RESUMEN

The corneocyte lipid envelope, composed of covalently bound ceramides and fatty acids, is important to the integrity of the permeability barrier in the stratum corneum, and its absence is a prime structural defect in various skin diseases associated with defective skin barrier function. SDR9C7 encodes a short-chain dehydrogenase/reductase family 9C member 7 (SDR9C7) recently found mutated in ichthyosis. In a patient with SDR9C7 mutation and a mouse Sdr9c7-KO model, we show loss of covalent binding of epidermal ceramides to protein, a structural fault in the barrier. For reasons unresolved, protein binding requires lipoxygenase-catalyzed transformations of linoleic acid (18:2) esterified in ω-O-acylceramides. In Sdr9c7-/- epidermis, quantitative liquid chromatography-mass spectometry (LC-MS) assays revealed almost complete loss of a species of ω-O-acylceramide esterified with linoleate-9,10-trans-epoxy-11E-13-ketone; other acylceramides related to the lipoxygenase pathway were in higher abundance. Recombinant SDR9C7 catalyzed NAD+-dependent dehydrogenation of linoleate 9,10-trans-epoxy-11E-13-alcohol to the corresponding 13-ketone, while ichthyosis mutants were inactive. We propose, therefore, that the critical requirement for lipoxygenases and SDR9C7 is in producing acylceramide containing the 9,10-epoxy-11E-13-ketone, a reactive moiety known for its nonenzymatic coupling to protein. This suggests a mechanism for coupling of ceramide to protein and provides important insights into skin barrier formation and pathogenesis.

Asunto(s)

Ceramidas/metabolismo , Epidermis/enzimología , Oxidorreductasas/metabolismo , Animales , Catálisis , Ceramidas/genética , Modelos Animales de Enfermedad , Enfermedades Genéticas Congénitas/enzimología , Enfermedades Genéticas Congénitas/genética , Humanos , Ictiosis/enzimología , Ictiosis/genética , Ratones , Ratones Noqueados , Oxidorreductasas/genética

Asunto(s)

Genes Recesivos , Glucosiltransferasas/genética , Ictiosis/enzimología , Ictiosis/genética , Secuencia de Bases , Resultado Fatal , Glucosiltransferasas/metabolismo , Humanos , Recién Nacido , Masculino

RESUMEN

Ichthyoses are a heterogeneous group of inherited cornification disorders characterized by generalized dry skin, scaling and/or hyperkeratosis. Ichthyosis vulgaris is the most common form of ichthyosis in humans and caused by genetic variants in the FLG gene encoding filaggrin. Filaggrin is a key player in the formation of the stratum corneum, the uppermost layer of the epidermis and therefore crucial for barrier function. During terminal differentiation of keratinocytes, the precursor profilaggrin is cleaved by several proteases into filaggrin monomers and eventually processed into free amino acids contributing to the hydration of the cornified layer. We studied a German Shepherd dog with a novel form of ichthyosis. Comparing the genome sequence of the affected dog with 288 genomes from genetically diverse non-affected dogs we identified a private heterozygous variant in the ASPRV1 gene encoding "aspartic peptidase, retroviral-like 1", which is also known as skin aspartic protease (SASPase). The variant was absent in both parents and therefore due to a de novo mutation event. It was a missense variant, c.1052T>C, affecting a conserved residue close to an autoprocessing cleavage site, p.(Leu351Pro). ASPRV1 encodes a retroviral-like protease involved in profilaggrin-to-filaggrin processing. By immunofluorescence staining we showed that the filaggrin expression pattern was altered in the affected dog. Thus, our findings provide strong evidence that the identified de novo variant is causative for the ichthyosis in the affected dog and that ASPRV1 plays an essential role in skin barrier formation. ASPRV1 is thus a novel candidate gene for unexplained human forms of ichthyoses.

