic receptor regulates ER-mitochondria contacts
Abstract Interactions between the endoplasmic reticulum (ER) and mitochondria (Mito) are crucial for many cellular functions, and their interaction levels change dynamically depending on the cellular environment. Little is known about how the interactions between these organelles are regulated withi...
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Nature Portfolio
2021
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oai:doaj.org-article:78fa7932c9b64ab09ce7916196309add2021-11-08T10:46:17Zβ2-adrenergic receptor regulates ER-mitochondria contacts10.1038/s41598-021-00801-w2045-2322https://doaj.org/article/78fa7932c9b64ab09ce7916196309add2021-11-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-00801-whttps://doaj.org/toc/2045-2322Abstract Interactions between the endoplasmic reticulum (ER) and mitochondria (Mito) are crucial for many cellular functions, and their interaction levels change dynamically depending on the cellular environment. Little is known about how the interactions between these organelles are regulated within the cell. Here we screened a compound library to identify chemical modulators for ER-Mito contacts in HEK293T cells. Multiple agonists of G-protein coupled receptors (GPCRs), beta-adrenergic receptors (β-ARs) in particular, scored in this screen. Analyses in multiple orthogonal assays validated that β2-AR activation promotes physical and functional interactions between the two organelles. Furthermore, we have elucidated potential downstream effectors mediating β2-AR-induced ER-Mito contacts. Together our study identifies β2-AR signaling as an important regulatory pathway for ER-Mito coupling and highlights the role of these contacts in responding to physiological demands or stresses.Youngshin LimIl-Taeg ChoHelmut G. RennkeGinam ChoNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-16 (2021) |
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Medicine R Science Q Youngshin Lim Il-Taeg Cho Helmut G. Rennke Ginam Cho β2-adrenergic receptor regulates ER-mitochondria contacts |
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Abstract Interactions between the endoplasmic reticulum (ER) and mitochondria (Mito) are crucial for many cellular functions, and their interaction levels change dynamically depending on the cellular environment. Little is known about how the interactions between these organelles are regulated within the cell. Here we screened a compound library to identify chemical modulators for ER-Mito contacts in HEK293T cells. Multiple agonists of G-protein coupled receptors (GPCRs), beta-adrenergic receptors (β-ARs) in particular, scored in this screen. Analyses in multiple orthogonal assays validated that β2-AR activation promotes physical and functional interactions between the two organelles. Furthermore, we have elucidated potential downstream effectors mediating β2-AR-induced ER-Mito contacts. Together our study identifies β2-AR signaling as an important regulatory pathway for ER-Mito coupling and highlights the role of these contacts in responding to physiological demands or stresses. |
format |
article |
author |
Youngshin Lim Il-Taeg Cho Helmut G. Rennke Ginam Cho |
author_facet |
Youngshin Lim Il-Taeg Cho Helmut G. Rennke Ginam Cho |
author_sort |
Youngshin Lim |
title |
β2-adrenergic receptor regulates ER-mitochondria contacts |
title_short |
β2-adrenergic receptor regulates ER-mitochondria contacts |
title_full |
β2-adrenergic receptor regulates ER-mitochondria contacts |
title_fullStr |
β2-adrenergic receptor regulates ER-mitochondria contacts |
title_full_unstemmed |
β2-adrenergic receptor regulates ER-mitochondria contacts |
title_sort |
β2-adrenergic receptor regulates er-mitochondria contacts |
publisher |
Nature Portfolio |
publishDate |
2021 |
url |
https://doaj.org/article/78fa7932c9b64ab09ce7916196309add |
work_keys_str_mv |
AT youngshinlim b2adrenergicreceptorregulatesermitochondriacontacts AT iltaegcho b2adrenergicreceptorregulatesermitochondriacontacts AT helmutgrennke b2adrenergicreceptorregulatesermitochondriacontacts AT ginamcho b2adrenergicreceptorregulatesermitochondriacontacts |
_version_ |
1718442630045499392 |