Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Postsecretory processing generates multiple cathelicidins for enhanced topical antimicrobial defense.

Masamoto Murakami1, Belen Lopez-Garcia, Marissa Braff

  • 1Division of Dermatology, University of California, and Veterans Affairs San Diego Healthcare Center, San Diego, CA 92161, USA.

Journal of Immunology (Baltimore, Md. : 1950)
|February 24, 2004
PubMed
Summary

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Fibroblast-derived CCL2 orchestrates immune responses and defends against Staphylococcus aureus skin infection.

Cellular & molecular immunology·2026
Same author

Treatment Guidance for Palmoplantar Pustulosis 2022.

The Journal of dermatology·2026
Same author

Disease context dictates the cellular targets of IL-17 in inflammatory skin disease.

bioRxiv : the preprint server for biology·2026
Same author

Part I. The role of Staphylococcus aureus in the pathophysiology of dermatologic disease.

Journal of the American Academy of Dermatology·2026
Same author

Dermal fibroblasts respond to IL-4 and IL-13 and promote T cell recruitment in atopic dermatitis.

The Journal of clinical investigation·2026
Same author

Staphylococcus aureus in atopic dermatitis: How a common bacterium exploits and drives disease.

The Journal of allergy and clinical immunology·2026

Human skin produces novel antimicrobial peptides from the CAMP gene product, distinct from LL-37. These new peptides enhance direct killing of skin pathogens like Staphylococcus aureus and Candida albicans.

Area of Science:

  • Microbiology
  • Immunology
  • Dermatology

Background:

  • Antimicrobial peptides are crucial for host defense against infections.
  • Human skin utilizes genes like DCD and CAMP for antimicrobial peptide production, including dermcidin and LL-37.
  • Many antimicrobial peptides possess dual functions, acting as antibiotics and modulating host immune responses.

Purpose of the Study:

  • To investigate the processing of the CAMP gene product on the skin surface.
  • To characterize novel antimicrobial peptides derived from CAMP.
  • To evaluate the antimicrobial and immunomodulatory activities of these novel peptides.

Main Methods:

  • Analysis of CAMP gene product processing via serine protease-dependent mechanisms.
  • Characterization of newly generated antimicrobial peptides.

Related Experiment Videos

  • Assessment of antimicrobial activity against skin pathogens (Staphylococcus aureus, Candida albicans).
  • Evaluation of IL-8 release from keratinocytes to determine inflammatory response modulation.
  • Main Results:

    • The CAMP gene product is processed into multiple novel antimicrobial peptides on the skin surface, distinct from LL-37.
    • These novel peptides exhibit enhanced antimicrobial activity, effectively killing Staphylococcus aureus and Candida albicans.
    • The inflammatory stimulatory activity (IL-8 release) associated with LL-37 is lost in the processed peptides.
    • The functional shift favors direct microbial inhibition over immune modulation in the topical environment.

    Conclusions:

    • The CAMP gene product undergoes unique processing in the skin's topical environment.
    • This processing generates novel antimicrobial peptides with potent direct antimicrobial action.
    • The functional adaptation of these peptides enhances pathogen clearance and reduces potential inflammation, optimizing skin defense.