AI Article Synopsis

  • Hidradenitis suppurativa/acne inversa (HS) is a chronic skin disease that affects hair follicles, leading to significant inflammation and tissue changes.
  • An ex vivo culture model using skin biopsies from HS patients revealed altered collagen organization and increased fragmentation of elastin fibers, indicating matrix remodelling.
  • Elevated levels of MMP-2 and MMP-9 were found in HS skin, suggesting that these enzymes may play a role in inflammation by affecting the extracellular matrix and could provide insights into HS's inflammatory mechanisms.

Article Abstract

Hidradenitis suppurativa/acne inversa (HS) is a chronic, inflammatory, recurrent, debilitating skin disease of the hair follicle, associated with considerable tissue remodelling. Although abnormal cytokine expression was detected both in perilesional and in uninvolved skin, up to now there is no model allowing a better understanding of the implicit inflammatory mechanisms in HS. The aim of this study was to investigate the inflammatory response in HS skin by mean of an ex vivo model culture. To that purpose, nine skin biopsy specimens from patients suffering from HS and controls were cultured up to 4 days. Microscopy imaging investigations showed variations of collagen I and III organization, and an increase in elastin fibres fragmentation in HS skin after 4 days of culture. The HS matrix structure remodelling was associated with high level of MMP-2 and MMP-9 in HS lesional skin. After 4 days of culture, the MMP expression in HS perilesional skin reached the level observed in HS lesional skin. Concomitantly, an increase in IL-1β concentration was observed in all skin samples after 4 days of culture, although IL-1β concentrations remained significantly higher in HS lesional skin as compared with control skin. Meanwhile, neither IL-17 concentrations nor the inflammasome components NLRP3 and caspase-1 varied. Thus, our HS skin model culture showed that MMP-induced matrix alteration could participate in HS inflammation by releasing biological active peptides and inflammatory factors from the extracellular matrix (ECM), and open new opportunities to investigate the regulation of the inflammatory mechanism associated with HS.

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Source
http://dx.doi.org/10.1111/exd.13919DOI Listing

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