Literature DB >> 25565224

Cellular basis of secondary infections and impaired desquamation in certain inherited ichthyoses.

Aegean Chan1, Elena Godoy-Gijon1, Almudena Nuno-Gonzalez1, Debra Crumrine1, Melanie Hupe1, Eung-Ho Choi2, Robert Gruber3, Mary L Williams4, Keith Choate5, Philip H Fleckman6, Peter M Elias1.   

Abstract

IMPORTANCE: Secondary infections and impaired desquamation complicate certain inherited ichthyoses, but their cellular basis remains unknown. In healthy human epidermis, the antimicrobial peptides cathelicidin (LL-37) and human β-defensin 2 (HBD2), as well as the desquamatory protease kallikrein-related peptidase 7 (KLK7), are delivered to the stratum corneum (SC) interstices by lamellar body (LB) exocytosis.
OBJECTIVE: To assess whether abnormalities in the LB secretory system could account for increased risk of infections and impaired desquamation in inherited ichthyoses with known abnormalities in LB assembly (Harlequin ichthyosis [HI]), secretion (epidermolytic ichthyosis [EI]), or postsecretory proteolysis (Netherton syndrome [NS]). DESIGN, SETTING, AND PARTICIPANTS: Samples from library material were taken from patients with HI, EI, NS, and other ichthyoses, but with a normal LB secretory system, and in healthy controls and were evaluated by electron microscopy and immunohistochemical analysis from July 1, 2010, through March 31, 2013. MAIN OUTCOME AND MEASURES: Changes in LB secretion and in the fate of LB-derived enzymes and antimicrobial peptides in ichthyotic patients vs healthy controls.
RESULTS: In healthy controls and patients with X-linked ichthyosis, neutral lipid storage disease with ichthyosis, and Gaucher disease, LB secretion is normal, and delivery of LB-derived proteins and LL-37 immunostaining persists high into the SC. In contrast, proteins loaded into nascent LBs and their delivery to the SC interstices decrease markedly in patients with HI, paralleled by reduced immunostaining for LL-37, HBD2, and KLK7 in the SC. In patients with EI, the cytoskeletal abnormality impairs the exocytosis of LB contents and thus results in decreased LL-37, HBD2, and KLK7 secretion, causing substantial entombment of these proteins within the corneocyte cytosol. Finally, in patients with NS, although abundant enzyme proteins loaded in parallel with accelerated LB production, LL-37 disappears, whereas KLK7 levels increase markedly in the SC. CONCLUSIONS AND RELEVANCE: Together, these results suggest that diverse abnormalities in the LB secretory system account for the increased risk of secondary infections and impaired desquamation in patients with HI, EI, and NS.

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Year:  2015        PMID: 25565224      PMCID: PMC4498571          DOI: 10.1001/jamadermatol.2014.3369

Source DB:  PubMed          Journal:  JAMA Dermatol        ISSN: 2168-6068            Impact factor:   10.282


  33 in total

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Journal:  Adv Dermatol       Date:  2007

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Authors:  Kaori Sakai; Masashi Akiyama; Yoriko Sugiyama-Nakagiri; James R McMillan; Daisuke Sawamura; Hiroshi Shimizu
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3.  Harlequin ichthyosis: a review of clinical and molecular findings in 45 cases.

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Review 4.  Congenital ichthyosis: an overview of current and emerging therapies.

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5.  Co-regulation and interdependence of the mammalian epidermal permeability and antimicrobial barriers.

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10.  Urea uptake enhances barrier function and antimicrobial defense in humans by regulating epidermal gene expression.

Authors:  Susanne Grether-Beck; Ingo Felsner; Heidi Brenden; Zippora Kohne; Marc Majora; Alessandra Marini; Thomas Jaenicke; Marina Rodriguez-Martin; Carles Trullas; Melanie Hupe; Peter M Elias; Jean Krutmann
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2.  A case report of fatal harlequin ichthyosis: Insights into infectious and respiratory complications.

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3.  Defects in Stratum Corneum Desquamation Are the Predominant Effect of Impaired ABCA12 Function in a Novel Mouse Model of Harlequin Ichthyosis.

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Review 4.  Inherited Nonsyndromic Ichthyoses: An Update on Pathophysiology, Diagnosis and Treatment.

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Review 8.  Ichthyosis: A Road Model for Skin Research.

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9.  Activation of Molecular Signatures for Antimicrobial and Innate Defense Responses in Skin with Transglutaminase 1 Deficiency.

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