Asunto(s)

Ácido Aspártico Endopeptidasas/genética , Enfermedades de los Perros/genética , Predisposición Genética a la Enfermedad/genética , Ictiosis/genética , Mutación Missense , Secuencia de Aminoácidos , Animales , Ácido Aspártico Endopeptidasas/metabolismo , Secuencia de Bases , Modelos Animales de Enfermedad , Enfermedades de los Perros/enzimología , Perros , Femenino , Proteínas Filagrina , Humanos , Ictiosis/enzimología , Ictiosis/veterinaria , Proteínas de Filamentos Intermediarios/metabolismo , Microscopía Fluorescente , Análisis de Secuencia de ADN/métodos , Homología de Secuencia de Aminoácido , Piel/enzimología , Piel/metabolismo , Piel/patología

RESUMEN

Autosomal recessive congenital ichthyosis (ARCI) is a heterogeneous group of hereditary skin disorder characterized by an aberrant cornification of the epidermis. ARCI is classified into a total of 11 subtypes (ARCI1-ARCI11) based on their causative genes or loci. Of these, the causative gene for only ARCI7 has not been identified, while it was previously mapped on chromosome 12p11.2-q13.1. In this study, we performed genetic analyses for three Lebanese families with ARCI, and successfully determined the linkage interval to 9.47 Mb region on chromosome 12q13.13-q14.1, which was unexpectedly outside of the ARCI7 locus. Whole-exome sequencing and the subsequent Sanger sequencing led to the identification of missense mutations in short chain dehydrogenase/reductase family 9C, member 7 (SDR9C7) gene on chromosome 12q13.3, i.e. two families shared an identical homozygous mutation c.599T > C (p.Ile200Thr) and one family had another homozygous mutation c.214C > T (p.Arg72Trp). In cultured cells, expression of both the mutant SDR9C7 proteins was markedly reduced as compared to wild-type protein, suggesting that the mutations severely affected a stability of the protein. In normal human skin, the SDR9C7 was abundantly expressed in granular and cornified layers of the epidermis. By contrast, in a patient's skin, its expression in the cornified layer was significantly decreased. It has previously been reported that SDR9C7 is an enzyme to convert retinal into retinol. Therefore, our study not only adds a new gene responsible for ARCI, but also further suggests a potential role of vitamin A metabolism in terminal differentiation of the epidermis in humans.

Asunto(s)

Expresión Génica , Ictiosis/enzimología , Mutación Missense , Oxidorreductasas/genética , Piel/enzimología , Adolescente , Niño , Análisis Mutacional de ADN , Femenino , Humanos , Ictiosis/genética , Líbano , Masculino , Oxidorreductasas/metabolismo , Linaje , Vitamina A/metabolismo , Adulto Joven

RESUMEN

Lipoxygenases (LOXs) are dioxygenases that catalyze the formation of corresponding hydroperoxides from polyunsaturated fatty acids such as linoleic acid and arachidonic acid. LOX enzymes are expressed in immune, epithelial, and tumor cells that display a variety of physiological functions, including inflammation, skin disorder, and tumorigenesis. In the humans and mice, six LOX isoforms have been known. 15-LOX, a prototypical enzyme originally found in reticulocytes shares the similarity of amino acid sequence as well as the biochemical property to plant LOX enzymes. 15-LOX-2, which is expressed in epithelial cells and leukocytes, has different substrate specificity in the humans and mice, therefore, the role of them in mammals has not been established. 12-LOX is an isoform expressed in epithelial cells and myeloid cells including platelets. Many mutations in this isoform are found in epithelial cancers, suggesting a potential link between 12-LOX and tumorigenesis. 12R-LOX can be found in the epithelial cells of the skin. Defects in this gene result in ichthyosis, a cutaneous disorder characterized by pathophysiologically dried skin due to abnormal loss of water from its epithelial cell layer. Similarly, eLOX-3, which is also expressed in the skin epithelial cells acting downstream 12R-LOX, is another causative factor for ichthyosis. 5-LOX is a distinct isoform playing an important role in asthma and inflammation. This isoform causes the constriction of bronchioles in response to cysteinyl leukotrienes such as LTC4, thus leading to asthma. It also induces neutrophilic inflammation by its recruitment in response to LTB4. Importantly, 5-LOX activity is strictly regulated by 5-LOX activating protein (FLAP) though the distribution of 5-LOX in the nucleus. Currently, pharmacological drugs targeting FLAP are actively developing. This review summarized these functions of LOX enzymes under pathophysiological conditions in mammals.

