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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

Cell-fusion-mediated somatic-cell reprogramming: a mechanism for tissue regeneration.

TL;DR: This work has shown that injury to a tissue can enhance spontaneous cell–cell fusion events, and if this process is deregulated, this would provide a mechanism for cancer development.
Journal ArticleDOI

Nanopatterned bulk metallic glass-based biomaterials modulate macrophage polarization.

TL;DR: This study demonstrates that nanopatterning of BMG implants is a promising technique to selectively polarize macrophages to modulate the immune response, and also presents an effective tool to study mechanisms of macrophage polarization and function.
Journal ArticleDOI

The role of circulating precursors in vascular repair and lesion formation.

TL;DR: Recent findings on circulating vascular progenitor cells are overviews and potential therapeutic strategies that target these cells to treat occlusive vascular diseases are described.
Journal ArticleDOI

Fusion of Human Hematopoietic Progenitor Cells and Murine Cardiomyocytes Is Mediated by α4β1 Integrin/Vascular Cell Adhesion Molecule-1 Interaction

TL;DR: It is shown that hypoxia and cytokines increase fusion of human peripheral blood CD34-positive cells and murine cardiomyocytes in vitro by up to 7-fold, and this is blocked by anti-&agr;4&bgr;1 or anti-vascular cell adhesion molecule (VCAM)-1, leading to cell cycle reentry and cellular proliferation.
Book ChapterDOI

Retinoids in lung development and regeneration.

TL;DR: Recent data from animal studies suggest that retinoids can induce regeneration of alveoli in young adults, which, if relevant to humans, might be the first potential treatment for diseases such as emphysema or bronchopulmonary dysplasia.
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.
Journal ArticleDOI

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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