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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

Adult stem cell plasticity: Fact or artifact?

TL;DR: There has been unprecedented recent interest in stem cells, mainly because of the hope they offer for cell therapy, and examples of plasticity where differentiated cells or their precursors can be reprogrammed by extracellular cues to alter their character in ways that could have important implications for cell Therapy and other forms of regenerative treatment.
Journal ArticleDOI

Nuclear Transplantation, Embryonic Stem Cells, and the Potential for Cell Therapy

TL;DR: The feasibility ofnuclear transfer with gene and cell therapy to treat the immune deficiency of Rag2 mutant mice is demonstrated, thus establishing a paradigm for 'therapeutic cloning' and the potential use of nuclear transfer to study the role of reversible genomic (epigenetic) modifications during tumorigenesis is discussed.
Journal ArticleDOI

Mitotic catastrophe constitutes a special case of apoptosis whose suppression entails aneuploidy

TL;DR: A molecular pathway through which DNA damage, failure to arrest the cell cycle and inhibition of apoptosis can favor the occurrence of cytogenetic abnormalities that are likely to participate in oncogenesis is delineated.
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Cryopreservation of Human Stem Cells for Clinical Application: A Review

TL;DR: The current state of cryopreservation as it pertains to stem cells and in particular the embryonic and iPS cell is reviewed.
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.
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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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