Collagen VII half-life at the dermal-epidermal junction zone: implications for mechanisms and therapy of genodermatoses

The tissue half-life of proteins largely determines treatment frequency of non-gene-editing-based therapies targeting the cause of genodermatoses. Surprisingly, such knowledge is missing for a vast number of proteins involved in pathologies. The dermal-epidermal junction zone is believed to be a rat...

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Bibliographic Details
Main Authors: Kühl, Tobias Hans-Jürgen (Author) , Haußer-Siller, Ingrid (Author)
Format: Article (Journal)
Language:English
Published: 29 March 2016
In: The journal of investigative dermatology
Year: 2016, Volume: 136, Issue: 6, Pages: 1116-1123
ISSN:1523-1747
DOI:10.1016/j.jid.2016.02.002
Online Access:Verlag, Volltext: https://doi.org/10.1016/j.jid.2016.02.002
Verlag, Volltext: http://www.sciencedirect.com/science/article/pii/S0022202X16004838
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Author Notes:Tobias Kühl, Markus Mezger, Ingrid Hausser, Lin T. Guey, Rupert Handgretinger, Leena Bruckner-Tuderman and Alexander Nyström
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Summary:The tissue half-life of proteins largely determines treatment frequency of non-gene-editing-based therapies targeting the cause of genodermatoses. Surprisingly, such knowledge is missing for a vast number of proteins involved in pathologies. The dermal-epidermal junction zone is believed to be a rather static structure, but to our knowledge no detailed analysis of the stability of proteins within this zone has been performed. Here, we addressed the in vivo half-life of collagen type VII using genetic ablation of its expression and therapeutic introduction of exogenous collagen VII in a preclinical model. A similar in vivo stability of collagen VII was observed in the skin, tongue, and esophagus, with a half-life of about 1 month. Collagen VII expressed by intradermally injected mesenchymal stromal cells also exhibited a similar half-life. Our study provides key information needed for the development of protein replacement or cell-based therapies for dystrophic epidermolysis bullosa caused by genetic deficiency of collagen VII. Moreover, by showing what we define as an intermediate half-life of collagen VII, our study challenges the view of the dermal-epidermal junction zone as a static structure with very slow turnover.
Item Description:Gesehen am 04.09.2019
Physical Description:Online Resource
ISSN:1523-1747
DOI:10.1016/j.jid.2016.02.002