Involvement of DKK1 secreted from adipose-derived stem cells in alopecia areata

  • Nahyun Choi 1 ,
  • Juyeong Hwang 1 ,
  • Doo Yeong Kim 2 ,
  • Jino Kim 3 ,
  • Seung Yong Song 4 ,
  • Jong-Hyuk Sung , 1,2
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  • 1. Epi Biotech Co., Ltd., Incheon, South Korea
  • 2. College of Pharmacy, Yonsei Institute of Pharmaceutical Sciences, Yonsei University, Incheon, South Korea
  • 3. New Hair Plastic Surgery Clinic, Seoul, South Korea
  • 4. Institute for Human Tissue Restoration, Department of Plastic and Reconstructive Surgery, Yonsei University College of Medicine, Seoul, South Korea
brian99@yonsei.ac.kr

Received date: 04 Jul 2023

Revised date: 11 Sep 2023

Accepted date: 10 Oct 2023

Copyright

2023 2023 The Authors. Cell Proliferation published by Beijing Institute for Stem Cell and Regenerative Medicine and John Wiley & Sons Ltd.

Abstract

Adipose-derived stem cells (ASCs) have shown efficacy in promoting hair growth, while DKK1 inhibits the WNT pathway, which is associated with hair loss. Our study focused on investigating the expression of DKK1 in alopecia areata (AA), a condition characterised by significant increases in the DKK1 levels in human and mouse ASCs. Treatment of interferon-γ increased the expression of DKK1 via STAT3 phosphorylation in ASCs. Treatment with recombinant DKK1 resulted in a decrease of cell growth in outer root sheath cells, whereas the use of a DKK1 neutralising antibody promoted hair growth. These results indicate that ASCs secrete DKK1, playing a crucial role in the progression and development of AA. Consequently, we generated DKK1 knockout (KO) ASCs using the Crispr/Cas9 system and evaluated their hair growth-promoting effects in an AA model. The DKK1 KO in ASCs led to enhanced cell motility and reduced cellular senescence by activating the WNT signalling pathway, while it reduced the expression of inflammatory cytokines by inactivating the NF-kB pathway. As expected, the intravenous injection of DKK1-KO-ASCs in AA mice, and the treatment with a conditioned medium derived from DKK1-KO-ASCs in hair organ culture proved to be more effective compared with the use of naïve ASCs and their conditioned medium. Overall, these findings suggest that DKK1 represents a novel therapeutic target for treating AA, and cell therapy using DKK1-KO-ASCs demonstrates greater efficiency.

Cite this article

Nahyun Choi , Juyeong Hwang , Doo Yeong Kim , Jino Kim , Seung Yong Song , Jong-Hyuk Sung . Involvement of DKK1 secreted from adipose-derived stem cells in alopecia areata[J]. Cell Proliferation, 2024 , 57(3) : e13562 . DOI: 10.1111/cpr.13562

1
Sung JH. Effective and economical cell therapy for hair regeneration. Biomed Pharmacother. 2023;157:113988.

2
Won CH, Park GH, Wu X, et al. The basic mechanism of hair growth stimulation by adipose-derived stem cells and their secretory factors. Curr Stem Cell Res Ther. 2017;12(7):535-543.

3
Rehman J, Traktuev D, Li J, et al. Secretion of angiogenic and antiapoptotic factors by human adipose stromal cells. Circulation. 2004;109(10):1292-1298.

4
Hassan WU, Greiser U, Wang W. Role of adipose-derived stem cells in wound healing. Wound Repair Regen. 2014;22(3):313-325.

5
Choi N, Shin S, Song SU, Sung JH. Minoxidil promotes hair growth through stimulation of growth factor release from adipose-derived stem cells. Int J Mol Sci. 2018;19(3):691.

6
Choi N, Kim W-S, Oh SH, Sung JH. Epiregulin promotes hair growth via EGFR-medicated epidermal and ErbB4-mediated dermal stimulation. Cell Prolif. 2020;53(9):e12881.

