New aspects of the molecular constituents of tissue barriers
Epithelial and endothelial tissue barriers are based on tight intercellular contacts (Tight Junctions, TJs) between neighbouring cells. TJs are multimeric complexes, located at the most apical border of the lateral membrane. So far, a plethora of proteins locating at tight intercellular contacts hav...
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| Published in | Journal of Neural Transmission Vol. 118; no. 1; pp. 7 - 21 |
|---|---|
| Main Authors | , , , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
Vienna
Springer Vienna
01.01.2011
Springer Nature B.V |
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| Online Access | Get full text |
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| Abstract | Epithelial and endothelial tissue barriers are based on tight intercellular contacts (Tight Junctions, TJs) between neighbouring cells. TJs are multimeric complexes, located at the most apical border of the lateral membrane. So far, a plethora of proteins locating at tight intercellular contacts have been discovered, the role of which has just partly been unraveled. Yet, there is convincing evidence that many TJ proteins exert a dual role: They act as structural components at the junctional site and they are involved in signalling pathways leading to alterations of gene expression and cell behaviour (migration, proliferation). This review will shortly summarize the classical functions of TJs and TJ-related proteins and will introduce a new category, termed the “non-classical” functions of junctional proteins. A particular focus will be directed towards the nuclear targeting of junctional proteins and the downstream effects elicited by their intranuclear activities. |
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| AbstractList | Epithelial and endothelial tissue barriers are based on tight intercellular contacts (Tight Junctions, TJs) between neighbouring cells. TJs are multimeric complexes, located at the most apical border of the lateral membrane. So far, a plethora of proteins locating at tight intercellular contacts have been discovered, the role of which has just partly been unraveled. Yet, there is convincing evidence that many TJ proteins exert a dual role: They act as structural components at the junctional site and they are involved in signalling pathways leading to alterations of gene expression and cell behaviour (migration, proliferation). This review will shortly summarize the classical functions of TJs and TJ-related proteins and will introduce a new category, termed the “non-classical” functions of junctional proteins. A particular focus will be directed towards the nuclear targeting of junctional proteins and the downstream effects elicited by their intranuclear activities. Issue Title: Blood-CNS Barrier, Neurodegeneration and Neuroprotection: Recent Therapeutic Advancements and Nano-drug Delivery Epithelial and endothelial tissue barriers are based on tight intercellular contacts (Tight Junctions, TJs) between neighbouring cells. TJs are multimeric complexes, located at the most apical border of the lateral membrane. So far, a plethora of proteins locating at tight intercellular contacts have been discovered, the role of which has just partly been unraveled. Yet, there is convincing evidence that many TJ proteins exert a dual role: They act as structural components at the junctional site and they are involved in signalling pathways leading to alterations of gene expression and cell behaviour (migration, proliferation). This review will shortly summarize the classical functions of TJs and TJ-related proteins and will introduce a new category, termed the "non-classical" functions of junctional proteins. A particular focus will be directed towards the nuclear targeting of junctional proteins and the downstream effects elicited by their intranuclear activities.[PUBLICATION ABSTRACT] |
| Author | Krizbai, I. Lehner, C. Tempfer, H. Traweger, A. Wilhelm, I. Bauer, H. Bauer, H. C. Zweimueller-Mayer, J. |
| Author_xml | – sequence: 1 givenname: H. C. surname: Bauer fullname: Bauer, H. C. organization: Department of Organismic Biology, University of Salzburg, Paracelsus Private Medical University – sequence: 2 givenname: A. surname: Traweger fullname: Traweger, A. organization: Baxter Innovations GmbH – sequence: 3 givenname: J. surname: Zweimueller-Mayer fullname: Zweimueller-Mayer, J. organization: Department of Organismic Biology, University of Salzburg – sequence: 4 givenname: C. surname: Lehner fullname: Lehner, C. organization: Department of Organismic Biology, University of Salzburg, Department of Traumatology and Sports Injuries, Paracelsus Private Medical University – sequence: 5 givenname: H. surname: Tempfer fullname: Tempfer, H. organization: Paracelsus Private Medical University – sequence: 6 givenname: I. surname: Krizbai fullname: Krizbai, I. organization: Biological Research Center, Institute of Biophysics – sequence: 7 givenname: I. surname: Wilhelm fullname: Wilhelm, I. organization: Biological Research Center, Institute of Biophysics – sequence: 8 givenname: H. surname: Bauer fullname: Bauer, H. email: Hannelore.Bauer@sbg.ac.at organization: Department of Organismic Biology, University of Salzburg |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/20865434$$D View this record in MEDLINE/PubMed |
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| Keywords | Endothelia Tissue-barriers Tight junctions Epithelia |
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| Title | New aspects of the molecular constituents of tissue barriers |
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