Literature DB >> 26738491

Color reduction of melanin by lysosomal and peroxisomal enzymes isolated from mammalian cells.

Dong Jun Park1, Simranjeet Singh Sekhon2, Jihee Yoon3, Yang-Hoon Kim4, Jiho Min5,6.   

Abstract

Lysosomes and peroxisomes are organelles with many functions in all eukaryotic cells. Lysosomes contain hydrolytic enzymes (lysozyme) that degrade molecules, whereas peroxisomes contain enzymes such as catalase that convert hydrogen peroxide (H2O2) to water and oxygen and neutralize toxicity. In contrast, melanin is known as a helpful element to protect the skin against harmful ultraviolet rays. However, a high quantity of melanin leads to hyperpigmentation or skin cancer in human. New materials have already been discovered to inhibit tyrosinase in melanogenesis; however, melanin reduction does not suggest their preparation. In this study, we report that the color intensity because of melanin decreased by the cellular activation of lysosomes and peroxisomes. An increase in the superficial intensity of lysosome and peroxisome activities of HeLa cells was observed. In addition, a decrease in the amount of melanin has also been observed in mammalian cells without using any other chemical, showing that the process can work in vivo for treating melanin. Therefore, the results of this study indicate that the amount of melanin decreases by the lysosome and peroxisome activity after entering the cells, and functional organelles are effective in color reduction. This mechanism can be used in vivo for treating melanin.

Entities:  

Keywords:  Degradation; Lysosomes; Melanin; Peroxisomes; Reactive oxygen species (ROS)

Mesh:

Substances:

Year:  2016        PMID: 26738491     DOI: 10.1007/s11010-015-2645-2

Source DB:  PubMed          Journal:  Mol Cell Biochem        ISSN: 0300-8177            Impact factor:   3.396


  23 in total

1.  Melanogenesis and melanoma.

Authors:  Patrick A Riley
Journal:  Pigment Cell Res       Date:  2003-10

2.  Inhibitors of mammalian melanocyte tyrosinase: in vitro comparisons of alkyl esters of gentisic acid with other putative inhibitors.

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Journal:  Biochem Pharmacol       Date:  1999-03-15       Impact factor: 5.858

3.  Inhibitory effects of Sargassum polycystum on tyrosinase activity and melanin formation in B16F10 murine melanoma cells.

Authors:  Y Y Chan; K H Kim; S H Cheah
Journal:  J Ethnopharmacol       Date:  2011-07-26       Impact factor: 4.360

4.  Melanogenesis in transfected fibroblasts induces lysosomal activation.

Authors:  J Borovanský; A M Mommaas; N P Smit; D Eygendaal; A J Winder; B J Vermeer; S Pavel
Journal:  Arch Dermatol Res       Date:  1997-02       Impact factor: 3.017

Review 5.  Peroxisomes and oxidative stress.

Authors:  Michael Schrader; H Dariush Fahimi
Journal:  Biochim Biophys Acta       Date:  2006-09-14

6.  Increased in vitro lysosomal function in oxidative stress-induced cell lines.

Authors:  Jihee Yoon; Seung Hyuck Bang; Jin-Soo Park; Suk-Tai Chang; Yang-Hoon Kim; Jiho Min
Journal:  Appl Biochem Biotechnol       Date:  2010-10-16       Impact factor: 2.926

7.  Melanin endocytosis by cultured mammalian cells. A model for melanin in a cellular environment.

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Journal:  Exp Cell Res       Date:  1983-12       Impact factor: 3.905

8.  Characterization of antimicrobial activity of the lysosomes isolated from Saccharomyces cerevisiae.

Authors:  Jihee Yoon; Jae-Min Park; Seung-Ki Jung; Keun-Young Kim; Yang-Hoon Kim; Jiho Min
Journal:  Curr Microbiol       Date:  2009-03-25       Impact factor: 2.188

Review 9.  Tyrosinase and related proteins in mammalian pigmentation.

Authors:  V del Marmol; F Beermann
Journal:  FEBS Lett       Date:  1996-03-04       Impact factor: 4.124

Review 10.  Peroxisomes and peroxisomal disorders: the main facts.

Authors:  Marco Fidaleo
Journal:  Exp Toxicol Pathol       Date:  2009-09-09
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  1 in total

Review 1.  Skin Pigmentation Abnormalities and Their Possible Relationship with Skin Aging.

Authors:  Ai-Young Lee
Journal:  Int J Mol Sci       Date:  2021-04-02       Impact factor: 5.923

  1 in total

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