Asunto(s)

Proteínas Activadoras de la 5-Lipooxigenasa/genética , Antiasmáticos/uso terapéutico , Asma/tratamiento farmacológico , Asma/enzimología , Indoles/uso terapéutico , Ácidos Pentanoicos/uso terapéutico , Proteínas Activadoras de la 5-Lipooxigenasa/metabolismo , Animales , Araquidonato 12-Lipooxigenasa/genética , Araquidonato 12-Lipooxigenasa/metabolismo , Araquidonato 15-Lipooxigenasa/genética , Araquidonato 15-Lipooxigenasa/metabolismo , Asma/genética , Asma/patología , Ensayos Clínicos como Asunto , Expresión Génica , Humanos , Ictiosis/tratamiento farmacológico , Ictiosis/enzimología , Ictiosis/genética , Ictiosis/patología , Lipooxigenasa/genética , Lipooxigenasa/metabolismo , Ratones , Neoplasias/tratamiento farmacológico , Neoplasias/enzimología , Neoplasias/genética , Neoplasias/patología

RESUMEN

To explore the usefulness of protein profiling for characterization of ichthyoses, we here determined the profile of human epidermal stratum corneum by shotgun proteomics. Samples were analyzed after collection on tape circles from six anatomic sites (forearm, palm, lower leg, forehead, abdomen, upper back), demonstrating site-specific differences in profiles. Additional samples were collected from the forearms of subjects with ichthyosis vulgaris (filaggrin (FLG) deficiency), recessive X-linked ichthyosis (steroid sulfatase (STS) deficiency) and autosomal recessive congenital ichthyosis type lamellar ichthyosis (transglutaminase 1 (TGM1) deficiency). The ichthyosis protein expression patterns were readily distinguishable from each other and from phenotypically normal epidermis. In general, the degree of departure from normal was lower from ichthyosis vulgaris than from lamellar ichthyosis, parallel to the severity of the phenotype. Analysis of samples from families with ichthyosis vulgaris and concomitant modifying gene mutations (STS deficiency, GJB2 deficiency) permitted correlation of alterations in protein profile with more complex genetic constellations.

Asunto(s)

Perfilación de la Expresión Génica/métodos , Ictiosis/metabolismo , Adolescente , Adulto , Anciano , Conexina 26 , Conexinas/genética , Conexinas/metabolismo , Femenino , Proteínas Filagrina , Humanos , Ictiosis/enzimología , Ictiosis/genética , Ictiosis Vulgar/enzimología , Ictiosis Vulgar/genética , Ictiosis Vulgar/metabolismo , Masculino , Persona de Mediana Edad , Mutación , Esteril-Sulfatasa/genética , Esteril-Sulfatasa/metabolismo , Transglutaminasas/genética , Transglutaminasas/metabolismo , Adulto Joven

RESUMEN

The site-2 protease (S2P) is an unusually-hydrophobic integral membrane protease. It cleaves its substrates, which are membrane-bound transcription factors, within membrane-spanning helices. Although structural information for S2P from animals is lacking, the available data suggest that cleavage may occur at or within the lipid bilayer. In mammalian cells, S2P is essential owing to its activation of the sterol regulatory element binding proteins (SREBPs); in the absence of exogenous lipid, cells lacking S2P cannot survive. S2P is also important in the endoplasmic reticulum (ER) stress response, activating several different membrane-bound transcription factors. Human patients harboring reduction-of-function mutations in S2P exhibit an array of pathologies ranging from skin defects to neurological abnormalities. Surprisingly, Drosophila melanogaster lacking S2P are viable and fertile. This article is part of a Special Issue entitled: Intramembrane Proteases.

Asunto(s)

Proteínas de la Membrana/química , Metaloendopeptidasas/química , Transducción de Señal , Proteínas de Unión a los Elementos Reguladores de Esteroles/metabolismo , Alopecia/enzimología , Alopecia/genética , Alopecia/patología , Animales , Drosophila melanogaster/enzimología , Drosophila melanogaster/genética , Estrés del Retículo Endoplásmico/genética , Enfermedades Genéticas Ligadas al Cromosoma X/enzimología , Enfermedades Genéticas Ligadas al Cromosoma X/genética , Enfermedades Genéticas Ligadas al Cromosoma X/patología , Humanos , Ictiosis/enzimología , Ictiosis/genética , Ictiosis/patología , Metabolismo de los Lípidos , Proteínas de la Membrana/genética , Proteínas de la Membrana/metabolismo , Metaloendopeptidasas/genética , Metaloendopeptidasas/metabolismo , Mutación , Fotofobia/enzimología , Fotofobia/genética , Fotofobia/patología , Enfermedades Cutáneas Genéticas/enzimología , Enfermedades Cutáneas Genéticas/genética , Enfermedades Cutáneas Genéticas/patología , Esteroles/metabolismo , Especificidad por Sustrato

