All-trans retinoic acid prevents oxidative stress-mediated cellular senescence via upregulation of insulin-like growth factor binding protein-6 in normal human epidermal keratinocytes

Authors

DOI:

https://doi.org/10.2298/ABS210615036C

Keywords:

ATRA, IGFBP-6, cellular senescence, ROS, NHEK

Abstract

Paper description:

  • Potential mechanisms of action of all-trans retinoic acid (ATRA) in primary normal human epidermal keratinocytes (NHEKs) were examined.
  • Microarray analysis using ATRA-treated NHEKs, insulin-like growth factor binding protein-6 (IGFBP-6) gene overexpression and knockdown systems, senescence-associated (SA)-β-galactosidase (Gal) staining, real-time PCR, Western blotting were performed.
  • ATRA increased IGFBP-6 expression in NHEKs. IGFBP-6 / ATRA prevents H2O2-induced premature senescence (assessed by SA-β-Gal and p21) in
  • ATRA ameliorates premature senescence in NHEKs at least partly via an IGFBP-6-dependent pathway.

Abstract: All-trans retinoic acid (ATRA) influences cellular proliferation and differentiation but its mechanisms of action are not understood in keratinocytes. To investigate the potential mechanisms of action of ATRA in keratinocytes, microarray analysis of ATRA-treated normal human epidermal keratinocytes (NHEKs) was performed. Based on microarray data, we focused on insulin-like growth factor binding protein-6 (IGFBP-6), which is known to inhibit cellular senescence but has not been previously investigated in the context of ATRA-induced signaling in NHEKs. We verified that ATRA significantly increased IGFBP-6 gene and protein expression in NHEKs. Next, the effects of ATRA and IGFBP-6 on cell proliferation and senescence in H2O2-treated NHEKs were examined. IGFBP-6 was knocked-down using siRNA or overexpressed using pCMV-IGFBP-6. Cellular proliferation was observed using the bromodeoxyuridine (BrdU) incorporation assay. Cellular senescence was determined by monitoring SA-β-Gal staining and p21 expression. When IGFBP-6 was knocked down, cellular proliferation was inhibited, and the cellular senescence markers were increased. IGFBP-6 overexpression or ATRA treatment of H2O2-treated NHEKs rescued these effects. Taken together, our results suggest that ATRA prevents premature senescence-related skin damage at least in part by increasing IGFBP-6 expression, as shown herein in reactive oxygen species (ROS)-stimulated NHEKs.

Downloads

Download data is not yet available.

Author Biography

Hyangtae Choi, 1. Department of Dermatology, Chung-Ang University College of Medicine, Seoul, Republic of Korea; 2. Department of Medicine, Graduate School, Chung-Ang University, Seoul, Republic of Korea; 3.Basic Research & Innovation Division, Amorepacific Corp. R&D Unit, Yongin, Republic of Korea

Senior Researcher in R & D center

References

Mukherjee S, Date A, Patravale V, Korting H, Roeder A, Weindl G. Retinoids in the treatment of skin aging: an overview of clinical efficacy and safety. Clin Interv Aging. 2006;1(4):327-48. https://doi.org/10.2147/ciia.2006.1.4.327

Rinnerthaler M, Bischof J, Streubel MK, Trost A, Richter K. Oxidative stress in aging human skin. Biomolecules. 2015;5(2):545-89. https://doi.org/10.3390/biom5020545

Micutkova L, Diener T, Li C, Wrzesinska A, Mueck C, Heutter E, Weinberger B, Loebenstein B, Roepstorff P, Zeng R, Duerr P. Insulin-like growth factor binding protein-6 delays replicative senescence of human fibroblasts. Mech Ageing Dev. 2011;132(10):468-79. https://doi.org/10.1016/j.mad.2011.07.005

Schroeder M, Zouboulis CC. All-trans-retinoic acid and 13-cis-retinoic acid: pharmacokinetics and biological activity in different cell culture models of human keratinocytes. Horm Metab Res. 2007;39(2):136-40. https://doi.org/10.1055/s-2007-961813

Jean J, Soucy J, Pouliot R. Effects of retinoic acid on keratinocyte proliferation and differentiation in a psoriatic skin model. Tissue Eng Part A. 2011;17(13-14):1859-68. https://doi.org/10.1089/ten.tea.2010.0463

Min BM, Oh JE, Choi CM. Retinoic acid delays keratinocyte senescence by suppression of betaig-h3 and p16 expression and induction of telomerase activity. Int J Mol Med. 2004;13(1):25-31. https://doi.org/10.3892/ijmm.13.1.25

Fujishita K, Koizumi S, Inoue K. Upregulation of P2Y2 receptors by retinoids in normal human epidermal keratinocytes. Purinergic Signal. 2006;2(3):491-8. https://doi.org/10.1007/s11302-005-7331-5

Krtolica A, Parrinello S, Lockett S, Desprez PY, Campisi J. Senescent fibroblasts promote epithelial cell growth and tumorigenesis: a link between cancer and aging. Proc Natl Acad Sci USA. 2001;98(21):12072-7. https://doi.org/10.1073/pnas.211053698

Bach LA. IGFBP-6 five years on; not so 'forgotten'? Growth Horm IGF Res. 2005;15(3):185-92. https://doi.org/10.1016/j.ghir.2005.04.001

Firth SM, Baxter RC. Cellular actions of the insulin-like growth factor binding proteins. Endocr Rev. 2002;23(6):824-54. https://doi.org/10.1210/er.2001-0033

Xie L, Tsaprailis G, Chen QM. Proteomic identification of insulin-like growth factor-binding protein-6 induced by sublethal H2O2 stress from human diploid fibroblasts. Mol Cell Proteomics. 2005;4(9):1273-83. https://doi.org/10.1074/mcp.M500032-MCP200

