Cell‐to‐cell cross‐talk between mesenchymal stem cells and cardiomyocytes in co‐culture

The goals of the study were: (1) to explore the communication between human mesenchymal stem cells (MSC) and rat cardiac myocytes resulting in differentiation of the stem cells and, (2) to evaluate the role of mitochondria in it. Light and fluorescence microscopy as well as scanning electron microsc...

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Published inJournal of cellular and molecular medicine Vol. 12; no. 5a; pp. 1622 - 1631
Main Authors Plotnikov, E. Y., Khryapenkova, T. G., Vasileva, A. K., Marey, M. V., Galkina, S. I., Isaev, N. K., Sheval, E. V., Polyakov, V. Y., Sukhikh, G. T., Zorov, D. B.
Format Journal Article
LanguageEnglish
Published Oxford, UK Blackwell Publishing Ltd 01.09.2008
John Wiley & Sons, Inc
Subjects
Animals
Bone marrow
cardiomyocyte
Cardiomyocytes
Cell Communication
Cell culture
Cell differentiation
Cell interactions
cell therapy
Coculture Techniques
Cytoplasm - metabolism
Fluorescence microscopy
foetal stem cells
Heart
Humans
Medical research
Mesenchymal stem cells
Mesenchymal Stromal Cells - cytology
Mesenchymal Stromal Cells - metabolism
Microscopy
Microscopy, Electron
Mitochondria
Myocardium
Myocytes
Myocytes, Cardiac - cytology
Myocytes, Cardiac - metabolism
Myosin
Myosins - metabolism
Nanotubes
Rats
Rodents
Scanning electron microscopy
Stem cell transplantation
Stem cells
Studies
Transmission electron microscopy
tunnelling nanotubes
United States > US
Online AccessGet full text
ISSN1582-1838
1582-4934
DOI10.1111/j.1582-4934.2007.00205.x

