152
Views
2
CrossRef citations to date
0
Altmetric
Articles

Study on the roles of melatonin in regulating dermal fibroblast growth in Liaoning cashmere goats by transcriptome sequencing

, , , , &

References

  • Yang Q, Dai S, Luo X, et al. Melatonin attenuates postovulatory oocyte dysfunction by regulating SIRT1 expression. Reproduction. 2018;156(1):81–92.
  • Fischer TW, Sweatman TW, Semak I, Sayre RM, Wortsman J, Slominski A. Constitutive and UV-induced metabolism of melatonin in keratinocytes and cell-free systems. Faseb J. 2006;20(9):1564–1566.
  • Yang CH, Xu JH, Ren QC, Duan T, Mo F, Zhang W. Melatonin promotes secondary hair follicle development of early postnatal cashmere goat and improves cashmere quantity and quality by enhancing antioxidant capacity and suppressing apoptosis. J Pineal Res. 2019;67(1):e12569.
  • Foldes A, Hoskinson RM, Baker P, McDonald BJ, Maxwell CA, Restall BJ. Effect of immunization against melatonin on seasonal fleece growth in feral goats. J Pineal Res. 1992;13(2):85–94.
  • Nixon AJ, Choy VJ, Parry AL, Pearson AJ. Fiber growth initiation in hair follicles of goats treated with melatonin. J Exp Zool. 1993;267(1):47–56.
  • Fischer TW, Burmeister G, Schmidt HW, Elsner P. Melatonin increases anagen hair rate in women with androgenetic alopecia or diffuse alopecia: results of a pilot randomized controlled trial. Br J Dermatol. 2004;150(2):341–345.
  • Ibraheem M, Galbraith H, Scaife J, Ewen S. Growth of secondary hair follicle of the Cashmere goat in vitro and their response to prolactin and melatonin. J Anatomy. 1994;185(1):135–142.
  • Fischer TW. [The influence of melatonin on hair physiology]. Hautarzt. 2009;60(12):962–972.
  • Kobayashi H, Kromminga A, Dunlop TW, et al. A role of melatonin in neuroectodermal-mesodermal interactions: the hair follicle synthesizes melatonin and expresses functional melatonin receptors. Faseb J. 2005;19(12):1710–1712.
  • Shen TNY, Kanazawa S, Kado M, et al. Interleukin-6 stimulates Akt and p38 MAPK phosphorylation and fibroblast migration in non-diabetic but not diabetic mice. PLOS One. 2017;12(5):e0178232.
  • Nelson AM, Katseff AS, Resnik SR, Ratliff TS, Zhu AS, Garza LA. Interleukin-6 null mice paradoxically display increased STAT3 activity and wound-induced hair neogenesis. J Invest Dermatol. 2016;136(5):1051–1053.
  • Tanabe A, Ogawa Y, Takemoto T, et al. Interleukin 6 induces the hair follicle growth phase (anagen). J Dermatol Sci. 2006;43(3):210–213.
  • Postlethwaite AE, Seyer JM. Stimulation of fibroblast chemotaxis by human recombinant tumor necrosis factor alpha (TNF-alpha) and a synthetic TNF-alpha 31-68 peptide. J Exp Med. 1990;172(6):1749–1756.
  • Abraham DJ, Shiwen X, Black CM, Sa S, Xu Y, Leask A. Tumor necrosis factor alpha suppresses the induction of connective tissue growth factor by transforming growth factor-beta in normal and scleroderma fibroblasts. J Biol Chem. 2000;275(20):15220–15225.
  • Noronha SM, Noronha SA, Klepp AG, Ipolito MZ, Ferreira LM, Gragnani A. Keratinocyte growth factor, interleukins (1 beta,6,8,10,12), and tumor necrosis factor alpha in culture medium of dermal fibroblast of burned patients. Acta Cir Bras. 2014;29(suppl 1):62–68.
  • Wang X, Chen H, Tian R, et al. Macrophages induce AKT/β-catenin-dependent Lgr5+ stem cell activation and hair follicle regeneration through TNF. Nat Commun. 2017;8:14091.
