Differential regulation of human cathelicidin LL-37 by free fatty acids and their analogs

Peptides. 2013 Dec:50:129-38. doi: 10.1016/j.peptides.2013.10.008. Epub 2013 Oct 18.

Abstract

LL-37 is the single cathelicidin host defense peptide in humans with direct antimicrobial and immunomodulatory activities. Specific regulation of LL-37 synthesis has emerged as a novel non-antibiotic approach to disease control and prevention. Short-chain fatty acids, and butyrate in particular, were found recently to be strong inducers of LL-37 gene expression without causing inflammation. Here, we further evaluated the LL-37-inducing efficiency of a broad range of saturated free fatty acids and their derivatives in human HT-29 colonic epithelial cells and U-937 monocytic cells by real-time RT-PCR. Surprisingly, we revealed that valerate, hexanoate, and heptanoate with 5-7 carbons are more potent than 4-carbon butyrate in promoting LL-37 gene expression in both cell types. Free fatty acids with longer than 7 or shorter than 4 carbons showed only a marginal effect on LL-37 expression. Studies with a series of fatty acid derivatives with modifications in the aliphatic chain or carboxylic acid group yielded several analogs such as benzyl butyrate, trans-cinnamyl butyrate, glyceryl tributyrate, and phenethyl butyrate with a comparable LL-37-inducing activity to sodium butyrate. On the other hand, although reactive, the anhydride derivatives of short- and medium-chain fatty acids are as potent as their corresponding free acid forms in LL-37 induction. Thus, these newly identified free fatty acids and their analogs with a strong capacity to augment LL-37 synthesis may hold promise as immune boosting dietary supplements for antimicrobial therapy.

Keywords: AP-1; Butyrate; CBP; CRAMP; CREB; CREB-binding protein; Cathelicidins; DMSO; HDACi; HDP; Heptanoate; Hexanoate; Host defense peptides; LCFA; LL-37; MAPK; MCFA; SCFA; Short-chain fatty acids; activator protein 1; cAMP; cAMP response element-binding protein; cathelicidin-related antimicrobial peptide; cyclic adenosine monophosphate; dimethyl sulfoxide; hBD; hCAP18; histone deacetylase inhibitor; host defense peptide; human cationic antimicrobial peptide of 18kDa; human β-defensin; long-chain fatty acid; medium-chain fatty acid; mitogen-activated protein kinase; short-chain fatty acid.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Anti-Infective Agents / chemistry
  • Anti-Infective Agents / pharmacology*
  • Antimicrobial Cationic Peptides / agonists*
  • Antimicrobial Cationic Peptides / biosynthesis
  • Antimicrobial Cationic Peptides / genetics
  • Butyrates / chemistry
  • Butyrates / pharmacology*
  • Caproates / chemistry
  • Caproates / pharmacology
  • Cathelicidins
  • Cell Line, Tumor
  • Epithelial Cells / cytology
  • Epithelial Cells / drug effects*
  • Epithelial Cells / metabolism
  • Gene Expression / drug effects
  • Heptanoic Acids / chemistry
  • Heptanoic Acids / pharmacology
  • Humans
  • Immunologic Factors / chemistry
  • Immunologic Factors / pharmacology*
  • Monocytes / cytology
  • Monocytes / drug effects*
  • Monocytes / metabolism
  • Pentanoic Acids / chemistry
  • Pentanoic Acids / pharmacology
  • Structure-Activity Relationship

Substances

  • Anti-Infective Agents
  • Antimicrobial Cationic Peptides
  • Butyrates
  • Caproates
  • Heptanoic Acids
  • Immunologic Factors
  • Pentanoic Acids
  • hexanoic acid
  • n-pentanoic acid
  • Cathelicidins