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Abstract The goals of the study were: (1) to explore the communication between human mesenchymal stem cells (MSC) and rat cardiac myocytes resulting in differentiation of the stem cells and, (2) to evaluate the role of mitochondria in it. Light and fluorescence microscopy as well as scanning electron microscopy revealed that after co‐cultivation, cells formed intercellular contacts and transient exchange with cytosolic elements could be observed. The transport of cytosolic entity had no specific direction. Noticeably, mitochondria also could be transferred to the recipient cells in a unidirectional fashion (towards cardiomyocytes only). Transmission electron microscopy revealed significant variability in both the diameter of intercellular contacting tubes and their shape. Inside of these nanotubes mitochondria‐resembling structures were identified. Moreover, after co‐cultivation with cardiomyocytes, expression of human‐specific myosin was revealed in MSC. Thus, we speculate that: (1) transport of intracellular elements to MSC possibly can determine the direction of their differentiation and, (2) mitochondria may be involved in the mechanism of the stem cell differentiation. It looks plausible that mitochondrial transfer to recipient cardiomyocytes may be involved in the mechanism of failed myocardium repair after stem cells transplantation.
AbstractList The goals of the study were: (1) to explore the communication between human mesenchymal stem cells (MSC) and rat cardiac myocytes resulting in differentiation of the stem cells and, (2) to evaluate the role of mitochondria in it. Light and fluorescence microscopy as well as scanning electron microscopy revealed that after co-cultivation, cells formed intercellular contacts and transient exchange with cytosolic elements could be observed. The transport of cytosolic entity had no specific direction. Noticeably, mitochondria also could be transferred to the recipient cells in a unidirectional fashion (towards cardiomyocytes only). Transmission electron microscopy revealed significant variability in both the diameter of intercellular contacting tubes and their shape. Inside of these nanotubes mitochondria-resembling structures were identified. Moreover, after co-cultivation with cardiomyocytes, expression of human-specific myosin was revealed in MSC. Thus, we speculate that: (1) transport of intracellular elements to MSC possibly can determine the direction of their differentiation and, (2) mitochondria may be involved in the mechanism of the stem cell differentiation. It looks plausible that mitochondrial transfer to recipient cardiomyocytes may be involved in the mechanism of failed myocardium repair after stem cells transplantation.
The goals of the study were: (1) to explore the communication between human mesenchymal stem cells (MSC) and rat cardiac myocytes resulting in differentiation of the stem cells and, (2) to evaluate the role of mitochondria in it. Light and fluorescence microscopy as well as scanning electron microscopy revealed that after co-cultivation, cells formed intercellular contacts and transient exchange with cytosolic elements could be observed. The transport of cytosolic entity had no specific direction. Noticeably, mitochondria also could be transferred to the recipient cells in a unidirectional fashion (towards cardiomyocytes only). Transmission electron microscopy revealed significant variability in both the diameter of intercellular contacting tubes and their shape. Inside of these nanotubes mitochondria-resembling structures were identified. Moreover, after co-cultivation with cardiomyocytes, expression of human-specific myosin was revealed in MSC. Thus, we speculate that: (1) transport of intracellular elements to MSC possibly can determine the direction of their differentiation and, (2) mitochondria may be involved in the mechanism of the stem cell differentiation. It looks plausible that mitochondrial transfer to recipient cardiomyocytes may be involved in the mechanism of failed myocardium repair after stem cells transplantation. [PUBLICATION ABSTRACT]
The goals of the study were: (1) to explore the communication between human mesenchymal stem cells (MSC) and rat cardiac myocytes resulting in differentiation of the stem cells and, (2) to evaluate the role of mitochondria in it. Light and fluorescence microscopy as well as scanning electron microscopy revealed that after co-cultivation, cells formed intercellular contacts and transient exchange with cytosolic elements could be observed. The transport of cytosolic entity had no specific direction. Noticeably, mitochondria also could be transferred to the recipient cells in a unidirectional fashion (towards cardiomyocytes only). Transmission electron microscopy revealed significant variability in both the diameter of intercellular contacting tubes and their shape. Inside of these nanotubes mitochondria-resembling structures were identified. Moreover, after co-cultivation with cardiomyocytes, expression of human-specific myosin was revealed in MSC. Thus, we speculate that: (1) transport of intracellular elements to MSC possibly can determine the direction of their differentiation and, (2) mitochondria may be involved in the mechanism of the stem cell differentiation. It looks plausible that mitochondrial transfer to recipient cardiomyocytes may be involved in the mechanism of failed myocardium repair after stem cells transplantation.The goals of the study were: (1) to explore the communication between human mesenchymal stem cells (MSC) and rat cardiac myocytes resulting in differentiation of the stem cells and, (2) to evaluate the role of mitochondria in it. Light and fluorescence microscopy as well as scanning electron microscopy revealed that after co-cultivation, cells formed intercellular contacts and transient exchange with cytosolic elements could be observed. The transport of cytosolic entity had no specific direction. Noticeably, mitochondria also could be transferred to the recipient cells in a unidirectional fashion (towards cardiomyocytes only). Transmission electron microscopy revealed significant variability in both the diameter of intercellular contacting tubes and their shape. Inside of these nanotubes mitochondria-resembling structures were identified. Moreover, after co-cultivation with cardiomyocytes, expression of human-specific myosin was revealed in MSC. Thus, we speculate that: (1) transport of intracellular elements to MSC possibly can determine the direction of their differentiation and, (2) mitochondria may be involved in the mechanism of the stem cell differentiation. It looks plausible that mitochondrial transfer to recipient cardiomyocytes may be involved in the mechanism of failed myocardium repair after stem cells transplantation.
Author Zorov, D. B.
Polyakov, V. Y.
Isaev, N. K.
Plotnikov, E. Y.
Marey, M. V.
Sukhikh, G. T.
Khryapenkova, T. G.
Sheval, E. V.
Vasileva, A. K.
Galkina, S. I.
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/18088382$$D View this record in MEDLINE/PubMed
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ContentType Journal Article
Copyright 2008 The Authors Journal compilation © 2008 Foundation for Cellular and Molecular Medicine/Blackwell Publishing Ltd
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2008. This work is published under https://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
2008 The Authors Journal compilation © 2008 Foundation for Cellular and Molecular Medicine/Blackwell Publishing Ltd 2008
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Snippet The goals of the study were: (1) to explore the communication between human mesenchymal stem cells (MSC) and rat cardiac myocytes resulting in differentiation...
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SourceType Open Access Repository
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Enrichment Source
Publisher
StartPage 1622
SubjectTerms Animals
Bone marrow
cardiomyocyte
Cardiomyocytes
Cell Communication
Cell culture
Cell differentiation
Cell interactions
cell therapy
Coculture Techniques
Cytoplasm - metabolism
Fluorescence microscopy
foetal stem cells
Heart
Humans
Medical research
Mesenchymal stem cells
Mesenchymal Stromal Cells - cytology
Mesenchymal Stromal Cells - metabolism
Microscopy
Microscopy, Electron
Mitochondria
Myocardium
Myocytes
Myocytes, Cardiac - cytology
Myocytes, Cardiac - metabolism
Myosin
Myosins - metabolism
Nanotubes
Rats
Rodents
Scanning electron microscopy
Stem cell transplantation
Stem cells
Studies
Transmission electron microscopy
tunnelling nanotubes
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Title Cell‐to‐cell cross‐talk between mesenchymal stem cells and cardiomyocytes in co‐culture
URI https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fj.1582-4934.2007.00205.x
https://www.ncbi.nlm.nih.gov/pubmed/18088382
https://www.proquest.com/docview/217185212
https://www.proquest.com/docview/3074744575
https://www.proquest.com/docview/69792980
https://pubmed.ncbi.nlm.nih.gov/PMC3918078
Volume 12
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