Home > Publications database > Laminin-5-deficient human keratinocytes: Defective adhesion results in a saltatory and inefficient mode of migration > print |
001 | 59197 | ||
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024 | 7 | _ | |2 pmid |a pmid:17335805 |
024 | 7 | _ | |2 DOI |a 10.1016/j.yexcr.2007.02.003 |
024 | 7 | _ | |2 WOS |a WOS:000246128300006 |
037 | _ | _ | |a PreJuSER-59197 |
041 | _ | _ | |a eng |
082 | _ | _ | |a 570 |
084 | _ | _ | |2 WoS |a Oncology |
084 | _ | _ | |2 WoS |a Cell Biology |
100 | 1 | _ | |a Hartwig, B. |b 0 |0 P:(DE-HGF)0 |
245 | _ | _ | |a Laminin-5-deficient human keratinocytes: Defective adhesion results in a saltatory and inefficient mode of migration |
260 | _ | _ | |a Orlando, Fla. |b Academic Press |c 2007 |
300 | _ | _ | |a 1575 - 1587 |
336 | 7 | _ | |a Journal Article |0 PUB:(DE-HGF)16 |2 PUB:(DE-HGF) |
336 | 7 | _ | |a Output Types/Journal article |2 DataCite |
336 | 7 | _ | |a Journal Article |0 0 |2 EndNote |
336 | 7 | _ | |a ARTICLE |2 BibTeX |
336 | 7 | _ | |a JOURNAL_ARTICLE |2 ORCID |
336 | 7 | _ | |a article |2 DRIVER |
440 | _ | 0 | |a Experimental Cell Research |x 0014-4827 |0 13781 |y 8 |v 313 |
500 | _ | _ | |a Record converted from VDB: 12.11.2012 |
520 | _ | _ | |a Laminin-5 is a major adhesion protein of the skin basement membrane and crucially involved in integrin-mediated cell substrate attachment of keratinocytes, which is important for hemidesmosomal anchorage as well as for keratinocyte migration during epidermal wound healing. To investigate its role in keratinocyte migration, we analyzed laminin-5-deficient cells of patients with a lethal variant of junctional epidermolysis bullosa. Normal migrating keratinocytes adopted monopolar morphology with a distinct front lamella and employed a continuous mode of translocation. In contrast, laminin-5-deficient cells assumed a stretched bipolar shape with two lamella regions and migrated in a discontinuous, saltatory manner characterized by significantly decreased directional persistence and reduced migration velocity. The distinct morphology as well as the migratory phenotype apparently resulted from a defect in the formation of cell substrate adhesions that were completely missing in the cell body and less stable in the lamella regions. Accordingly in normal keratinocytes, a bipolar shape and a saltatory migration mode were inducible by blocking laminin-5-mediated substrate adhesion. Our findings clearly point to an essential role of laminin-5 in forming dynamic cell substrate adhesion during migration of epidermal keratinocytes and provide an explanation for the cellular mechanisms that underlie the lethal form of junctional epidermolysis bullosa. |
536 | _ | _ | |a Kondensierte Materie |c P54 |2 G:(DE-HGF) |0 G:(DE-Juel1)FUEK414 |x 0 |
588 | _ | _ | |a Dataset connected to Web of Science, Pubmed |
650 | _ | 2 | |2 MeSH |a Cell Adhesion |
650 | _ | 2 | |2 MeSH |a Cell Adhesion Molecules: genetics |
650 | _ | 2 | |2 MeSH |a Cell Adhesion Molecules: metabolism |
650 | _ | 2 | |2 MeSH |a Cell Adhesion Molecules: physiology |
650 | _ | 2 | |2 MeSH |a Cell Movement |
650 | _ | 2 | |2 MeSH |a Cell Polarity |
650 | _ | 2 | |2 MeSH |a Cell Shape |
650 | _ | 2 | |2 MeSH |a Cells, Cultured |
650 | _ | 2 | |2 MeSH |a Epidermolysis Bullosa, Junctional: metabolism |
650 | _ | 2 | |2 MeSH |a Epidermolysis Bullosa, Junctional: pathology |
650 | _ | 2 | |2 MeSH |a Extracellular Matrix Proteins: metabolism |
650 | _ | 2 | |2 MeSH |a Humans |
650 | _ | 2 | |2 MeSH |a Keratinocytes: physiology |
650 | _ | 2 | |2 MeSH |a Pseudopodia: physiology |
650 | _ | 7 | |0 0 |2 NLM Chemicals |a Cell Adhesion Molecules |
650 | _ | 7 | |0 0 |2 NLM Chemicals |a Extracellular Matrix Proteins |
650 | _ | 7 | |0 0 |2 NLM Chemicals |a kalinin |
650 | _ | 7 | |a J |2 WoSType |
653 | 2 | 0 | |2 Author |a keratinocytes |
653 | 2 | 0 | |2 Author |a laminin-5-deficiency |
653 | 2 | 0 | |2 Author |a junctional epidermolysis bullosa |
653 | 2 | 0 | |2 Author |a cell adhesion |
653 | 2 | 0 | |2 Author |a cell migration |
653 | 2 | 0 | |2 Author |a saltatory migration |
700 | 1 | _ | |a Borm, B. |b 1 |u FZJ |0 P:(DE-Juel1)VDB57504 |
700 | 1 | _ | |a Schneider, H. |b 2 |0 P:(DE-HGF)0 |
700 | 1 | _ | |a Arin, M. J. |b 3 |0 P:(DE-HGF)0 |
700 | 1 | _ | |a Kirfel, G. |b 4 |0 P:(DE-HGF)0 |
700 | 1 | _ | |a Herzog, V. |b 5 |0 P:(DE-HGF)0 |
773 | _ | _ | |a 10.1016/j.yexcr.2007.02.003 |g Vol. 313, p. 1575 - 1587 |p 1575 - 1587 |q 313<1575 - 1587 |0 PERI:(DE-600)1466780-0 |t Experimental cell research |v 313 |y 2007 |x 0014-4827 |
856 | 7 | _ | |u http://dx.doi.org/10.1016/j.yexcr.2007.02.003 |
909 | C | O | |o oai:juser.fz-juelich.de:59197 |p VDB |
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914 | 1 | _ | |y 2007 |
915 | _ | _ | |0 StatID:(DE-HGF)0010 |a JCR/ISI refereed |
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981 | _ | _ | |a I:(DE-Juel1)ICS-7-20110106 |
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