Literature DB >> 29143961

Upregulation of epidermal gap junctional proteins in patients with venous disease.

M Kanapathy1,2,3, R Simpson1, L Madden3, C Thrasivoulou4, A Mosahebi1,2, D L Becker3,5, T Richards1.   

Abstract

BACKGROUND: Leg ulceration is a feared complication of venous insufficiency. It is not known whether varicose veins predispose skin to poor wound healing. The expression pattern of gap junctional protein connexin, a known marker of poor wound healing, was investigated across various stages of venous disease.
METHODS: Patients undergoing intervention for varicose veins were assessed according to the Clinical Etiologic Anatomic Pathophysiologic (CEAP) classification of varicose veins. Paired 4-mm punch biopsies were taken from above the ankle (pathological) and above the knee (control). Tissues were stained with haematoxylin and eosin, and for connexin 43, connexin 30 and connexin 26.
RESULTS: Forty-eight paired biopsies were taken (12 each for CEAP class C0, C2, C4 and C6). The pathological skin showed progressive epithelial hyperthickening, an increase in the number and depth of rete ridges, increased inflammation and loss of dermal architecture with disease progression from C4 onwards. The overall absolute connexin expression and mean connexin expression per cell in the pathological skin similarly increased across the CEAP classes from as early as C2. Increasing levels of connexin in control skin were also noted, indicating progression of the disease proximally. Connexin 43 expression showed the strongest positive correlation between pathological and control skin.
CONCLUSION: Connexins were overexpressed in patients with simple varicose veins, with a stepwise increased expression through venous eczema to ulceration. Connexin 43 is a potential biomarker for venous disease. This finding suggests that varicose veins predispose skin to poor wound healing. Surgical relevance The overexpression of connexins, a family of gap junctional proteins, is known to cause poor healing in venous leg ulceration. It is not known whether there is any association with superficial venous disease. Here, connexin proteins were overexpressed in patients with uncomplicated varicose veins, before histological skin changes. Connexin could be a biomarker of venous disease progression.
© 2017 BJS Society Ltd Published by John Wiley & Sons Ltd.

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Year:  2017        PMID: 29143961     DOI: 10.1002/bjs.10653

Source DB:  PubMed          Journal:  Br J Surg        ISSN: 0007-1323            Impact factor:   6.939


  4 in total

Review 1.  Connexin 43-Based Therapeutics for Dermal Wound Healing.

Authors:  Jade Montgomery; Gautam S Ghatnekar; Christina L Grek; Kurtis E Moyer; Robert G Gourdie
Journal:  Int J Mol Sci       Date:  2018-06-15       Impact factor: 5.923

Review 2.  Connexins and the Epithelial Tissue Barrier: A Focus on Connexin 26.

Authors:  Laura Garcia-Vega; Erin M O'Shaughnessy; Ahmad Albuloushi; Patricia E Martin
Journal:  Biology (Basel)       Date:  2021-01-14

3.  Extracellular matrix and cellular senescence in venous leg ulcers.

Authors:  Debbie X E Lim; Toby Richards; Muholan Kanapathy; Thankiah Sudhaharan; Graham D Wright; Anthony R J Phillips; David L Becker
Journal:  Sci Rep       Date:  2021-10-11       Impact factor: 4.379

4.  The connexin 43 carboxyl terminal mimetic peptide αCT1 prompts differentiation of a collagen scar matrix in humans resembling unwounded skin.

Authors:  Jade Montgomery; William J Richardson; Spencer Marsh; J Matthew Rhett; Francis Bustos; Katherine Degen; Gautam S Ghatnekar; Christina L Grek; L Jane Jourdan; Jeffrey W Holmes; Robert G Gourdie
Journal:  FASEB J       Date:  2021-08       Impact factor: 5.834

  4 in total

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