7
Choi N, Sung JH. Udenafil induces the hair growth effect of adipose-derived stem cells. Biomol Ther. 2019;27(4):404-413.

8
Jeong YM, Sung YK, Kim W-K, et al. Ultraviolet B preconditioning enhances the hair growth-promoting effects of adipose-derived stem cells via generation of reactive oxygen species. Stem Cells Dev. 2013;22:158-168.

9
Kim JH, Kim WK, Sung YK, et al. The molecular mechanism underlying the proliferating and preconditioning effect of vitamin C on adipose-derived stem cells. Stem Cells Dev. 2014;23:1364-1376.

10
Kim JI, Gyu Park S, Kim W-K, et al. Functional regulation of adipose-derived stem cells by PDGF-D. Stem Cells. 2015;33:542-556.

11
Yang Y, Choi H, Seon M, Cho D, Bang SI. LL-37 stimulates the functions of adipose-derived stromal/stem cells via early growth response 1 and the MAPK pathway. Stem Cell Res Ther. 2016;7:58.

12
Choi N, Choi J, Kim JH. Generation of trichogenic adipose-derived stem cells by expression of three factors. J Dermatol Sci. 2018;92(1):18-29.

13
Anderi R, Makdissy N, Azar A, Rizk F, Hamade A. Cellular therapy with human autologous adipose-derived adult cells of stromal vascular fraction for alopecia areata. Stem Cell Res Ther. 2018;9(1):141.

14
Lee SB, Shin HT, Byun JW, Shin J, Choi GS. Clinical efficacy of adipocyte-derived stem cells conditioned media combined with micro-injury in refractory patch of alopecia areata. Arch Dermatol Res. 2022;314:527-532.

15
Semënov MV, Tamai K, Brott BK, Kühl M, Sokol S, He X. Head inducer Dickkopf-1 is a ligand for Wnt coreceptor LRP6. Curr Biol. 2001;11(12):951-961.

16
Lei M, Guo H, Qiu W, et al. Modulating hair follicle size with Wnt10b/DKK1 during hair regeneration. Exp Dermatol. 2014;23(6):407-413.

17
Kwack MH, Kim MK, Kim JC, Sung YK. Dickkopf 1 promotes regression of hair follicles. J Invest Dermatol. 2012;132(6):1554-1560.

18
Kwack MH, Sung YK, Chung EJ, et al. Dihydrotestosterone-inducible dickkopf 1 from balding dermal papilla cells causes apoptosis in follicular keratinocytes. J Invest Dermatol. 2008;128(2):262-926.

19
Kwack MH, Lee JH, Seo CH, Kim JC, Kim MK, Sung YK. Dickkopf-1 is involved in dexamethasone-mediated hair follicle regression. Exp Dermatol. 2017;26(10):952-954.

20
Fawzi M, Mahmoud SB, Shaker OG, et al. Assessment of tissue levels of dickkopf-1 in androgenetic alopecia and alopecia areata. J Cosmet Dermatol. 2015;15:10-15.

21
Mahmoud EA, Elgarhy LH, Hasby EA, Mohammad L. Dickkopf-1 expression in androgenetic alopecia and alopecia areata in male patients. Am J Dermatopathol. 2019;41:122-127.

22
Yi Y, Kim WK, Choi JS, et al. Isolation of adipose-derived stem cells by using a sub-fractionation culturing method. Expert Opin Biol Ther. 2014;14(11):1551-1560.

23
Wang EH, McElwee KJ. Induction of alopecia areata in C3H/HeJ mice via cultured cell transfer. Protoc Exch. 2014.

DOI

24
Shin JM, Choi DJ, Sohn KC, et al. Induction of alopecia areata in C3H/HeJ mice using polyinosinic-polycytidylic acid (poly[I:C]) and interferon-gamma. Sci Rep. 2018;8:12518.

