期刊
EXPERIMENTAL DERMATOLOGY
卷 -, 期 -, 页码 -出版社
WILEY
DOI: 10.1111/exd.14772
关键词
Filaggrin; KLICK syndrome; proteasome; proteolysis
类别
The absence of a functional proteasome in the suprabasal layers of the epidermis causes keratosis linearis with ichthyosis congenita and sclerosing keratoderma syndrome. Inhibited proteasome proteolytic activity leads to down-regulation of filaggrin expression and perturbation of urocanic acid and pyrrolidone carboxylic acid production. Accumulation of small cytoplasmic vesicles and activation of autophagy markers were observed upon proteasome inhibition.
Absence of a functional proteasome in the suprabasal layers of the epidermis is responsible for keratosis linearis with ichthyosis congenital and sclerosing keratoderma syndrome. Patient epidermis shows hypergranulosis associated with abnormally shaped keratohyalin granules and abnormal distribution of filaggrin in the Stratum granulosum and Stratum corneum. This suggests that the proteasome is involved in the degradation of filaggrin. To test this hypothesis, the proteasome proteolytic activity was inhibited in 3D reconstructed human epidermis (RHE) with the specific clasto-lactacystin beta-lactone inhibitor. Confirming the efficacy of inhibition, ubiquitinated proteins accumulated in treated RHEs as compared to controls. Levels of urocanic acid (UCA) and pyrrolidone carboxylic acid (PCA), the end products of filaggrin degradation, were reduced. However, neither filaggrin accumulation nor appearance of filaggrin-derived peptides were observed. On the contrary, the amount of filaggrin was shown to decrease, and a similar tendency was observed for profilaggrin, its precursor. Accumulation of small cytoplasmic vesicles associated with a significant increase in autophagy markers indicated activation of the autophagy process upon proteasome inhibition. Taken together, these results suggest that the perturbation of UCA and PCA production after proteasome inhibition was probably due to down-regulation of filaggrin expression rather than to blocking of filaggrin proteolysis.
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