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Journal ArticleDOI

Bone marrow as a potential source of hepatic oval cells.

TLDR
A stem cell associated with the bone marrow has epithelial cell lineage capability and a proportion of the regenerated hepatic cells were shown to be donor-derived.
Abstract
Bone marrow stem cells develop into hematopoietic and mesenchymal lineages but have not been known to participate in production of hepatocytes, biliary cells, or oval cells during liver regeneration. Cross-sex or cross-strain bone marrow and whole liver transplantation were used to trace the origin of the repopulating liver cells. Transplanted rats were treated with 2-acetylaminofluorene, to block hepatocyte proliferation, and then hepatic injury, to induce oval cell proliferation. Markers for Y chromosome, dipeptidyl peptidase IV enzyme, and L21-6 antigen were used to identify liver cells of bone marrow origin. From these cells, a proportion of the regenerated hepatic cells were shown to be donor-derived. Thus, a stem cell associated with the bone marrow has epithelial cell lineage capability.

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Citations
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Journal ArticleDOI

Reproducible methodology for the isolation of mesenchymal stem cells from human umbilical cord and its potential for cardiomyocyte generation.

TL;DR: Extensive phenotypic characterization analysis of these cells, using flow cytometry and antibody staining methods, have shown that they were able to isolate a pure population of the mesenchymal lineage cells that is devoid of haematopoietic and endothelial cell contaminants.
Journal ArticleDOI

The migration of bone marrow-derived non-hematopoietic tissue-committed stem cells is regulated in an SDF-1-, HGF-, and LIF-dependent manner.

TL;DR: These findings further support the theory of the BM as a “hideout” for TCSCs and suggest that their presence in BM tissue should be considered before experimental evidence is interpreted simply as transdifferentiation/plasticity of hematopoietic stem cells.
Journal ArticleDOI

Somatic stem cell plasticity: current evidence and emerging concepts.

TL;DR: A review of the current evidence for stem cell plasticity can be found in this article, where a broadening developmental potential of bone marrow-derived stem cells leading to the differentiation capacities of stem cells from nonhematopoietic tissues is discussed.
Journal ArticleDOI

The vagal nerve stimulates activation of the hepatic progenitor cell compartment via muscarinic acetylcholine receptor type 3

TL;DR: The hepatic vagus branch stimulates activation of the hepatic progenitor cell compartment in diseased liver, most likely through binding of acetylcholine to the M3 receptor expressed on these cells.
Journal ArticleDOI

The biology of hematopoietic stem cells.

TL;DR: This review focuses exclusively on the biology of hematopoietic stem cells (HSCs) and their immediate progeny, and many of the concepts established can be considered fundamental tenets of an evolving stem cell paradigm applicable to many regenerating cellular systems.
References
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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 Article

In vivo differentiation of rat liver oval cells into hepatocytes.

TL;DR: The data indicate that oval cells can differentiate to hepatocytes and may have an important physiological function as a source of major serum proteins when hepatocytes are unable to synthesize these proteins.
Journal ArticleDOI

Presence of hematopoietic stem cells in the adult liver

TL;DR: The data obtained from the mouse study strongly suggest that hematopoietic stem cells residing in the donor liver are responsible for mixed chimerism and maintenance of tolerance after liver transplantation.
Journal Article

Expression of stem cell factor and its receptor, c-kit, during liver regeneration from putative stem cells in adult rat.

TL;DR: The SCF/c-kit system may, possibly in combination with other growth factor/receptor systems, be involved in the early activation of the hepatic stem cells as well as in the expansion and differentiation of oval cells.
Journal ArticleDOI

Variable chimerism, graft-versus-host disease, and tolerance after different kinds of cell and whole organ transplantation from Lewis to brown Norway rats.

TL;DR: Both the GVHD propensity and tolerogenicity in these experiments were closely associated with recipient tissue chimerism 30 and 100 days after the experiments began, and these observations provide guidelines that should be considered in devising leukocyte augmentation protocols for human whole organ recipients.
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