Browse
Submit Data
Databases
API
Help

Dataset Information

0 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

MicroRNA profiling in Mesenchymal Stromal Cells: the tissue source as the missing piece in the puzzle of ageing

ABSTRACT: We compare miRNA profiling in two cell populations of mesenchymal stromal cells focusing on senescence-related changes: Human Dental Pulp Stromal Cells (hDPSCs) and human Periosteum-Derived Progenitor Cells (hPDPCs). After these cells were harvested, total RNA extraction and whole genome miRNA profiling was performed, and DIANA-miRPath analysis was applied to find the target/pathways. Our finding is consistent with the idea that the embryological origin influences cell behavior and the ageing process. Moreover, the two populations activate different downstream mechanisms. Our study strengthens the hypothesis that ageing is driven by numerous mediators interacting through an intricate molecular network, which affects adult stem cells self-renewal capability.

ORGANISM(S): Homo sapiens

PROVIDER: GSE161688 | GEO | 2020/11/18

REPOSITORIES: GEO

ACCESS DATA

Json Xml

Dataset's files

Source:

			Action	DRS
		Other

Items per page:

1 - 1 of 1

Similar Datasets

Expression of mRNA from lung tissue from Systemic Sclerosis patients with interstitial lung disease (SSc-ILD) and healthy controls (HC)

Project description:Objective: MicroRNAs (miRNAs) control key elements of mRNA stability and likely contribute to the dysregulated lung gene expression observed in systemic sclerosis associated interstitial lung disease (SSc-ILD). We analyzed the miRNA gene expression of tissue and cells from SSc-ILD patients. A chronic lung fibrotic murine model was used. Methods: RNA was isolated from lung tissue of 12 SSc-ILD patients and 5 control lungs. High-resolution computed tomography (HRCT) was performed at baseline and 2-3 years after treatment. Lung fibroblasts and PBMCs were isolated from healthy controls and SSc-ILD patients. miRNA and mRNA were analyzed by microarray, quantitative polymerase chain reaction, and/or Nanostring; pathway analysis was performed by DIANA-miRPath v2.0 software. Wild-type and miR-155 deficient (miR-155ko) mice were exposed to bleomycin. Results: Lung miRNA microarray data distinguished patients with SSc-ILD from healthy controls with 185 miRNA differentially expressed (q<0.25). DIANA-miRPath revealed 57 KEGGs pathways related to the most dysregulated miRNAs. miR-155 and miR-143 were strongly correlated with progression of the HRCT score. Lung fibroblasts showed only mild expression of miR-155/miR-21 after several stimuli. miR-155 PBMC expression strongly correlated with lung function tests in SSc-ILD. miR-155ko mice developed milder lung fibrosis, survived longer, and showed a weaker lung induction of several genes after bleomycin exposure compared to wild-type mice. Conclusions: miRNAs are dysregulated in lungs and PBMCs of SSc-ILD patients. Based on mRNA-miRNA interaction analysis and pathway tools, miRNAs may play a role in the progression of the disease. Our findings suggest that targeting miR-155 might provide a novel therapeutic strategy for SSc-ILD. Lung biopsies taken from open lung biopsy from SSc-ILD patients (n=15 samples) and from cancer free control patients (n=5) during ressection of the lung tumor.

2016-08-01 | E-GEOD-81292 | biostudies-arrayexpress

Expression of miRNA from lung tissue from Systemic Sclerosis patients with interstitial lung disease (SSc-ILD) and healthy controls.

2016-08-01 | E-GEOD-81293 | biostudies-arrayexpress

Periosteum contains skeletal stem cells with high bone regenerative potential controlled by Periostin

Project description:Bone regeneration relies on the activation of skeletal stem cells (SSCs) that still remain poorly characterized. Here, we show that periosteum contains SSCs with high bone regenerative potential compared to bone marrow stromal cells/skeletal stem cells (BMSCs) in mice. Although periosteal cells (PCs) and BMSCs are derived from a common embryonic mesenchymal lineage, post-natally PCs exhibit greater clonogenicity, growth and differentiation capacity than BMSCs. During bone repair, PCs can efficiently contribute to cartilage and bone, and integrate long-term after transplantation. Molecular profiling uncovers genes encoding Periostin and other extracellular matrix molecules associated with the enhanced response to injury of PCs. Periostin gene deletion impairs PC functions and fracture consolidation. Periostin-deficient periosteum cannot reconstitute a pool of PCs after injury demonstrating the presence of SSCs within periosteum and the requirement of Periostin in maintaining this pool. Overall our results highlight the importance of analyzing periosteum and PCs to understand bone phenotypes.

2018-10-18 | E-MTAB-6417 | biostudies-arrayexpress

Targeting class A GPCRs for hard tissue regeneration [microarray]

Project description:To investigate class A G protein-coupled receptors (GPCR)-targeted drugs in the regulation of osteogenic differentiation, we investigated the effects of drugs using mesenchymal stromal cells. By applying microarray dataset, we idntified the mRNA expressions profiles in hDPSCs.

2023-01-20 | GSE217436 | GEO

Transcriptomic alterations of stromal cells during ageing

Project description:Transcriptomic alterations of stromal cells during ageing

| PRJNA541905 | ENA

Expression of mRNA from lung tissue from Systemic Sclerosis patients with interstitial lung disease (SSc-ILD) and healthy controls (HC)

2016-08-01 | GSE81292 | GEO

Expression of miRNA from lung tissue from Systemic Sclerosis patients with interstitial lung disease (SSc-ILD) and healthy controls.

2016-08-01 | GSE81293 | GEO

MicroRNA profiling in Mesenchymal Stromal Cells: the tissue source as the missing piece in the puzzle of ageing

Project description:MicroRNA profiling in Mesenchymal Stromal Cells: the tissue source as the missing piece in the puzzle of ageing

| PRJNA679082 | ENA

Rejuvenation of Human Stem Cells from Aged Dental Pulp by High Concentration of Serum Culture ex vivo

Project description:Adult stem cells maintain tissue integrity by continuous cellular turnover or serving progenitor cells. Human dental pulp stem cells (hDPSCs) are adult stem cells that can readily be isolated from extracted teeth, then expanded or stored for tissue repair and regeneration. However, stem cells undergo an aging process characterized by a decline in functional abilities, leading eventually to reduced organ function and delays in tissue repair. Like other stem cells, hDPSCs age and go through cellular senescence but little information is available on the mechanisms of aging or the details of the aged hDPSC phenotype. In this study, we investigated the aging phenotypes of human dental pulp and hDPSCs and attempted to rejuvenate them. In this study, hDPSCs were isolated from 23 third molars and primary cultured. Then, Flow cytometey, growth curve, dubling time, colony-forming-unit assay, cell viability after cryopreservation and in serum-free media culture, differntiation capacity for odonto-, adipo- and chondrogenesis, and RNA sequencing were analyzed. As results, the aged tooth maintained its weight of dental pulp however, the frequency of CD90+CD73+ mesenchymal stem cells inside pulp significantly decreased with donor aging. Moreover, each aged hDPSCs showed lower proliferative abilities, poorer survival rates, decreased tri-differentiation potential, and decline in metabolic activities than young hDPSCs. We also found those aged phenotypes could be recovered by cultivating aged hDPSCs in high concentration of fetal bovine serum (FBS) ex vivo and furthermore, the declined metabolic activities were restored by the culture. Here, we suggest a novel method of intervention for rejuvenating hDPSCs and these results have applications in both regenerative medicine and stem cell biology.

2021-01-28 | GSE165627 | GEO

Gene expression profile during odontogenic differentiation was analyzed using a microarray (miRNA).

Project description:The roles of microRNAs (miRNAs) in odontogenic differentiation of human dental pulp stem cells (hDPSCs) remain largely unexplored. In this study, the underlying molecular mechanism of osteogenic differentiation in hDPSCs is investigated using miRNA profifiling.

2019-10-01 | GSE138180 | GEO

OmicsDI is part of the ELIXIR infrastructure

OmicsDI is an Elixir interoperability service. Learn more ›

Tweets

OmicsDI Databases

PRIDE
PeptideAtlas
MassIVE
JPOST Repository
Physiome Model Repository

EGA
EVA
ENA
LINCS
PAXDB
Cell Collective

MetaboLights
Metabolomics Workbench
MetabolomeExpress
GNPS
BioModels
FAIRDOMHub

ArrayExpress
dbGaP
ExpressionAtlas
GEO
NODE

Information

Databases
Help
API
Contact us
Code on GitHub
Terms of use
Submit Data