Literature DB >> 29803144

Induction of quiescence (G0) in bone marrow stromal stem cells enhances their stem cell characteristics.

Mohammad Rumman1, Abhijit Majumder2, Linda Harkness3, Balu Venugopal4, M B Vinay4, Malini S Pillai4, Moustapha Kassem5, Jyotsna Dhawan6.   

Abstract

Several studies have suggested that bone marrow stromal steam cells (BMSC) exist in a quiescent state (G0) within the in vivo niche; however, an explicit analysis of the biology of G0 state-BMSC has not been reported. We hypothesized that induction of G0 in BMSC might enhance their stem cell properties. Thus, we induced quiescence in BMSC in vitro by (a) suspension culture in a viscous medium or (b) culture on soft polyacrylamide substrate; and examined their molecular and functional phenotype. Induction of G0 was confirmed by bromo-deoxyuridine (BrdU) labelling and analysis of cell cycle gene expression. Upon reactivation and re-entry into cell cycle, G0 state-BMSC exhibited enhanced clonogenic self-renewal, preferential differentiation into osteoblastic rather than adipocytic cells and increased ectopic bone formation when implanted subcutaneously in vivo in immune-deficient mice, compared to asynchronous proliferating (pre-G0) BMSC. Global gene expression profiling revealed reprogramming of the transcriptome during G0 state including significant alterations in relevant pathways and expression of secreted factors, suggesting altered autocrine and paracrine signaling by G0 state-BMSC and a possible mechanism for enhanced bone formation. G0 state-BMSC might provide a clinically relevant model for understanding the in vivo biology of BMSC.
Copyright © 2018. Published by Elsevier B.V.

Entities:  

Keywords:  Adhesion; BMSC; Cell cycle; Osteoblastic differentiation; Quiescence (G0); Reprogramming; Substrate stiffness; Suspension culture; Transcriptome

Mesh:

Year:  2018        PMID: 29803144     DOI: 10.1016/j.scr.2018.05.010

Source DB:  PubMed          Journal:  Stem Cell Res        ISSN: 1873-5061            Impact factor:   2.020


  10 in total

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Journal:  J Mater Sci Mater Med       Date:  2021-08-18       Impact factor: 3.896

2.  The Plasticity of Mesenchymal Stem Cells in Regulating Surface HLA-I.

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3.  Autophagy mediates serum starvation-induced quiescence in nucleus pulposus stem cells by the regulation of P27.

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4.  Soft substrate maintains proliferative and adipogenic differentiation potential of human mesenchymal stem cells on long-term expansion by delaying senescence.

Authors:  Sanjay Kumar Kureel; Pankaj Mogha; Akshada Khadpekar; Vardhman Kumar; Rohit Joshi; Siddhartha Das; Jayesh Bellare; Abhijit Majumder
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5.  Transforming Growth Factor β-Activated Kinase 1 Regulates Mesenchymal Stem Cell Proliferation Through Stabilization of Yap1/Taz Proteins.

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Journal:  Stem Cells       Date:  2019-11-18       Impact factor: 6.277

6.  New strategy of bone marrow mesenchymal stem cells against oxidative stress injury via Nrf2 pathway: oxidative stress preconditioning.

Authors:  Fei Zhang; Wuxun Peng; Jian Zhang; Wentao Dong; Dajiang Yuan; Yinggang Zheng; Zhenwen Wang
Journal:  J Cell Biochem       Date:  2019-07-26       Impact factor: 4.429

7.  A novel in vitro 3D model of the human bone marrow to bridge the gap between in vitro and in vivo genotoxicity testing.

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Journal:  Mutagenesis       Date:  2022-05-04       Impact factor: 2.954

8.  Novel Mesenchymal Stem Cell Spheroids with Enhanced Stem Cell Characteristics and Bone Regeneration Ability.

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Journal:  Stem Cells Transl Med       Date:  2022-04-29       Impact factor: 7.655

9.  The primary cilium dampens proliferative signaling and represses a G2/M transcriptional network in quiescent myoblasts.

Authors:  Nisha Venugopal; Ananga Ghosh; Hardik Gala; Ajoy Aloysius; Neha Vyas; Jyotsna Dhawan
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Review 10.  The Role of Extracellular Vesicles in the Development of a Cancer Stem Cell Microenvironment Niche and Potential Therapeutic Targets: A Systematic Review.

Authors:  Thomas J Brown; Victoria James
Journal:  Cancers (Basel)       Date:  2021-05-18       Impact factor: 6.639

  10 in total

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