RESUMEN

Autosomal-recessive congenital ichthyoses represent a large and heterogeneous group of disorders of epidermal cornification. Recent data suggest that most of these disorders might result from defective lipid transport and metabolism. In the present study, we describe a late-onset form of recessive ichthyosis in a large consanguineous pedigree. By using a combination of homozygosity mapping and positional candidate-gene screening, we identified a 2 bp deletion in LIPN that segregated with the disease phenotype throughout the family. LIPN encodes one of six acid lipases known to be involved in triglyceride metabolism in mammals . LIPN was found to be exclusively expressed in the epidermis and to be strongly induced during keratinocyte differentiation.

Asunto(s)

Ictiosis/enzimología , Ictiosis/genética , Lipasa/genética , Eliminación de Secuencia , Adolescente , Secuencia de Bases , Consanguinidad , Cartilla de ADN/genética , Femenino , Genes Recesivos , Haplotipos , Homocigoto , Humanos , Ictiosis/patología , Masculino , Linaje , Reacción en Cadena de la Polimerasa , Polimorfismo de Longitud del Fragmento de Restricción

RESUMEN

Type I transglutaminase (TG1) is an enzyme that is responsible for assembly of the keratinocyte cornified envelope. Although TG1 mutation is an underlying cause of autosomal recessive congenital ichthyosis, a debilitating skin disease, the pathogenic mechanism is not completely understood. In the present study we show that TG1 is an endoplasmic reticulum (ER) membrane-associated protein that is trafficked through the ER for ultimate delivery to the plasma membrane. Mutation severely attenuates this processing and a catalytically inactive point mutant, TG1-FLAG(C377A), accumulates in the endoplasmic reticulum and in aggresome-like structures where it is ubiquitinylated. This accumulation results from protein misfolding, as treatment with a chemical chaperone permits it to exit the endoplasmic reticulum and travel to the plasma membrane. ER accumulation is also observed for ichthyosis-associated TG1 mutants. Our findings suggest that misfolding of TG1 mutants leads to ubiquitinylation and accumulation in the ER and aggresomes, and that abnormal intracellular processing of TG1 mutants may be an underlying cause of ichthyosis.

Asunto(s)

Membrana Celular/enzimología , Retículo Endoplásmico/enzimología , Enfermedades Genéticas Congénitas/enzimología , Ictiosis/enzimología , Queratinocitos/enzimología , Mutación Puntual , Pliegue de Proteína , Transglutaminasas/metabolismo , Ubiquitinación/genética , Membrana Celular/genética , Células Cultivadas , Retículo Endoplásmico/genética , Enfermedades Genéticas Congénitas/genética , Humanos , Ictiosis/genética , Masculino , Transporte de Proteínas/genética , Transglutaminasas/genética

RESUMEN

cgi-58 (comparative gene identification-58) is a member of alpha/beta-hydrolase family of proteins. Mutations in CGI-58 are shown to be responsible for a rare genetic disorder known as Chanarin-Dorfman syndrome, characterized by an excessive accumulation of triacylglycerol in several tissues and ichthyosis. We have earlier reported that YLR099c encoding Ict1p in Saccharomyces cerevisiae can acylate lysophosphatidic acid to phosphatidic acid. Here we report that human CGI-58 is closely related to ICT1. To understand the biochemical function of cgi-58, the gene was overexpressed in Escherichia coli, and the purified recombinant protein was found to specifically acylate lysophosphatidic acid in an acyl-CoA-dependent manner. Overexpression of CGI-58 in S. cerevisiae showed an increase in the formation of phosphatidic acid resulting in an overall increase in the total phospholipids. However, the triacylglycerol level was found to be significantly reduced. In addition, the physiological significance of cgi-58 in mice white adipose tissue was studied. We found soluble lysophosphatidic acid acyltransferase activity in mouse white adipose tissue. Immunoblot analysis using anti-Ict1p antibodies followed by mass spectrometry of the immunocross-reactive protein in lipid droplets revealed its identity as cgi-58. These observations suggest the existence of an alternate cytosolic phosphatidic acid biosynthetic pathway in the white adipose tissue. Collectively, these results reveal the role of cgi-58 as an acyltransferase.

