Abstract
While the study of full‐thickness human skin organ culture (hSOC) has many advantages over so‐called 3D skin "equivalents" in terms of physiological relevance, one major limitation of both systems is that they are routinely performed under conditions of disrupted perfusion and denervation (for discussion, see 1). This limitation needs to be kept in mind whenever skin properties are investigated that depend on or are closely associated with functional sensory skin nerves, such as neurogenic skin inflammation and the role of (often innervated!) mast cell (s1) in it.
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