Beilharz EJ, Russo VC, Butler G, Baker NL, Connor B, Sirimanne ES, Dragunow M, Werther GA, Gluckman PD, Williams CE, Scheepens A. Co-ordinated and cellular specific induction of the components of the IGF/IGFBP axis in the rat brain following hypoxic-ischemic injury. Brain Res Mol Brain Res. 1998;59(2):119-34. https://doi.org/10.1016/S0169-328X(98)00122-3

Kato M, Ishizaki A, Hellman U, Wernstedt C, Kyogoku M, Miyazono K, Heldin CH, Funa K. A human keratinocyte cell line produces two autocrine growth inhibitors, transforming growth factor-beta and insulin-like growth factor binding protein-6, in a calcium- and cell density-dependent manner. J Biol Chem. 1995;270(21):12373-9. https://doi.org/10.1074/jbc.270.21.12373

Marinaro JA, Hendrich EC, Leeding KS, Bach LA. HaCaT human keratinocytes express IGF-II, IGFBP-6, and an acid-activated protease with activity against IGFBP-6. Am J Physiol. 1999;276(3):E536-42. https://doi.org/10.1152/ajpendo.1999.276.3.E536

Ksiazek K. A comprehensive review on mesenchymal stem cell growth and senescence. Rejuvenation Res. 2009;12(2):105-16. https://doi.org/10.1089/rej.2009.0830

Wei H, Li Z, Hu S, Chen X, Cong X. Apoptosis of mesenchymal stem cells induced by hydrogen peroxide concerns both endoplasmic reticulum stress and mitochondrial death pathway through regulation of caspases, p38 and JNK. J Cell Biochem. 2010;111(4):967-78. https://doi.org/10.1002/jcb.22785

Ho PJ, Yen ML, Tang BC, Chen CT, Yen B. H2O2 accumulation mediates differentiation capacity alteration, but not proliferative decline, in senescent human fetal mesenchymal stem cells. Antioxid Redox Signal. 2013;18(15):1895-905. https://doi.org/10.1089/ars.2012.4692

Burova E, Borodkina A, Shatrova A, Nikolsky N. Sublethal oxidative stress induces the premature senescence of human mesenchymal stem cells derived from endometrium. Oxid Med Cell Longev. 2013;2013:474931. https://doi.org/10.1155/2013/474931

Thuringer JM, Katzberg AA. The effect of age on mitosis in the human epidermis. J Invest Dermatol. 1959;33:35-9. https://doi.org/10.1038/jid.1959.119

West MD. The cellular and molecular biology of skin aging. Arch Dermatol. 1994;130(1):87-95. https://doi.org/10.1001/archderm.1994.01690010091014

Pelle E, Huang X, Mammone T, Marenus K, Maes D, Frenkel K. Ultraviolet-B-induced oxidative DNA base damage in primary normal human epidermal keratinocytes and inhibition by a hydroxyl radical scavenger. J Invest Dermatol. 2003;121(1):177-83. https://doi.org/10.1046/j.1523-1747.2003.12330.x

Campisi J, d'Adda di Fagagna F. Cellular senescence: when bad things happen to good cells. Nat Rev Mol Cell Biol. 2007;8(9):729-40. https://doi.org/10.1038/nrm2233

Gabbitas B, Canalis E. Retinoic acid regulates the expression of insulin-like growth factors I and II in osteoblasts. J Cell Physiol. 1997;172(2):253-64. https://doi.org/10.1002/(SICI)1097-4652(199708)172:2<253::AID-JCP12>3.0.CO;2-A

Martin JL, Coverley JA, Pattison ST, Baxter R. Insulin-like growth factor-binding protein-3 production by MCF-7 breast cancer cells: stimulation by retinoic acid and cyclic adenosine monophosphate and differential effects of estradiol. Endocrinology 1995;136(3):1219-26. https://doi.org/10.1210/endo.136.3.7532580

Babajko S, Binoux M. Modulation by retinoic acid of insulin-like growth factor (IGF) and IGF binding protein expression in human SK-N-SH neuroblastoma cells. Eur J Endocrinol. 1996;134(4):474-80. https://doi.org/10.1530/eje.0.1340474

Forman HJ. Use and abuse of exogenous H2O2 in studies of signal transduction. Free Radic Biol Med. 2007;42(7):926-32. https://doi.org/10.1016/j.freeradbiomed.2007.01.011

Lu T, Finkel T. Free radicals and senescence. Exp Cell Res. 2008;314(9):1918-22. https://doi.org/10.1016/j.yexcr.2008.01.011

Passos JF, Von Zglinicki T. Oxygen free radicals in cell senescence: are they signal transducers? Free Radic Res. 2006;40(12):1277-83. https://doi.org/10.1080/10715760600917151

Toussaint O, Medrano EE, von Zglinicki T. Cellular and molecular mechanisms of stress-induced premature senescence (SIPS) of human diploid fibroblasts and melanocytes. Exp Gerontol. 2000;35(8): 927-45. https://doi.org/10.1016/S0531-5565(00)00180-7

Downloads

Published

2021-10-12

How to Cite

1.
Choi H, Lee JY, Park NH, Nam J, Park W- seok, Lee CS, Kim BJ. All-trans retinoic acid prevents oxidative stress-mediated cellular senescence via upregulation of insulin-like growth factor binding protein-6 in normal human epidermal keratinocytes. Arch Biol Sci [Internet]. 2021Oct.12 [cited 2024Dec.3];73(3):425-32. Available from: https://serbiosoc.org.rs/arch/index.php/abs/article/view/6698

Issue

Section

Articles