Lipid Polarity Is Maintained in Absence of Tight Junctions
The role of tight junctions (TJs) in the establishment and maintenance of lipid polarity in epithelial cells has long been a subject of controversy. We have addressed this issue using lysenin, a toxin derived from earthworms, and an influenza virus labeled with a fluorescent lipid, octadecylrhodamin...
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Published in | The Journal of biological chemistry Vol. 287; no. 12; pp. 9525 - 9533 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Elsevier Inc
16.03.2012
American Society for Biochemistry and Molecular Biology |
Subjects | |
Online Access | Get full text |
ISSN | 0021-9258 1083-351X 1083-351X |
DOI | 10.1074/jbc.M111.327064 |
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Abstract | The role of tight junctions (TJs) in the establishment and maintenance of lipid polarity in epithelial cells has long been a subject of controversy. We have addressed this issue using lysenin, a toxin derived from earthworms, and an influenza virus labeled with a fluorescent lipid, octadecylrhodamine B (R18). When epithelial cells are stained with lysenin, lysenin selectively binds to their apical membranes. Using an artificial liposome, we demonstrated that lysenin recognizes the membrane domains where sphingomyelins are clustered. Interestingly, lysenin selectively stained the apical membranes of epithelial cells depleted of zonula occludens proteins (ZO-deficient cells), which completely lack TJs. Furthermore, the fluorescent lipid inserted into the apical membrane by fusion with the influenza virus did not diffuse to the lateral membrane in ZO-deficient epithelial cells. This study revealed that sphingomyelin-cluster formation occurs only in the apical membrane and that lipid polarity is maintained even in the absence of TJs.
Tight junctions (TJs) are thought to prevent lipids from diffusing freely between the apical and basolateral membrane.
We demonstrated that lipids from the apical and basolateral membranes are segregated in an epithelial cell line lacking ZO-proteins.
TJs are not essential for the maintenance of lipid polarity in epithelial cells.
We demonstrated that the formation of TJs and lipid polarity occurs independently in epithelial cells. |
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AbstractList | Background:
Tight junctions (TJs) are thought to prevent lipids from diffusing freely between the apical and basolateral membrane.
Results:
We demonstrated that lipids from the apical and basolateral membranes are segregated in an epithelial cell line lacking ZO-proteins.
Conclusion:
TJs are not essential for the maintenance of lipid polarity in epithelial cells.
Significance:
We demonstrated that the formation of TJs and lipid polarity occurs independently in epithelial cells.
The role of tight junctions (TJs) in the establishment and maintenance of lipid polarity in epithelial cells has long been a subject of controversy. We have addressed this issue using lysenin, a toxin derived from earthworms, and an influenza virus labeled with a fluorescent lipid, octadecylrhodamine B (R18). When epithelial cells are stained with lysenin, lysenin selectively binds to their apical membranes. Using an artificial liposome, we demonstrated that lysenin recognizes the membrane domains where sphingomyelins are clustered. Interestingly, lysenin selectively stained the apical membranes of epithelial cells depleted of zonula occludens proteins (ZO-deficient cells), which completely lack TJs. Furthermore, the fluorescent lipid inserted into the apical membrane by fusion with the influenza virus did not diffuse to the lateral membrane in ZO-deficient epithelial cells. This study revealed that sphingomyelin-cluster formation occurs only in the apical membrane and that lipid polarity is maintained even in the absence of TJs. The role of tight junctions (TJs) in the establishment and maintenance of lipid polarity in epithelial cells has long been a subject of controversy. We have addressed this issue using lysenin, a toxin derived from earthworms, and an influenza virus labeled with a fluorescent lipid, octadecylrhodamine B (R18). When epithelial cells are stained with lysenin, lysenin selectively binds to their apical membranes. Using an artificial liposome, we demonstrated that lysenin recognizes the membrane domains where sphingomyelins are clustered. Interestingly, lysenin selectively stained the apical membranes of epithelial cells depleted of zonula occludens proteins (ZO-deficient cells), which completely lack TJs. Furthermore, the fluorescent lipid inserted into the apical membrane by fusion with the influenza virus did not diffuse to the lateral membrane in ZO-deficient epithelial cells. This study revealed that sphingomyelin-cluster formation occurs only in the apical membrane and that lipid polarity is maintained even in the absence of TJs.The role of tight junctions (TJs) in the establishment and maintenance of lipid polarity in epithelial cells has long been a subject of controversy. We have addressed this issue using lysenin, a toxin derived from earthworms, and an influenza virus labeled with a fluorescent lipid, octadecylrhodamine B (R18). When epithelial cells are stained with lysenin, lysenin selectively binds to their apical membranes. Using an artificial liposome, we demonstrated that lysenin recognizes the membrane domains where sphingomyelins are clustered. Interestingly, lysenin selectively stained the apical membranes of epithelial cells depleted of zonula occludens proteins (ZO-deficient cells), which completely lack TJs. Furthermore, the fluorescent lipid inserted into the apical membrane by fusion with the influenza virus did not diffuse to the lateral membrane in ZO-deficient epithelial cells. This study revealed that sphingomyelin-cluster formation occurs only in the apical membrane and that lipid polarity is