Asunto(s)

Esterasas/metabolismo , Ictiosis/enzimología , Lipasa/metabolismo , Errores Innatos del Metabolismo Lipídico/enzimología , Lisofosfolípidos/metabolismo , Triglicéridos/metabolismo , 1-Acilglicerol-3-Fosfato O-Aciltransferasa , Acilación , Tejido Adiposo Blanco/enzimología , Animales , Esterasas/genética , Expresión Génica , Humanos , Ictiosis/metabolismo , Lipasa/genética , Errores Innatos del Metabolismo Lipídico/genética , Lisofosfolípidos/genética , Ratones , Mutación , Proteínas Recombinantes/genética , Proteínas Recombinantes/metabolismo , Saccharomyces cerevisiae/enzimología , Saccharomyces cerevisiae/genética , Proteínas de Saccharomyces cerevisiae/genética , Proteínas de Saccharomyces cerevisiae/metabolismo , Síndrome , Triglicéridos/genética

Asunto(s)

Caspasa 1/análisis , Dermatitis Atópica/enzimología , Epidermis/enzimología , Enfermedades del Cabello/enzimología , Ictiosis/enzimología , Interleucina-18/sangre , Adulto , Dermatitis Atópica/sangre , Femenino , Enfermedades del Cabello/sangre , Humanos , Ictiosis/sangre , Masculino , Síndrome

RESUMEN

Ichthyosis is a heterogeneous group of keratinization disorders reported both in human and animals. Two rare, inherited forms have been reported in cattle, both characterized by autosomal recessive transmission. Because mutations of transglutaminase 1 (TGM1) gene are associated with autosomal recessive ichthyosis in people, this gene was investigated as a candidate for the diseases in cattle. Three different polymorphisms were identified in 5' end region of cattle TGM1. Marker homozygosity was not found among affected calves. Linkage analysis excluded (logarithmic odds [LOD] score -2.0) TGM1 as the cause for ichthyosis phenotype in the analyzed Chianina cases.

Asunto(s)

Ictiosis/enzimología , Ictiosis/genética , Transglutaminasas/química , Transglutaminasas/genética , Animales , Bovinos , Ligamiento Genético , Humanos , Mutación , Polimorfismo Genético

RESUMEN

Human autosomal recessive ichthyosis with hypotrichosis (ARIH) is an inherited disorder recently linked to homozygosity for a point mutation in the ST14 gene that causes a G827R mutation in the matriptase serine protease domain (G216 in chymotrypsin numbering). Here we show that human G827R matriptase has strongly reduced proteolytic activity toward small molecule substrates, as well as toward its candidate epidermal target, prostasin. To further investigate the possible contribution of low matriptase activity to ARIH, we generated an ST14 hypomorphic mouse strain that displays a 100-fold reduction in epidermal matriptase mRNA levels. Interestingly, unlike ST14 null mice, ST14 hypomorphic mice were viable and fertile but displayed a spectrum of abnormalities that strikingly resembled ARIH. Thus, ST14 hypomorphic mice developed hyperproliferative and retention ichthyosis with impaired desquamation, hypotrichosis with brittle, thin, uneven, and sparse hair, and tooth defects. Biochemical analysis of ST14 hypomorphic epidermis revealed reduced prostasin proteolytic activation and profilaggrin proteolytic processing, compatible with a primary role of matriptase in this process. This work strongly indicates that reduced activity of a matriptase-prostasin proteolytic cascade is the etiological origin of human ARIH and provides an important mouse model for the exploration of matriptase function in ARIH, as well as multiple other physiological and pathological processes.

Asunto(s)

Enfermedades Genéticas Congénitas/enzimología , Hipotricosis/enzimología , Ictiosis/enzimología , Serina Endopeptidasas/metabolismo , Animales , Modelos Animales de Enfermedad , Epidermis/enzimología , Epidermis/patología , Proteínas Filagrina , Enfermedades Genéticas Congénitas/genética , Enfermedades Genéticas Congénitas/patología , Cabello/enzimología , Cabello/patología , Humanos , Hipotricosis/genética , Hipotricosis/patología , Ictiosis/genética , Ictiosis/patología , Proteínas de Filamentos Intermediarios/genética , Proteínas de Filamentos Intermediarios/metabolismo , Proteínas de la Membrana , Ratones , Ratones Mutantes , Mutación Missense , Estructura Terciaria de Proteína/genética , Serina Endopeptidasas/genética , Síndrome , Diente/enzimología , Diente/patología , Anomalías Dentarias/enzimología , Anomalías Dentarias/genética , Anomalías Dentarias/patología

RESUMEN

Recently, mutations in PNPLA2 encoding adipose triglyceride lipase (ATGL) were reported to underlie a neutral lipid storage disease (NLSD) subgroup characterized by mild myopathy and the absence of ichthyosis. In the present study a novel homozygous PNPLA2 mutation c.475_478dupCTCC (p.Gln160ProfsX19) in the patatin domain, the ATGL active site, was detected in a woman with NLSD and severe myopathy. The present results suggest that a premature truncation mutation in the patatin domain causes NLSD with severe myopathy.

