RESUMEN
BACKGROUND: Missense mutations in keratin 5 and 14 genes cause the severe skin fragility disorder epidermolysis bullosa simplex (EBS) by collapsing of the keratin cytoskeleton into cytoplasmic protein aggregates. Despite intense efforts, no molecular therapies are available, mostly due to the complex phenotype of EBS, comprising cell fragility, diminished adhesion, skin inflammation and itch. METHODS: We extensively characterized KRT5 and KRT14 mutant keratinocytes from patients with severe generalized EBS following exposure to the chemical chaperone 4-phenylbutyrate (4-PBA). FINDINGS: 4-PBA diminished keratin aggregates within EBS cells and ameliorated their inflammatory phenotype. Chemoproteomics of 4-PBA-treated and untreated EBS cells revealed reduced IL1ß expression- but also showed activation of Wnt/ß-catenin and NF-kB pathways. The abundance of extracellular matrix and cytoskeletal proteins was significantly altered, coinciding with diminished keratinocyte adhesion and migration in a 4-PBA dose-dependent manner. INTERPRETATION: Together, our study reveals a complex interplay of benefits and disadvantages that challenge the use of 4-PBA in skin fragility disorders.
Asunto(s)
Epidermólisis Ampollosa/metabolismo , Epidermólisis Ampollosa/patología , Queratinocitos/efectos de los fármacos , Queratinocitos/metabolismo , Queratinas/metabolismo , Fenilbutiratos/farmacología , Animales , Apoptosis/genética , Biomarcadores , Biopsia , Adhesión Celular , Comunicación Celular , Línea Celular , Citoesqueleto/metabolismo , Modelos Animales de Enfermedad , Epidermólisis Ampollosa/etiología , Matriz Extracelular/metabolismo , Humanos , Inmunohistoquímica , Queratinocitos/patología , Ratones , Fenotipo , Fenilbutiratos/uso terapéutico , Transporte de Proteínas , Proteoma , Proteómica/métodos , Transducción de Señal , Piel/efectos de los fármacos , Piel/metabolismo , Piel/patologíaAsunto(s)
Vesícula/metabolismo , Citocinas/metabolismo , Dermatitis Atópica/metabolismo , Queratinas/metabolismo , Piel/metabolismo , Animales , Vesícula/genética , Citocinas/genética , Proteínas del Citoesqueleto/genética , Proteínas del Citoesqueleto/metabolismo , Dermatitis Atópica/genética , Humanos , Queratina-14/genética , Queratina-14/metabolismo , Queratina-5/genética , Queratina-5/metabolismo , Queratinas/genética , Ratones , Mutación/genética , Linfopoyetina del Estroma TímicoRESUMEN
Expression and interaction of desmosomal components and keratins provide stable cell cohesion and protect the epidermis against various types of stress. The differentiation-specific isotype composition of the keratin cytoskeleton and desmosomes is regarded as a major determinant of adhesive strength. In support, wound healing is characterized by a transient decrease in desmosomal adhesion accompanied by increased expression of keratins K6/K16/K17 at the expense of K1/K10. The significance of altered keratin expression for desmosomal composition and adhesion remains incompletely understood at a mechanistic and functional level. Here, we investigated the respective contribution of K5/K14 or K6/K17 to desmosome adhesion, on their stable re-expression in keratinocytes lacking all keratins. This revealed that K5/K14 filaments support stable desmosomes, whereas "wound healing" keratins K6/K17 induce elevated protein kinase C alpha-mediated desmosome disassembly and subsequent destabilization of epithelial sheets. Moreover, our data suggest that K5/K14 sequester protein kinase C alpha in the cytoplasm, whereas K6/K17 or the absence of all keratins enables protein kinase C alpha translocation to the plasma membrane and induction of desmosome disassembly. Gain- and loss-of-function experiments support a major role of K5 in desmosome stability control via protein kinase C alpha. Our data show that keratin isotypes differently and specifically regulate wound healing and invasion by modulating intercellular adhesion.
Asunto(s)
Diferenciación Celular/fisiología , Desmosomas/metabolismo , Queratinocitos/citología , Proteína Quinasa C-alfa/metabolismo , Cicatrización de Heridas/fisiología , Biotinilación/métodos , Western Blotting , Fraccionamiento Celular/métodos , Células Cultivadas , Citoesqueleto/metabolismo , Células Epidérmicas , Epidermis/metabolismo , Silenciador del Gen , Humanos , Queratinocitos/metabolismo , Microscopía Fluorescente , Reacción en Cadena en Tiempo Real de la Polimerasa/métodos , Sensibilidad y EspecificidadRESUMEN
Keratin filaments constitute the major component of the epidermal cytoskeleton from heterodimers of type I and type II keratin subunits. Missense mutations in keratin 5 or keratin 14, highly expressed in the basal epidermis, cause the severe skin blistering disease epidermolysis bullosa simplex (EBS) in humans by rendering the keratin cytoskeleton sensitive to mechanical stress; yet, the mechanisms by which individual mutations cause cell fragility are incompletely understood. Here, we compared the K14p.Arg125Pro with the K5p.Glu477Asp mutation, both giving rise to severe generalized EBS, by stable expression in keratin-free keratinocytes. This revealed distinctly different effects on keratin cytoskeletal organization, in agreement with in vivo observations, thus validating the cell system. Although the K14p.Arg125Pro mutation led to impaired desmosomes, downregulation of desmosomal proteins, and weakened epithelial sheet integrity upon shear stress, the K5p.Glu477Asp mutation did not impair these functions, although causing EBS with squamous cell carcinoma in vivo. Atomic force microscopy demonstrated that K14 mutant cells were even less resistant against deformation compared with keratin-free keratinocytes. Thus, a keratin mutation causing EBS compromises cell stiffness to a greater extent than the lack of keratins. Finally, re-expression of K14 in K14 mutant cells did not rescue the above defects. Collectively, our findings have implications for EBS therapy approaches.
Asunto(s)
Epidermólisis Ampollosa Simple/genética , Queratina-14/genética , Queratina-5/genética , Mutación Missense , Piel/patología , Adhesión Celular/genética , Células Cultivadas , Citoesqueleto/metabolismo , Progresión de la Enfermedad , Epidermólisis Ampollosa Simple/patología , Humanos , Filamentos Intermedios/genética , Queratinocitos/citología , Queratinocitos/metabolismo , Muestreo , Índice de Severidad de la Enfermedad , Estadísticas no ParamétricasRESUMEN
The epidermis is a stratified epithelium that relies on its cytoskeleton and cell junctions to protect the body against mechanical injury, dehydration, and infections. Keratin intermediate filament proteins are involved in many of these functions by forming cell-specific cytoskeletal scaffolds crucial for the maintenance of cell and tissue integrity. In response to various stresses, the expression and organization of keratins are altered at transcriptional and posttranslational levels to restore tissue homeostasis. Failure to restore tissue homeostasis in the presence of keratin gene mutations results in acute and chronic skin disorders for which currently no rational therapies are available. Here, we review the recent progress on the role of keratins in cytoarchitecture, adhesion, signaling, and inflammation. By focusing on epidermal keratins, we illustrate the contribution of keratin isotypes to differentiated epithelial functions.