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Transcriptomic Analysis Reveals Wound Healing of Morus alba Root Extract by Up-Regulating Keratin Filament and CXCL12/CXCR4 Signaling

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Title
Transcriptomic Analysis Reveals Wound Healing of Morus alba Root Extract by Up-Regulating Keratin Filament and CXCL12/CXCR4 Signaling
Issued Date
2015-08
Citation
Phytotherapy Research, v.29, no.8, pp.1251 - 1258
Type
Article
Author Keywords
Morus alba root ; therapeutic treatment ; C-X-C motif chemokine 12 (CXCL12) ; chemokine receptor 4 (CXCR4)
Keywords
Animal ; Animal Cell ; Animal Experiment ; Animal Model ; Animals ; APOPTOSIS ; Article ; C-X-C Motif Chemokine 12 (CXCL12) ; Cell Cycle ; Cell Differentiation ; Cell Growth ; Cell Line ; Cell Migration ; Cell Proliferation ; Cell Viability ; CELLS ; Chemistry ; Chemokine CXCL12 ; Chemokine Receptor 4 (CXCR4) ; Chemokine Receptor CXCR4 ; CHemOKINE RECEPTORS ; Controlled Study ; CXCL12 Protein, Mouse ; CXCR4 Protein, Mouse ; Cytokeratin 14 ; Cytokeratin 6 ; Cytokeratin 6A ; Cytology ; Down Regulation ; Drug Effects ; Drug Efficacy ; Drug Mechanism ; DYNAMICS ; Extracellular Matrix ; HAIR FOLLICLE ; Immune Response ; In Vitro Study ; In Vitro Techniques ; Institute For Cancer Research Mouse ; INTERMEDIATE-FILAMENTS ; Keratin ; Keratinocyte ; Keratinocytes ; Keratins ; Lipid Metabolism ; Messenger RNA ; Metabolism ; Mice ; Mice, Inbred ICR ; Morus ; Morus Alba ; Morus Alba Root ; Mouse ; Mulberry Extract ; Nonhuman ; Plant Extract ; Plant Extracts ; Plant Root ; Plant Roots ; Primary Cell Culture ; Protein Expression ; Protein Function ; Receptors, CXCR4 ; REGENERATION ; RNA, Messenger ; Signal Transduction ; Skin ; SMALL GTPASES ; Stromal Cell Derived Factor 1 ; Therapeutic Treatment ; Transcriptome ; Unclassified Drug ; Up-Regulation ; Wound Healing
ISSN
0951-418X
Abstract

Facilitation of the wound healing process is important because a prolonged wound site increases pain and the risk of infection. In oriental medicine, an extract of Morus alba root (MA) has usually been prescribed as traditional treatment for accelerating wound healing, and it has been proven to be safe for centuries. To study the molecular mechanism of MA-mediated skin wound healing, we performed a primary cell culture and a skin explant culture and observed significant difference between the groups with and without MA extract. In the cellular system, a real-time cell analysis and real-time quantitative PCR were performed. It was found that MA extract enhanced proliferation in a dose-dependent manner on Kera-308 cell line, and up-regulated keratin expression including wound-induced Krt6a. In skin explant culture, the mRNA level derived from cell outgrowth displayed a tendency toward more up-regulated mRNA associated keratin filaments and toward a more up-regulated mRNA level of C-X-C motif chemokine 12 (CXCL12) and a chemokine receptor 4 (CXCR4) axis signaling pathway downstream. In this process, we concluded that MA extract had a scientific possibility of wound repair by increasing intracellular and extracellular supports and by inducing a CXCL12/CXCR4 signaling pathway. © 2015 John Wiley & Sons, Ltd.

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URI
http://hdl.handle.net/20.500.11750/5179
DOI
10.1002/ptr.5375
Publisher
Wiley
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이창훈
Lee, Chang-Hun이창훈

Department of New Biology

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