Asunto(s)

Predisposición Genética a la Enfermedad/genética , Lipasa/genética , Trastornos del Metabolismo de los Lípidos/genética , Músculo Esquelético/enzimología , Enfermedades Musculares/genética , Mutación/genética , Adulto , Biopsia , Análisis Mutacional de ADN , Femenino , Marcadores Genéticos/genética , Humanos , Ictiosis/enzimología , Ictiosis/genética , Leucocitos/enzimología , Leucocitos/patología , Leucocitos/ultraestructura , Trastornos del Metabolismo de los Lípidos/enzimología , Errores Innatos del Metabolismo Lipídico/enzimología , Errores Innatos del Metabolismo Lipídico/genética , Errores Innatos del Metabolismo Lipídico/fisiopatología , Músculo Esquelético/patología , Músculo Esquelético/fisiopatología , Enfermedades Musculares/enzimología , Enfermedades Musculares/fisiopatología , Estructura Terciaria de Proteína/genética , Síndrome

RESUMEN

In this article, we describe a novel autosomal recessive ichthyosis with hypotrichosis syndrome, characterized by congenital ichthyosis associated with abnormal hair. Using homozygosity mapping, we mapped the disease locus to 11q24.3-q25. We screened the ST14 gene, which encodes matriptase, since transplantation of skin from matriptase(-/-)-knockout mice onto adult athymic nude mice has been shown elsewhere to result in an ichthyosislike phenotype associated with almost complete absence of erupted pelage hairs. Mutation analysis revealed a missense mutation, G827R, in the highly conserved peptidase S1-S6 domain. Marked skin hyperkeratosis due to impaired degradation of the stratum corneum corneodesmosomes was observed in the affected individuals, which suggests that matriptase plays a significant role in epidermal desquamation.

Asunto(s)

Genes Recesivos , Hipotricosis/genética , Ictiosis/genética , Proteínas de la Membrana/genética , Mutación/genética , Serina Endopeptidasas/genética , Adolescente , Secuencia de Aminoácidos , Niño , Preescolar , Cromosomas Humanos Par 11/genética , Femenino , Humanos , Hipotricosis/enzimología , Hipotricosis/patología , Ictiosis/enzimología , Ictiosis/patología , Masculino , Datos de Secuencia Molecular , Linaje , Homología de Secuencia de Aminoácido

RESUMEN

Bathing suit ichthyosis (BSI) is a striking and unique clinical form of autosomal recessive congenital ichthyosis characterized by pronounced scaling on the bathing suit areas but sparing of the extremities and the central face. Here we report on a series of 10 BSI patients. Our genetic, ultrastructural and biochemical investigations show that BSI is caused by transglutaminase-1 (TGase-1) deficiency. Altogether, we identified 13 mutations in TGM1-among them seven novel missense mutations and one novel nonsense mutation. Structural modeling for the Tyr276Asn mutation reveals that the residue is buried in the hydrophobic interior of the enzyme and that the hydroxyl side chain of Tyr276 is exposed to solvent in a cavity of the enzyme. Cryosections of healthy skin areas demonstrated an almost normal TGase activity, in contrast to the affected BSI skin, which only showed a cytoplasmic and clearly reduced TGase-1 activity. The distribution of TGase-1 substrates in the epidermis of affected skin corresponded to the situation in TGase-1 deficiency. Interestingly, the expression of TGase-3 and cathepsin D was reduced. Digital thermography validated a striking correlation between warmer body areas and presence of scaling in patients suggesting a decisive influence of the skin temperature. In situ TGase testing in skin of BSI patients demonstrated a marked decrease of enzyme activity when the temperature was increased from 25 to 37 degrees C. We conclude that BSI is caused by TGase-1 deficiency and suggest that it is a temperature-sensitive phenotype.

