NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Series GSE124119 Query DataSets for GSE124119
Status Public on Dec 25, 2020
Title Distinct types of stem cell divisions determine organ regeneration and aging in hair follicles
Organism Mus musculus
Experiment type Expression profiling by array
Summary Aging organs functionally and structurally decline with the loss of their regenerative capabilities, yet the existence of distinct cell division programs that determine organ fates is unknown. Hair follicles, mammalian mini-organs that grow hair, miniaturize by aging. Here we report that hair follicle regeneration and aging are driven by distinct cell division types of hair follicle stem cells (HFSCs). Cell fate tracing and cell division axis analysis in mice revealed that HFSCs undergo symmetric and asymmetric cell divisions to generate a new bulge, yet preferentially provoke “stress-responsive type” asymmetric cell divisions that generate aberrantly differentiating cells upon age/stress. That dynamic program with repetitive divisions efficiently eradicates those cells through defective association and stabilization of a hemidesmosomal protein COL17A1 and a cell-polarity-protein aPKCλ in HFSCs, thereby causing organ aging. The forced stabilization of COL17A1 rescued organ aging through aPKCλ stabilization. These results demonstrate that distinct cell division programs govern tissue/organ fates.
 
Overall design Hair follicle stem cells (HFSCs) and Interfollicular epidermis (IFE) from young/aged Col17a1, aPKCλ cKO and young/aged COL17A1 transgenic mice were FACS isolated and RNA was extracted before being hybridized Agillent microarray. We obtained a gene of list by comparing Young/Aged, Col17a1/aPKCλ cKO and young/aged COL17A1 transgenic mice.
Web link https://www.nature.com/articles/s43587-021-00033-7
 
Contributor(s) Matsumura H, Nishimura EK
Citation missing Has this study been published? Please login to update or notify GEO.
Submission date Dec 19, 2018
Last update date Mar 28, 2021
Contact name Hiroyuki Matsumura
E-mail(s) matsscm@tmd.ac.jp
Phone +81-3-5803-5838
Organization name Tokyo medical and dental university
Department Medical research institute
Lab Stem cell medicine
Street address 1-5-45, Yushima
City Tokyo
State/province Bunkyo-ku
ZIP/Postal code 113-8510
Country Japan
 
Platforms (1)
GPL10787 Agilent-028005 SurePrint G3 Mouse GE 8x60K Microarray (Probe Name version)
Samples (16)
GSM3521175 Cont_tHFSCs
GSM3521176 Cont_aHFSCs
GSM3521177 Col17a1cKO_tHFSCs
Relations
BioProject PRJNA510803

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
GSE124119_RAW.tar 188.8 Mb (http)(custom) TAR (of TXT)
Processed data included within Sample table

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap