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LL-37

Cathelicidin, hCAP-18, FALL-39, CAP-18

Quick Stats
Studies 2230
Trials 95
Score 2
2005 pubmed 73 citations

Expression and modulation of LL-37 in normal human keratinocytes, HaCaT cells, and inflammatory skin diseases.

Kim. Ji Eun JE; Kim. Beom Joon BJ; Jeong. Mi Sook MS; Seo. Seong Jun SJ; Kim. Myeung Nam MN; Hong. Chang Kwun CK; Ro. Byung In BI

Key Findings

  • Normal human keratinocytes produce LL‑37, while HaCaT cells do not
  • UV‑B irradiation and lipopolysaccharide (LPS) increase LL‑37 expression in normal cells
  • Psoriatic skin contains high levels of LL‑37 compared to atopic dermatitis or healthy skin

Practical Outcomes

  • UV‑B exposure can boost the skin’s antimicrobial defenses, but the benefit is modest and must be balanced against skin‑damage risks. There’s no clear protocol for using LL‑37 directly, but the findings suggest that controlled sun exposure or topical agents that mimic bacterial signals might modestly enhance skin immunity.

Summary

The study shows that the skin’s natural antimicrobial peptide LL‑37 is made by normal skin cells but not by a common lab‑grown skin cell line, and its production goes up after UV‑B light or bacterial components, especially in psoriasis‑affected skin.

Abstract

Defensins and cathelicidins (LL-37) are major antimicrobial peptides (AMPs) of the innate immune system of the human skin. In normal non-inflamed skin these peptides are negligible, but their expression can be markedly increased in inflammatory skin disease such as psoriasis. We designed this study to identify the expressions of LL-37 in normal human keratinocyte (NHK) and HaCaT cells after exposure to stimulants and to investigate difference of LL-37 expression accompanied with cell differentiation status, and come to understand difference of susceptibility to infection in atopic dermatitis and psoriasis. Expressions of LL-37 in NHKs and HaCaT cells were evaluated by using RT-PCR, Western blotting, and immunohistochemical (IHC) staining at 6, 12, and 24 hr post stimulation after exposure to Ultraviolet B irradiation and lipopolysaccharide. And expression of LL-37 in skin biopsy specimens from patients with atopic dermatitis and psoriasis was determined by immunohistochemical analysis. In time-sequential analyses of LL-37 expression revealed that LL-37 was expressed in NHKs, but not in HaCaT cells. IHC analysis confirmed the presence of abundant LL-37 in the epidermis of psoriasis. Therefore we deduced that expression of LL-37 is affected by UV irradiation, bacterial infection, and status of cell differentiation.

Study Information

Provider

pubmed

Year

2005

Date

2005-08-01T00:00:00.000Z

DOI

10.3346/jkms.2005.20.4.649

Citations

73

References

30