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Cortical actin contributes to spatial organization of ER-PM junctions
Endoplasmic reticulum-plasma membrane (ER-PM) junctions mediate crucial activities ranging from Ca signaling to lipid metabolism. Spatial organization of ER-PM junctions may modulate the extent and location of these cellular activities. However, the morphology and distribution of ER-PM junctions are...
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Published in: | Molecular biology of the cell 2017-11, Vol.28 (23), p.3171-3180 |
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creator | Hsieh, Ting-Sung Chen, Yu-Ju Chang, Chi-Lun Lee, Wan-Ru Liou, Jen |
description | Endoplasmic reticulum-plasma membrane (ER-PM) junctions mediate crucial activities ranging from Ca
signaling to lipid metabolism. Spatial organization of ER-PM junctions may modulate the extent and location of these cellular activities. However, the morphology and distribution of ER-PM junctions are not well characterized. Using photoactivated localization microscopy, we reveal that the contact area of single ER-PM junctions is mainly oblong with the dimensions of ∼120 nm × ∼80 nm in HeLa cells. Using total internal reflection fluorescence microscopy and structure illumination microscopy, we show that cortical actin contributes to spatial distribution and stability of ER-PM junctions. Further functional assays suggest that intact F-actin architecture is required for phosphatidylinositol 4,5-bisphosphate homeostasis mediated by Nir2 at ER-PM junctions. Together, our study provides quantitative information on spatial organization of ER-PM junctions that is in part regulated by F-actin. We envision that functions of ER-PM junctions can be differentially regulated through dynamic actin remodeling during cellular processes. |
doi_str_mv | 10.1091/mbc.E17-06-0377 |
format | article |
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signaling to lipid metabolism. Spatial organization of ER-PM junctions may modulate the extent and location of these cellular activities. However, the morphology and distribution of ER-PM junctions are not well characterized. Using photoactivated localization microscopy, we reveal that the contact area of single ER-PM junctions is mainly oblong with the dimensions of ∼120 nm × ∼80 nm in HeLa cells. Using total internal reflection fluorescence microscopy and structure illumination microscopy, we show that cortical actin contributes to spatial distribution and stability of ER-PM junctions. Further functional assays suggest that intact F-actin architecture is required for phosphatidylinositol 4,5-bisphosphate homeostasis mediated by Nir2 at ER-PM junctions. Together, our study provides quantitative information on spatial organization of ER-PM junctions that is in part regulated by F-actin. We envision that functions of ER-PM junctions can be differentially regulated through dynamic actin remodeling during cellular processes.</description><identifier>ISSN: 1059-1524</identifier><identifier>EISSN: 1939-4586</identifier><identifier>DOI: 10.1091/mbc.E17-06-0377</identifier><identifier>PMID: 28954864</identifier><language>eng</language><publisher>United States: The American Society for Cell Biology</publisher><subject>Actin Cytoskeleton - metabolism ; Actins - metabolism ; Brief Reports ; Calcium - metabolism ; Cell Membrane - metabolism ; Endoplasmic Reticulum - metabolism ; Endoplasmic Reticulum - physiology ; HeLa Cells ; Homeostasis ; Humans ; Membrane Proteins - metabolism ; Phosphatidylinositols - metabolism ; Signal Transduction ; Spatial Analysis</subject><ispartof>Molecular biology of the cell, 2017-11, Vol.28 (23), p.3171-3180</ispartof><rights>2017 Hsieh et al. This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License (http://creativecommons.org/licenses/by-nc-sa/3.0).</rights><rights>2017 Hsieh This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License ( ). 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c439t-2a7b4805649913c88d8dc8c5218420f2fed7337e18ffe268af4d0c7ca240549d3</citedby><cites>FETCH-LOGICAL-c439t-2a7b4805649913c88d8dc8c5218420f2fed7337e18ffe268af4d0c7ca240549d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5687020/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5687020/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28954864$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Lippincott-Schwartz, Jennifer</contributor><creatorcontrib>Hsieh, Ting-Sung</creatorcontrib><creatorcontrib>Chen, Yu-Ju</creatorcontrib><creatorcontrib>Chang, Chi-Lun</creatorcontrib><creatorcontrib>Lee, Wan-Ru</creatorcontrib><creatorcontrib>Liou, Jen</creatorcontrib><title>Cortical actin contributes to spatial organization of ER-PM junctions</title><title>Molecular biology of the cell</title><addtitle>Mol Biol Cell</addtitle><description>Endoplasmic reticulum-plasma membrane (ER-PM) junctions mediate crucial activities ranging from Ca
signaling to lipid metabolism. Spatial organization of ER-PM junctions may modulate the extent and location of these cellular activities. However, the morphology and distribution of ER-PM junctions are not well characterized. Using photoactivated localization microscopy, we reveal that the contact area of single ER-PM junctions is mainly oblong with the dimensions of ∼120 nm × ∼80 nm in HeLa cells. Using total internal reflection fluorescence microscopy and structure illumination microscopy, we show that cortical actin contributes to spatial distribution and stability of ER-PM junctions. Further functional assays suggest that intact F-actin architecture is required for phosphatidylinositol 4,5-bisphosphate homeostasis mediated by Nir2 at ER-PM junctions. Together, our study provides quantitative information on spatial organization of ER-PM junctions that is in part regulated by F-actin. 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subjects | Actin Cytoskeleton - metabolism Actins - metabolism Brief Reports Calcium - metabolism Cell Membrane - metabolism Endoplasmic Reticulum - metabolism Endoplasmic Reticulum - physiology HeLa Cells Homeostasis Humans Membrane Proteins - metabolism Phosphatidylinositols - metabolism Signal Transduction Spatial Analysis |
title | Cortical actin contributes to spatial organization of ER-PM junctions |
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