Keratins Regulate the Adhesive Properties of Desmosomal Cadherins through Signaling

被引:39
|
作者
Vielmuth, Franziska [1 ]
Wanuske, Marie-Theres [1 ]
Radeva, Mariya Y. [1 ]
Hiermaier, Matthias [1 ]
Kugelmann, Daniela [1 ]
Walter, Elias [1 ]
Buechau, Fanny [2 ,3 ]
Magin, Thomas M. [2 ,3 ]
Waschke, Jens [1 ]
Spindler, Volker [1 ]
机构
[1] Ludwig Maximilians Univ Munchen, Inst Anat, Fac Med, Pettenkoferstr 11, D-80336 Munich, Germany
[2] Univ Leipzig, Inst Biol, Leipzig, Germany
[3] Univ Leipzig, Translat Ctr Regenerat Med, Sachsischer Inkubator Klin Translat, Leipzig, Germany
关键词
PEMPHIGUS-VULGARIS-IGG; CELL-CELL ADHESION; DESMOGLEIN; 3; FORCE SPECTROSCOPY; CULTURED KERATINOCYTES; PKC-ALPHA; MICROSCOPY; DYNAMICS; DISSOCIATION; COHESION;
D O I
10.1016/j.jid.2017.08.033
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Tightly controlled intercellular adhesion is crucial for the integrity and function of the epidermis. The keratin filament cytoskeleton anchors desmosomes, supramolecular complexes required for strong intercellular adhesion. We tested whether keratin filaments control cell adhesion by regulating the adhesive properties of desmosomal cadherins such as desmoglein (Dsg) 3. Atomic force microscopy and fluorescence recovery after photobleaching experiments showed reduced Dsg3 adhesive forces and membrane stability in murine keratinocytes lacking all keratin filaments. Impairment of the actin cytoskeleton also resulted in decreased Dsg3 immobilization but did not affect Dsg3 binding properties, indicating that the latter are exclusively controlled by keratins. Reduced binding forces were dependent on p38 mitogen-activated protein kinase activity, which was deregulated in keratin-deficient cells. In contrast, inhibition of protein kinase C signaling, which is known to be controlled by keratins, promoted and spatially stabilized Dsg3-mediated interactions in the membrane. These results show a previously unreported mechanism for how keratins stabilize intercellular adhesion on the level of single desmosomal adhesion molecules.
引用
收藏
页码:121 / 131
页数:11
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