Asunto(s)

Ictiosis/genética , Transglutaminasas/deficiencia , Transglutaminasas/genética , Adolescente , Adulto , Niño , Preescolar , Mapeo Cromosómico , Codón sin Sentido , Femenino , Humanos , Ictiosis/enzimología , Ictiosis/patología , Lactante , Masculino , Modelos Moleculares , Mutación Missense , Fenotipo , Análisis de Secuencia de ADN , Piel/enzimología , Piel/patología , Temperatura , Transglutaminasas/química , Transglutaminasas/metabolismo

RESUMEN

BACKGROUND: Corneocytes of the nail plate, like those of the stratum corneum, generate cornified envelopes (CEs) of cross-linked protein that can be visualized readily after removal of non-cross-linked protein by detergent extraction. Defective CE formation occurs in epidermal scale and hair in transglutaminase 1 (TGM1)-negative lamellar ichthyosis (LI) and has been proposed as a diagnostic aid for this syndrome. OBJECTIVES: (i) To ascertain whether TGM1 is important for CE formation in nail; (ii) to characterize CE abnormalities occurring in LI that may be distinguished from other types of inherited ichthyosis when nail samples are subjected to detergent extraction; and (iii) to evaluate the utility of nails as a diagnostic aid for LI. METHODS: Nail samples were provided by nine patients previously classified as having TGM1-negative LI, four with other types of ichthyotic conditions and six normal controls. Samples were extracted extensively in sodium dodecyl sulphate under reducing conditions and examined by light and electron microscopy. RESULTS: After extraction, defective CE cross-linking was visualized in epidermal corneocytes from seven of nine patients exhibiting TGM1-negative LI, whereas nail samples from patients with the other syndromes were normal. The defects in CE structure resembled those recently reported for LI scale, although in some cases residual CE and CE-associated structures were present. CONCLUSIONS: Despite the paucity of clinical nail symptoms in LI, TGM1 activity is important for generation of normal CE in nail plate, consistent with its importance in protein cross-linking in interfollicular epidermis and hair. Lack of this activity leads to a strikingly aberrant appearance of CE in LI nail after detergent extraction that is evident ultrastructurally in a large majority of cases. Nail envelopes therefore could provide a useful diagnostic tool in distinguishing LI from other ichthyoses with overlapping clinical features.

Asunto(s)

Ictiosis Lamelar/patología , Enfermedades de la Uña/patología , Diagnóstico Diferencial , Epidermis/enzimología , Epidermis/ultraestructura , Humanos , Ictiosis/enzimología , Ictiosis/patología , Ictiosis Lamelar/enzimología , Enfermedades de la Uña/enzimología , Uñas/química , Dodecil Sulfato de Sodio , Manejo de Especímenes/métodos , Transglutaminasas/deficiencia , Transglutaminasas/fisiología

RESUMEN

Profilaggrin is a large epidermal polyprotein that is proteolytically processed during keratinocyte differentiation to release multiple filaggrin monomer units as well as a calcium-binding regulatory NH2-terminal filaggrin S-100 protein. We show that epidermal deficiency of the transmembrane serine protease Matriptase/MT-SP1 perturbs lipid matrix formation, cornified envelope morphogenesis, and stratum corneum desquamation. Surprisingly, proteomic analysis of Matriptase/MT-SP1-deficient epidermis revealed the selective loss of both proteolytically processed filaggrin monomer units and the NH2-terminal filaggrin S-100 regulatory protein. This was associated with a profound accumulation of profilaggrin and aberrant profilaggrin-processing products in the stratum corneum. The data identify keratinocyte Matriptase/MT-SP1 as an essential component of the profilaggrin-processing pathway and a key regulator of terminal epidermal differentiation.

Asunto(s)

Epidermis/enzimología , Epidermis/crecimiento & desarrollo , Proteínas de Filamentos Intermediarios/biosíntesis , Queratinocitos/enzimología , Serina Endopeptidasas/deficiencia , Tripsina/deficiencia , Animales , Diferenciación Celular/genética , Deshidratación/enzimología , Epidermis/patología , Matriz Extracelular/genética , Matriz Extracelular/metabolismo , Matriz Extracelular/patología , Proteínas Filagrina , Ictiosis/enzimología , Ictiosis/genética , Ictiosis/patología , Proteínas de Filamentos Intermediarios/deficiencia , Proteínas de Filamentos Intermediarios/metabolismo , Queratinocitos/patología , Queratinocitos/ultraestructura , Metabolismo de los Lípidos , Proteínas de la Membrana , Ratones , Ratones Noqueados , Microscopía Electrónica , Péptido Hidrolasas/deficiencia , Péptido Hidrolasas/genética , Permeabilidad , Precursores de Proteínas/metabolismo , Proteínas S100/metabolismo , Serina Endopeptidasas/genética , Anomalías Cutáneas/enzimología , Anomalías Cutáneas/genética , Anomalías Cutáneas/patología , Tripsina/genética

