Antiwrinkle and Antimelanogenesis Effects of Tyndallized Lactobacillus acidophilus KCCM12625P

Int J Mol Sci. 2020 Feb 27;21(5):1620. doi: 10.3390/ijms21051620.

Abstract

UVB irradiation can induce generation of reactive oxygen species (ROS) that cause skin aging or pigmentation. Lactobacillus acidophilus is a well-known probiotic strain that regulates skin health through antimicrobial peptides and organic products produced by metabolism and through immune responses. In this study, we investigated the antioxidative, antiwrinkle, and antimelanogenesis effects of tyndallized Lactobacillus acidophilus KCCM12625P (AL). To analyze the effects of AL on UV irradiation-induced skin wrinkle formation in vitro, human keratinocytes and human dermal fibroblasts were exposed to UVB. Subsequent treatment with AL induced antiwrinkle effects by regulating wrinkle-related genes such as matrix metalloproteinases (MMPs), SIRT-1, and type 1 procollagen (COL1AL). In addition, Western blotting assays confirmed that regulation of MMPs by AL in keratinocytes was due to regulation of the AP-1 signaling pathway. Furthermore, we confirmed the ability of AL to regulate melanogenesis in B16F10 murine melanoma cells treated with α-melanocyte-stimulating hormone (α-MSH). In particular, AL reduced the mRNA expression of melanogenesis-related genes such as tyrosinase, TYRP-1, and TYRP-2. Finally, we used Western blotting assays to confirm that the antimelanogenesis role of AL was due to its regulation of the cyclic adenosine monophosphate (cAMP) signaling pathway. Collectively, these results indicate that AL has an antiwrinkle activity in damaged skin and can inhibit melanogenesis. Thus, AL should be considered an important substance for potential use in anti-aging drugs or cosmetics.

Keywords: AP-1; Lactobacillus acidophilus; MMPs; antimelanogenesis; antiwrinkle.

MeSH terms

  • Animals
  • Cell Differentiation / drug effects
  • Cell Survival / drug effects
  • Cyclic AMP / metabolism
  • Fibroblasts / enzymology
  • Fibroblasts / metabolism
  • Fibroblasts / radiation effects*
  • Humans
  • Intramolecular Oxidoreductases / metabolism
  • Keratinocytes / enzymology
  • Keratinocytes / metabolism
  • Keratinocytes / radiation effects*
  • Lactobacillus acidophilus*
  • Matrix Metalloproteinases / genetics
  • Matrix Metalloproteinases / metabolism
  • Membrane Glycoproteins / metabolism
  • Mice
  • Monophenol Monooxygenase / metabolism
  • Oxidoreductases / metabolism
  • Probiotics*
  • Procollagen / genetics
  • Procollagen / metabolism
  • Reactive Oxygen Species / metabolism
  • Signal Transduction
  • Sirtuin 1 / genetics
  • Sirtuin 1 / metabolism
  • Skin / enzymology
  • Skin / radiation effects
  • Transcription Factor AP-1 / metabolism
  • Ultraviolet Rays* / adverse effects
  • alpha-MSH / pharmacology

Substances

  • Membrane Glycoproteins
  • Procollagen
  • Reactive Oxygen Species
  • Transcription Factor AP-1
  • alpha-MSH
  • Cyclic AMP
  • Oxidoreductases
  • Tyrp1 protein, mouse
  • Monophenol Monooxygenase
  • Matrix Metalloproteinases
  • Sirtuin 1
  • Intramolecular Oxidoreductases
  • dopachrome isomerase