maintained even in the absence of TJs. The role of tight junctions (TJs) in the establishment and maintenance of lipid polarity in epithelial cells has long been a subject of controversy. We have addressed this issue using lysenin, a toxin derived from earthworms, and an influenza virus labeled with a fluorescent lipid, octadecylrhodamine B (R18). When epithelial cells are stained with lysenin, lysenin selectively binds to their apical membranes. Using an artificial liposome, we demonstrated that lysenin recognizes the membrane domains where sphingomyelins are clustered. Interestingly, lysenin selectively stained the apical membranes of epithelial cells depleted of zonula occludens proteins (ZO-deficient cells), which completely lack TJs. Furthermore, the fluorescent lipid inserted into the apical membrane by fusion with the influenza virus did not diffuse to the lateral membrane in ZO-deficient epithelial cells. This study revealed that sphingomyelin-cluster formation occurs only in the apical membrane and that lipid polarity is maintained even in the absence of TJs. The role of tight junctions (TJs) in the establishment and maintenance of lipid polarity in epithelial cells has long been a subject of controversy. We have addressed this issue using lysenin, a toxin derived from earthworms, and an influenza virus labeled with a fluorescent lipid, octadecylrhodamine B (R18). When epithelial cells are stained with lysenin, lysenin selectively binds to their apical membranes. Using an artificial liposome, we demonstrated that lysenin recognizes the membrane domains where sphingomyelins are clustered. Interestingly, lysenin selectively stained the apical membranes of epithelial cells depleted of zonula occludens proteins (ZO-deficient cells), which completely lack TJs. Furthermore, the fluorescent lipid inserted into the apical membrane by fusion with the influenza virus did not diffuse to the lateral membrane in ZO-deficient epithelial cells. This study revealed that sphingomyelin-cluster formation occurs only in the apical membrane and that lipid polarity is maintained even in the absence of TJs. Tight junctions (TJs) are thought to prevent lipids from diffusing freely between the apical and basolateral membrane. We demonstrated that lipids from the apical and basolateral membranes are segregated in an epithelial cell line lacking ZO-proteins. TJs are not essential for the maintenance of lipid polarity in epithelial cells. We demonstrated that the formation of TJs and lipid polarity occurs independently in epithelial cells. |
Author | Kobayashi, Toshihide Taguchi, Ryo Umeda, Masato Suzuki, Mayu Ikeda, Kazutaka Sato, Satoshi B. Stolz, Donna B. Ikenouchi, Junichi Umeda, Kazuaki Kobayashi, Tetsuyuki |
Author_xml | – sequence: 1 givenname: Junichi surname: Ikenouchi fullname: Ikenouchi, Junichi email: ikenouchi@sbchem.kyoto-u.ac.jp organization: Department of Synthetic Chemistry and Biological Chemistry, Graduate School of Engineering, Kyoto University, Kyoto 615-8510, Japan – sequence: 2 givenname: Mayu surname: Suzuki fullname: Suzuki, Mayu organization: Department of Synthetic Chemistry and Biological Chemistry, Graduate School of Engineering, Kyoto University, Kyoto 615-8510, Japan – sequence: 3 givenname: Kazuaki surname: Umeda fullname: Umeda, Kazuaki organization: Department of Molecular Pharmacology, Graduate School of Medical Sciences, Kumamoto University, 1-1-1 Honjo, Kumamoto 860-8556, Japan – sequence: 4 givenname: Kazutaka surname: Ikeda fullname: Ikeda, Kazutaka organization: Department of Metabolome, Graduate School of Medicine, The University of Tokyo, Bunkyo-ku, Tokyo 113-0033, Japan – sequence: 5 givenname: Ryo surname: Taguchi fullname: Taguchi, Ryo organization: Department of Metabolome, Graduate School of Medicine, The University of Tokyo, Bunkyo-ku, Tokyo 113-0033, Japan – sequence: 6 givenname: Tetsuyuki surname: Kobayashi fullname: Kobayashi, Tetsuyuki organization: CREST, Japan Science and Technology Agency (JST), Kawaguchi, Saitama 332-0012, Japan – sequence: 7 givenname: Satoshi B. surname: Sato fullname: Sato, Satoshi B. organization: Research Center for Low Temperature and Material Sciences, Kyoto University, Kyoto 606-8501, Japan – sequence: 8 givenname: Toshihide surname: Kobayashi fullname: Kobayashi, Toshihide organization: RIKEN, Wako, Saitama 351-0198, Japan – sequence: 9 givenname: Donna B. surname: Stolz fullname: Stolz, Donna B. organization: Department of Cell Biology and Physiology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania 15261 – sequence: 10 givenname: Masato surname: Umeda fullname: Umeda, Masato organization: Department of Synthetic Chemistry and Biological Chemistry, Graduate School of Engineering, Kyoto University, Kyoto 615-8510, Japan |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/22294698$$D View this record in MEDLINE/PubMed |
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Keywords | Membrane Structure Epithelial Polarity Tight Junctions Epithelial Cell Sphingomyelin Membrane Membrane Lipids Lysenin |
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Snippet | The role of tight junctions (TJs) in the establishment and maintenance of lipid polarity in epithelial cells has long been a subject of controversy. We have... Background: Tight junctions (TJs) are thought to prevent lipids from diffusing freely between the apical and basolateral membrane. Results: We demonstrated... |
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SubjectTerms | Cell Biology Cell Line Cell Membrane - metabolism Cell Polarity Epithelial Cell Epithelial Cells - cytology Epithelial Cells - metabolism Epithelial Polarity Humans Lysenin Membrane Membrane Lipids Membrane Structure Sphingomyelin Sphingomyelins - metabolism Tight Junctions Tight Junctions - metabolism |
Title | Lipid Polarity Is Maintained in Absence of Tight Junctions |
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