Dynamic expression of epidermal caspase 8 simulates a wound healing response

Top Cited Papers
Open Access
Publisher Website
Google Scholar
Abstract
This paper provides evidence for a role of caspase 8 in skin homeostasis. Loss of epidermal caspase 8, an important mediator of apoptosis, promotes several phases of the wound healing response in mice, including epidermal cell proliferation and inflammation. The findings illustrate how the loss of caspase 8 can have an impact beyond programmed cell death to affect the local microenvironment and elicit processes common to wound repair and many neoplastic skin disorders. This paper provides evidence for a role of caspase 8 in skin homeostasis. Loss of epidermal caspase 8 promotes epidermal cell proliferation and inflammation, and authors propose that caspase 8 expression by keratinocytes in the granular layer limits the release of preformed IL1α. Tissue homeostasis and regeneration are regulated by an intricate balance of seemingly competing processes—proliferation versus differentiation, and cell death versus survival1. Here we demonstrate that the loss of epidermal caspase 8, an important mediator of apoptosis2, recapitulates several phases of a wound healing response in the mouse. The epidermal hyperplasia in the caspase 8 null skin is the culmination of signals exchanged between epidermal keratinocytes, dermal fibroblasts and leukocytic cells. This reciprocal interaction is initiated by the paracrine signalling of interleukin 1α (IL1α), which activates both skin stem cell proliferation and cutaneous inflammation. The non-canonical secretion of IL1α is induced by a p38-MAPK-mediated upregulation of NALP3 (also known as NLRP3), leading to inflammasome assembly and caspase 1 activation. Notably, the increased proliferation of basal keratinocytes is counterbalanced by the growth arrest of suprabasal keratinocytes in the stratified epidermis by IL1α-dependent NFκB signalling. Altogether, our findings illustrate how the loss of caspase 8 can affect more than programmed cell death to alter the local microenvironment and elicit processes common to wound repair and many neoplastic skin disorders.