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Series GSE69501 Query DataSets for GSE69501
Status Public on Jun 03, 2017
Title FGF18 Signaling for Hair Cycle Resting Phase Determines Radioresistance of Hair Follicles by the Arrest of Hair Cycling
Organism Mus musculus
Experiment type Expression profiling by array
Summary Telogen (resting phase) hair follicles are more radioresistant than anagen (growth phase) ones. Irradiation of BALB/c mice in the anagen phase with γ-rays at 6 Gy induced hair follicle dystrophy, whereas irradiation in the telogen phase induced the arrest of hair follicle elongation without any dystrophy after post-irradiation depilation. In contrast, FGF18 was highly expressed in the telogen hair follicles to maintain the telogen phase and also the quiescence of hair follicle stem cells. Therefore, the inhibition of FGF receptor signaling at telogen induced the dystrophy after post-irradiation depilation. In addition, the administration of recombinant FGF18 suppressed cell proliferation in the hair follicles and enhanced the repair of radiation-induced DNA damage, so FGF18 protected the anagen hair follicles against radiation damage to enhance hair regeneration. Moreover, FGF18 reduced the expression of cyclin B1 and cdc2 in the skin and FGF18 signaling induced G2/M arrest in the keratinocyte cell line HaCaT, although no obvious change of the expression of DNA repair genes was detected by DNA microarray analysis. These findings suggest that FGF18 signaling for the hair cycle resting phase causes radioresistance in telogen hair follicles by arresting the proliferation of hair follicle cells.
 
Overall design Portions of dorsal skin of 7-week-old male BALB/c mice were depilated to induce anagen phase of hair follicles. One hundred micrograms of FGF18 diluted in saline containing 5 μg/μl heparin was administered intraperitoneally to mice 6 days after depilation, and then mice were subjected to total body irradiation with γ-rays at 6 Gy 24 h after FGF administration. The skin was removed from treated mice 4 h after irradiation and total RNAs were isolated from the skin. The mRNA expression profiles were obtained using Affymetrix GeneChip Mouse Gene 2.0 ST Array (Affymetrix, Santa Clara, CA, USA).
 
Contributor(s) Nakayama F, Umeda S, Yasuda T, Kawano M, Fujita M, Ishikawa A, Imamura T, Imai T
Citation(s) 28740887
Submission date Jun 03, 2015
Last update date May 01, 2018
Contact name Atsuko Ishikawa
Organization name National Institute of Radiologocal Sciences
Department Research Center for Charged Particle Therapy
Lab RadGenomics Project
Street address Anagawa 4-9-1
City Chiba
State/province Chiba
ZIP/Postal code 2638555
Country Japan
 
Platforms (1)
GPL16570 [MoGene-2_0-st] Affymetrix Mouse Gene 2.0 ST Array [transcript (gene) version]
Samples (2)
GSM1702069 141106_12IR-01
GSM1702070 141106_12IR-02
Relations
BioProject PRJNA285743

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE69501_RAW.tar 15.6 Mb (http)(custom) TAR (of CEL)
Processed data included within Sample table

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