HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Cathepsin K is involved in development of psoriasis-like skin lesions through TLR-dependent Th17 activation.

Abstract
Cathepsins (CTSs) are lysosomal cysteine proteases that play an important role in the turnover of intracellular proteins and extracellular proteins, such as the degradation of extracellular matrices and the processing of antigenic proteins. A CTS inhibitor, NC-2300, not only suppresses bone erosion by inhibition of cathepsin K (CTSK), but also ameliorates paw swelling at inflamed joints in adjuvant-induced arthritis in rats. It has been demonstrated that the amelioration of joint inflammation by NC-2300 is mediated by the downregulation of cytokine expression in dendritic cells, which are essential for Th17 activation. In this work, we studied the role for CTSs in the pathogenesis of psoriasis-like lesion in K5.Stat3C mice, a mouse model of psoriasis, in which Th17 contributes to lesion development similar to psoriasis. Psoriatic lesions expressed increased levels of Ctsk and Ctss mRNA compared with uninvolved skin and normal control skin. Similarly, the epidermis and dermis in K5.Stat3C mice demonstrated increased CTSK activities, which were sensitive to NC-2300. Topical treatment with NC-2300 significantly ameliorated 12-O-tetradecanoylphorbol-13-acetate-induced psoriasis-like lesions in K5.Stat3C mice, and downregulated the expression of IL-12, IL-23, and Th17 cytokines. In vitro experiments revealed that TLR7 activation of bone marrow-derived myeloid dendritic cells led to increase in IL-23 at mRNA and protein levels, which were downregulated by NC-2300. These results suggest that CTSK plays a role in development of psoriatic lesions through TLR7-dependent Th17 polarization.
AuthorsToshitake Hirai, Takashi Kanda, Kenji Sato, Mikiro Takaishi, Kimiko Nakajima, Mayuko Yamamoto, Reiko Kamijima, John Digiovanni, Shigetoshi Sano
JournalJournal of immunology (Baltimore, Md. : 1950) (J Immunol) Vol. 190 Issue 9 Pg. 4805-11 (May 01 2013) ISSN: 1550-6606 [Electronic] United States
PMID23543761 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Interleukin-23
  • RNA, Messenger
  • Toll-Like Receptor 7
  • Toll-Like Receptor 8
  • Interleukin-12
  • Cathepsin K
Topics
  • Animals
  • Bone Marrow (immunology, metabolism, pathology)
  • Cathepsin K (genetics, immunology, metabolism)
  • Dermis (enzymology, immunology, pathology)
  • Down-Regulation
  • Epidermis (enzymology, immunology, pathology)
  • Female
  • Humans
  • Interleukin-12 (genetics, immunology, metabolism)
  • Interleukin-23 (genetics, immunology, metabolism)
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Myeloid Cells (immunology, metabolism, pathology)
  • Psoriasis (enzymology, genetics, immunology, pathology)
  • RNA, Messenger (genetics, metabolism)
  • Th17 Cells (enzymology, immunology, pathology)
  • Toll-Like Receptor 7 (genetics, immunology, metabolism)
  • Toll-Like Receptor 8 (genetics, immunology, metabolism)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: