Post-natal "mesenchymal" stem cells: the assayable skeletal potency.

J Stem Cells Regen Med

Department of Science, University ROMA TRE, Viale Marconi, 446 - 00146 Rome, Italy.

Published: May 2019

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6586765PMC
http://dx.doi.org/10.46582/jsrm.1501004DOI Listing

Publication Analysis

Top Keywords

post-natal "mesenchymal"
4
"mesenchymal" stem
4
stem cells
4
cells assayable
4
assayable skeletal
4
skeletal potency
4
post-natal
1
stem
1
cells
1
assayable
1

Similar Publications

The MiT/TFE family gene fusion proteins, such as , drive both epithelial (eg, translocation renal cell carcinoma, tRCC) and mesenchymal (eg, perivascular epithelioid cell tumor, PEComa) neoplasms with aggressive behavior. However, no prior mouse models for -related tumors exist and the mechanisms of lineage plasticity induced by this fusion remain unclear. Here, we demonstrate that constitutive murine renal expression of human using Ksp Cadherin-Cre as a driver disrupts kidney development leading to early neonatal renal failure and death.

View Article and Find Full Text PDF

Cell Population-resolved Multi-Omics Atlas of the Developing Lung.

Am J Respir Cell Mol Biol

October 2024

Pacific Northwest National Laboratory, Biological Science Division, Richland, Washington, United States;

The lung is a vital organ that undergoes extensive morphological and functional changes during postnatal development. To disambiguate how different cell populations contribute to organ development, we performed proteomic and transcriptomic analyses of four sorted cell populations from the lung of human subjects aged 0 to 8 years-old with a focus on early life. The cell populations analyzed included epithelial, endothelial, mesenchymal, and immune cells.

View Article and Find Full Text PDF

Characterization and angiogenic potential of CD146 endometrial stem cells.

Stem Cell Res Ther

September 2024

Department of Stem Cells & Regenerative Medicine, D.Y. Patil Education Society (Deemed to be University), D. Y. Patil Vidyanagar, Kasab Bawada, Kolhapur, 416006, Maharashtra, India.

Article Synopsis
  • - The study investigates the role of endometrial stem cells (eSCs) in tissue regeneration and angiogenesis, particularly focusing on CD146 as a key marker that enhances the regenerative and vascular growth potential of these cells.
  • - Researchers isolated eSCs from biopsies of active reproducing women and conducted various analyses to assess their properties, including growth factor secretion and angiogenic capabilities, using functional assays.
  • - The findings potentially pave the way for innovative eSC-based therapies in regenerative medicine and the treatment of vascular disorders by understanding CD146's influence on eSCs' angiogenic functions.
View Article and Find Full Text PDF

Background: Spinal Muscular Atrophy (SMA) is an autosomal-recessive neuromuscular disease affecting children. It is caused by the mutation or deletion of the survival motor neuron 1 (SMN1) gene resulting in lower motor neuron (MN) degeneration followed by motor impairment, progressive skeletal muscle paralysis and respiratory failure. In addition to the already existing therapies, a possible combinatorial strategy could be represented by the use of adipose-derived mesenchymal stem cells (ASCs) that can be obtained easily and in large amounts from adipose tissue.

View Article and Find Full Text PDF

Axin2-CreERT2 mediated knockout of bone morphogenetic protein receptor type 1A caused abnormal secondary dentine and altered cell fate of Axin2-expressing odontogenic cells.

Int Endod J

August 2023

State Key Laboratory of Oral Diseases, National Clinical Research Center for Oral Diseases, Department of Periodontics, West China Hospital of Stomatology, Med-X Center for Materials, Sichuan University, Chengdu, China.

Aim: Inducing odontogenic differentiation and tubular dentine formation is extremely important in dentine repair and tooth regeneration. Bone morphogenic proteins (BMPs) signalling plays a critical role in dentine development and tertiary dentine formation, whilst how BMPR1A-mediated signalling affects odontoblastic differentiation of Axin2-expressing (Axin2 ) odontogenic cells and tubular dentine formation remains largely unknown. This study aims to reveal the cellular and molecular mechanisms involved in the formation of secondary dentine.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!