25
Gonzalez GR, Shook BA, Andrae J, et al. Skin adipocyte stem cell self-renewal is regulated by a PDGFA/AKT-signaling axis. Cell Stem Cell. 2016;19(6):738-751.

26
Lensing M, Jabbari A. An overview of JAK/STAT pathways and JAK inhibition in alopecia areata. Front Immunol. 2022;13:955035.

27
Li W, Henderson LJ, Eugene O. Major et al, IFN-γ mediates enhancement of HIV replication in astrocytes by inducing an antagonist of the β-catenin pathway (DKK1) in a STAT 3-dependent manner. J Immunol. 2011;186(12):6771-6778.

28
Lee YJ, Park SH, Park HR, Lee Y, Kang H, Kim JE. Mesenchymal stem cells antagonize IFN-induced proinflammatory changes and growth inhibition effects via Wnt/β-Catenin and JAK/STAT pathway in human outer root sheath cells and hair follicles. Int J Mol Sci. 2021;22(9):4581.

29
Chae WJ, Bothwell ALM. Dickkopf1: an immunomodulatory ligand and Wnt antagonist in pathological inflammation. Differentiation. 2019;108:33-39.

30
Ryu S, Lee Y, Hyun MY, et al. Mycophenolate antagonizes IFN-γ-induced catagen-like changes via β-catenin activation in human dermal papilla cells and hair follicles. Int J Mol Sci. 2014;15(9):16800-16815.

31
Gilhar A, Landau M, Assy B, Shalaginov R, Serafimovich S, Kalish RS. Mediation of alopecia areata by cooperation between CD4+ and CD8+ T lymphocytes transfer to human scalp explants on prkdcscid mice. Arch Dermatol. 2002;138(7):916-922.

32
Gustafson B, Smith U. The WNT inhibitor Dickkopf 1 and bone morphogenetic protein 4 rescue adipogenesis in hypertrophic obesity in humans. Diabetes. 2012;61(5):1217-1224.

33
Christodoulides C, Laudes M, Cawthorn WP, et al. The Wnt antagonist Dickkopf-1 and its receptors are coordinately regulated during early human adipogenesis. J Cell Sci. 2006;119(12):2613-2620.

34
Kato T, Khanh VC, Sato K. Elevated expression of Dkk-1 by glucocorticoid treatment impairs bone regenerative capacity of adipose tissue-derived mesenchymal stem cells. Stem Cells Dev. 2018;27(2):85-99.

35
Hie M, Iitsuka N, Otsuka T, Tsukamoto I. Insulin-dependent diabetes mellitus decreases osteoblastogenesis associated with the inhibition of Wnt signaling through increased expression of Sost and Dkk1 and inhibition of Akt activation. Int J Mol Med. 2011;28(3):455-462.

36
Chae WJ, Ehrlich AK, Chan PY, et al. The Wnt antagonist Dickkopf-1 promotes pathological type 2 cell-mediated inflammation. Immunity. 2016;44(2):246-258.

37
Yeremenko N, Zwerina K, Rigter G, et al. Tumor necrosis factor and interleukin-6 differentially regulate Dkk-1 in the inflamed arthritic joint. Arthritis Rheumatol. 2015;67(8):2071-2075.

38
Yamaguchi Y, Morita A, Maeda A, et al. Regulation of skin pigmentation and thickness by Dickkopf 1 (DKK1). J Invest Dermatol. 2009;14(1):73-75.

39
Abashima K, Sakabe J, Yoshiki R, et al. Involvement of Wnt signaling in dermal fibroblasts. Am J Pathol. 2010;176(2):721-732.

40
Giuliano CJ, Lin A, Girish V, Sheltzer JM. Generating single cell-derived knockout clones in mammalian cells with CRISPR/Cas9. Curr Protoc Mol Biol. 2019;128(1):e100.

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