RESUMEN

OBJECTIVE: Stratum corneum chymotryptic enzyme (SCCE) is a serine protease, which is thought to play a role in the desquamation of skin via the proteolysis of desmosomes in the stratum corneum. The objective of this study was to investigate the expression of SCCE in ichthyoses and squamoproliferative processes, conditions in which the shedding and replacement of epidermal cells is disrupted. DESIGN: Tissue samples from cases of Netherton's syndrome, congenital ichthyosiform erythroderma, ichthyosis vulgaris, actinic keratosis, squamous cell carcinoma in situ, and invasive squamous cell carcinoma were examined for expression of SCCE using immunohistochemistry. MAIN OUTCOME MEASURES: The slides were qualitatively analyzed for the expression of SCCE by a certified dermatopathologist. RESULTS: In all disease states, we found that the expression of SCCE was absent in areas of parakeratotic stratum corneum of normal thickness. In areas of mixed orthokeratosis and parakeratosis where the stratum corneum was greatly thickened as might correspond clinically to a cutaneous horn, SCCE staining was either absent or focally aggregated without regard to orthokeratosis or parakeratosis. Of note, complete absence of SCCE expression was not observed in any of the cases of ichthyosis examined, nor was there increased expression of SCCE in the atypical cells of the squamoproliferative disorders. CONCLUSIONS: These results suggest that SCCE is abnormally expressed in skin where epidermal cell kinetics are disrupted due to inherited and acquired defects. Further investigation is needed to determine causality between the abnormal expression of SCCE and the altered cell kinetics in these diseases.

Asunto(s)

Carcinoma in Situ/enzimología , Ictiosis/enzimología , Neoplasias de Células Escamosas/enzimología , Trastornos por Fotosensibilidad/enzimología , Serina Endopeptidasas/metabolismo , Neoplasias Cutáneas/enzimología , Carcinoma in Situ/patología , Epidermis/enzimología , Epidermis/patología , Técnica del Anticuerpo Fluorescente Indirecta , Humanos , Calicreínas , Neoplasias de Células Escamosas/patología , Trastornos por Fotosensibilidad/patología , Neoplasias Cutáneas/patología , Luz Solar/efectos adversos

RESUMEN

Transglutaminase 1 (TGase 1) is one of the genes implicated in autosomal recessive congenital ichthyosis. Skin from TGase 1(-/-) mice, which die as neonates, lacks the normal insoluble cornified envelope and has impaired barrier function. Characterization of in situ dye permeability and transepidermal water loss revealed defects in the development of the skin permeability barrier in TGase 1(-/-) mice. In the stratum corneum of the skin, tongue, and forestomach, intercellular lipid lamellae were disorganized, and the corneocyte lipid envelope and cornified envelope were lacking. Neonatal TGase 1(-/-) mouse skin was taut and erythrodermic, but transplanted TGase 1(-/-) mouse skin resembled that seen in severe ichthyosis, with epidermal hyperplasia and marked hyperkeratosis. Abnormalities in those barrier structures remained, but transepidermal water loss was improved to control levels in the ichthyosiform skin. From these results, we conclude that TGase 1 is essential to the assembly and organization of the barrier structures in stratified squamous epithelia. We suggest that the ichthyosiform skin phenotype in TGase 1 deficiency develops the massive hyperkeratosis as a physical compensation for the defective cutaneous permeability barrier required for survival in a terrestrial environment.

Asunto(s)

Ictiosis/enzimología , Piel/fisiopatología , Transglutaminasas/fisiología , Animales , Femenino , Ictiosis/patología , Ictiosis/fisiopatología , Lípidos , Masculino , Ratones , Ratones Endogámicos C57BL , Ratones Noqueados , Ratones Desnudos , Permeabilidad , Fenotipo , Piel/embriología , Piel/patología , Transglutaminasas/genética