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Journal ArticleDOI

Bone marrow cells adopt the phenotype of other cells by spontaneous cell fusion

TLDR
It is demonstrated that mouse bone marrow cells can fuse spontaneously with embryonic stem cells in culture in vitro that contains interleukin-3, which, without detailed genetic analysis, might be interpreted as ‘dedifferentiation’ or transdifferentiation.
Abstract
Recent studies have demonstrated that transplanted bone marrow cells can turn into unexpected lineages including myocytes, hepatocytes, neurons and many others. A potential problem, however, is that reports discussing such 'transdifferentiation' in vivo tend to conclude donor origin of transdifferentiated cells on the basis of the existence of donor-specific genes such as Y-chromosome markers. Here we demonstrate that mouse bone marrow cells can fuse spontaneously with embryonic stem cells in culture in vitro that contains interleukin-3. Moreover, spontaneously fused bone marrow cells can subsequently adopt the phenotype of the recipient cells, which, without detailed genetic analysis, might be interpreted as 'dedifferentiation' or transdifferentiation.

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Journal ArticleDOI

Epigenetic reprogramming of nuclei using cell extracts.

TL;DR: This review highlights recent observations leading to the concept that extracts derived from pluripotent cells contain regulatory components capable of reprogramming somatic nuclear function.
Journal ArticleDOI

Liver biopsies from human females contain male hepatocytes in the absence of transplantation.

TL;DR: Male cells found in livers of women with sons include cells that express hepatocyte antigens, suggesting that transplantation and stem cell differentiation studies using sex difference to conclude that donor cells regenerate liver may be confounded by fetal microchimerism.
Journal ArticleDOI

Xenotransplantation of Long‐Term‐Cultured Swine Bone Marrow‐Derived Mesenchymal Stem Cells

TL;DR: The capacity to massively expand MSC lines without loss of therapeutic efficacy may prove to be useful in the clinical setting where “off the shelf” MSCs may be required for interventions in patients with acute coronary syndromes.
Journal ArticleDOI

Homing genes, cell therapy and stroke.

TL;DR: Recent studies into how BMSCs reach, recognize, and function in cerebral ischemic tissues, with particular regard to phenotypical reprogramming of stem cells, or "stem cell plasticity", are summarized.
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Bi-directional Exchange of Membrane Components Occurs during Co-culture of Mesenchymal Stem Cells and Nucleus Pulposus Cells.

TL;DR: A range of potential mechanisms for exchange of cellular components or information that may direct changes in intervertebral disc degeneration are investigated, including cell fusion, gap-junctional communication and exchange of membrane components by direct transfer or via microvesicle formation.
References
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Journal ArticleDOI

Multilineage Potential of Adult Human Mesenchymal Stem Cells

TL;DR: Adult stem cells isolated from marrow aspirates of volunteer donors could be induced to differentiate exclusively into the adipocytic, chondrocytic, or osteocytic lineages.
Journal ArticleDOI

Viable offspring derived from fetal and adult mammalian cells

TL;DR: The birth of lambs from differentiated fetal and adult cells confirms that differentiation of that cell did not involve the irreversible modification of genetic material required for development to term and reinforces previous speculation that by inducing donor cells to become quiescent it will be possible to obtain normal development from a wide variety of differentiated cells.
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Formation of Pluripotent Stem Cells in the Mammalian Embryo Depends on the POU Transcription Factor Oct4

TL;DR: It is reported that the activity of Oct4 is essential for the identity of the pluripotential founder cell population in the mammalian embryo and also determines paracrine growth factor signaling from stem cells to the trophectoderm.
Journal ArticleDOI

Muscle Regeneration by Bone Marrow-Derived Myogenic Progenitors

TL;DR: Transplantation of genetically marked bone marrow into immunodeficient mice revealed that marrow-derived cells migrate into areas of induced muscle degeneration, undergo myogenic differentiation, and participate in the regeneration of the damaged fibers.
Journal ArticleDOI

Multi-Organ, Multi-Lineage Engraftment by a Single Bone Marrow-Derived Stem Cell

TL;DR: It is shown that rare cells that home to bone marrow can LTR primary and secondary recipients, and this finding may contribute to clinical treatment of genetic disease or tissue repair.
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