  • Laurikkala J, Pispa J, Jung HS, et al. Regulation of hair follicle development by the TNF signal ectodysplasin and its receptor Edar. Development. 2002;129(10):2541–2553.
  • Fukata M, Vamadevan AS, Abreu MT. Toll-like receptors (TLRs) and Nod-like receptors (NLRs) in inflammatory disorders. Semin Immunol. 2009;21(4):242–253.
  • Gilon M, Sher N, Cohen S, Gat U. Transcriptional activation of a subset of hair keratin genes by the NF-kappaB effector p65/RelA. Differentiation. 2008;76(5):518–530.
  • Schmidt-Ullrich R, Aebischer T, Hülsken J, Birchmeier W, Klemm U, Scheidereit C. Requirement of NF-kappaB/Rel for the development of hair follicles and other epidermal appendices. Development. 2001;128(19):3843–3853.
  • Kloepper JE, Ernst N, Krieger K, et al. NF-κB activity is required for anagen maintenance in human hair follicles in vitro. J Invest Dermatol. 2014;134(7):2036–2038.
  • Rosenstiel P, Fantini M, Bräutigam K, et al. TNF-alpha and IFN-gamma regulate the expression of the NOD2 (CARD15) gene in human intestinal epithelial cells. Gastroenterology. 2003;124(4):1001–1009.
  • Onphachanh X, Lee HJ, Lim JR, et al. Enhancement of high glucose-induced PINK1 expression by melatonin stimulates neuronal cell survival: involvement of MT2/Akt/NF-κB pathway. J Pineal Res. 2017;63(2):1–17.
  • Hou J, Ma T, Cao H, et al. TNF-α-induced NF-κB activation promotes myofibroblast differentiation of LR-MSCs and exacerbates bleomycin-induced pulmonary fibrosis. J Cell Physiol. 2018;233(3):2409–2419.
  • Kulski JK, Shiina T, Anzai T, Kohara S, Inoko H. Comparative genomic analysis of the MHC: the evolution of class I duplication blocks, diversity and complexity from shark to man. Immunol Rev. 2002;190:95–122.
  • Ware CF. Network communications: lymphotoxins, light, and TNF. Annu Rev Immunol. 2005;23:787–819.
  • Hwu WL, Yang CF, Fann CS, et al. Mapping of psoriasis to 17q terminus. J Med Genet. 2005;42(2):152–158.
  • Jacques VS. Interleukin-6: an overview. Annu Rev Immunol. 1990;8:253–278.
  • Vyas D, Lopez-Hisijos N, Shah P, et al. A second-generation proteasome inhibitor and doxorubicin modulates IL-6, pSTAT-3 and NF-kB activity in MDA-MB-231 breast cancer cells. J Nanosci Nanotechnol. 2017;17(1):175–185.
  • Toker H, Görgün EP, Korkmaz EM. Analysis of IL-6, IL-10 and NF-κB gene polymorphisms in aggressive and chronic periodontitis. Cent Eur J Public Health. 2017;25(2):157–162.
  • Hsu EC, Kulp SK, Huang HL, et al. Integrin-linked kinase as a novel molecular switch of the IL-6-NF-κB signaling loop in breast cancer. Carcinogenesis. 2016;37(4):430–442.
  • Chen Z, Li YX, Fu HJ, et al. Hepatitis B virus core antigen stimulates il-6 expression via p38, ERK and NF-κB pathways in hepatocytes. Cell Physiol Biochem. 2017;41(1):91–100.
  • Speranskii AI, Kostyuk SV, Kalashnikova EA, Veiko NN. [Enrichment of extracellular DNA from the cultivation medium of human peripheral blood mononuclears with genomic CpG rich fragments results in increased cell production of IL-6 and TNF-a via activation of the NF-kB signaling pathway]. Biomed Khim. 2016;62(3):331–340.
  • Sanchavanakit N, Saengtong W, Manokawinchoke J, Pavasant P. TNF-α stimulates MMP-3 production via PGE2 signalling through the NF-kB and p38 MAPK pathway in a murine cementoblast cell line. Arch Oral Biol. 2015;60(7):1066–1074.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.