The trypsin-like serine protease marapsin is a member of the large protease gene cluster at human chromosome 16p13.3, which also contains the structurally related proteases testisin, tryptase ⑀, tryptase ␥, and EOS. To gain insight into the biological functions of marapsin, we undertook a detailed gene expression analysis. It showed that marapsin expression was restricted to tissues containing stratified squamous epithelia and was absent or only weakly expressed in all other tissues, including the pancreas. Marapsin was constitutively expressed in nonkeratinizing stratified squamous epithelia of human esophagus, tonsil, cervix, larynx, and cornea. In the keratinizing stratified squamous epidermis of skin, however, its expression was induced only during epidermal hyperproliferation, such as in psoriasis and in murine wound healing. In fact, marapsin was the second most strongly up-regulated protease in psoriatic lesions, where expression was localized to the upper region of the hyperplastic epidermis. Similarly, in the hyperproliferative epithelium of regenerating murine skin wounds, marapsin localized to the suprabasal layers, where keratinocytes undergo squamous differentiation. The transient up-regulation of marapsin, which closely correlated with re-epithelialization, was virtually absent in a genetic mouse model of delayed wound closure. These results suggested a function during the process of re-epithelialization. Furthermore, in reconstituted human epidermis, a model system of epidermal differentiation, members of the IL-20 subfamily of cytokines, such as IL-22, induced marapsin expression. Consistent with a physiologic role in marapsin regulation, IL-22 was also strongly expressed in re-epithelializing skin wounds. Marapsin's restricted expression, localization, and cytokine-inducible expression suggest a role in the terminal differentiation of keratinocytes in hyperproliferating squamous epithelia.Marapsin (PRSS27; also known as pancreasin) is a trypsinlike serine protease and member of the large serine protease gene cluster at human chromosome 16p13.3 and mouse chromosome 17A3.3, respectively (1, 2). Based on conserved features of the propeptides and the activation mechanism, these proteases were divided into two groups (2). Marapsin belongs to the group-1 subfamily of the human cluster, which includes testisin (PRSS21, eosinophil serine protease-1), tryptase ⑀ (PRSS22, brain-specific serine protease-4), tryptase ␥ (PRSS31, transmembrane tryptase), and EOS (PRSS33). They all contain a relatively short propeptide, which, after activation cleavage of the single chain precursor, remains attached to the protease domain via a disulfide bond. In contrast, the propeptides of group-2 subfamily members tryptase ␣, tryptase 1, tryptase 2, and tryptase ␦ are not disulfide-linked to the protease domain and are released upon activation cleavage.The 268-amino acid single-chain precursor form (zymogen) of human marapsin is converted into the active enzyme by proteolytic cleavage at the Arg 34 -Met 35 peptide bond. T...