1. Academic Validation
  2. TLN-58, an Additional hCAP18 Processing Form, Found in the Lesion Vesicle of Palmoplantar Pustulosis in the Skin

TLN-58, an Additional hCAP18 Processing Form, Found in the Lesion Vesicle of Palmoplantar Pustulosis in the Skin

  • J Invest Dermatol. 2017 Feb;137(2):322-331. doi: 10.1016/j.jid.2016.07.044.
Masamoto Murakami 1 Kenji Kameda 2 Hiroki Tsumoto 3 Teruko Tsuda 4 Kana Masuda 4 Ryo Utsunomiya 4 Hideki Mori 4 Yuri Miura 3 Koji Sayama 4
Affiliations

Affiliations

  • 1 Department of Dermatology, Ehime University Graduate School of Medicine, Ehime, Japan. Electronic address: mamuraka@m.ehime-u.ac.jp.
  • 2 Advanced Research Support Center, Ehime University Graduate School of Medicine, Ehime, Japan.
  • 3 Tokyo Metropolitan Institute of Gerontology, Tokyo, Japan.
  • 4 Department of Dermatology, Ehime University Graduate School of Medicine, Ehime, Japan.
Abstract

We previously reported that the early vesicle of the palmoplantar pustulosis (PPP) vesicle originated from eccrine sweat in the acrosyringium and that the PPP vesicle contains the antimicrobial peptide human cathelicidin-18/LL-37. The concentration of LL-37 was sufficient to induce the subsequent inflammation in lesions and human keratinocytes, and the PPP vesicles contained additional small fragments of human cathelicidin-18, of approximately 7 kDa, which have not been identified. The aim of the present study was to clarify the additional processed forms found in PPP vesicles and their physiological effects on normal keratinocytes and sweat gland cells. Lesional PPP vesicles were collected from PPP patients, and endogenous human cathelicidin-18/LL-37 was depleted using a LL-37 antibody affinity column. A designed recombinant human cathelicidin-18 peptide was prepared and incubated with the depleted PPP vesicle fluid to confirm the additional processed form. In-gel digestion analysis and protein Sequencing confirmed the additional form as TLN-58. TLN-58 up-regulated IL-17C, IL-8, IL-23, IL-1α, and IL-1β mRNA and protein expression in normal human keratinocytes and also showed Antibacterial activity against Staphylococcus aureus, Staphylococcus epidermidis, and group A Streptococcus species, similar to LL-37. This additional form could be involved in the continued inflammation in PPP lesions.

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