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 inThe Journal of biological chemistry Vol. 287; no. 12; pp. 9525 - 9533
Main Authors Ikenouchi, Junichi, Suzuki, Mayu, Umeda, Kazuaki, Ikeda, Kazutaka, Taguchi, Ryo, Kobayashi, Tetsuyuki, Sato, Satoshi B., Kobayashi, Toshihide, Stolz, Donna B., Umeda, Masato
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 16.03.2012
American Society for Biochemistry and Molecular Biology
Subjects
Online AccessGet full text
ISSN0021-9258
1083-351X
1083-351X
DOI10.1074/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.
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
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Issue 12
Keywords Membrane Structure
Epithelial Polarity
Tight Junctions
Epithelial Cell
Sphingomyelin
Membrane
Membrane Lipids
Lysenin
Language English
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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
URI https://dx.doi.org/10.1074/jbc.M111.327064
https://www.ncbi.nlm.nih.gov/pubmed/22294698
https://www.proquest.com/docview/929120567
https://pubmed.ncbi.nlm.nih.gov/PMC3308754
Volume 287
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