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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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Journal ArticleDOI

Facultative stem cells in liver and pancreas: fact and fancy.

TL;DR: The evidence for FSCs in two mammalian organs, the liver and the pancreas, are reviewed, and alternative models that could account for regeneration in these organs are discussed.
Journal ArticleDOI

Bone morphogenetic protein-2 induces differentiation of multipotent C3H10T1/2 cells into osteoblasts, chondrocytes, and adipocytes in vivo and in vitro

TL;DR: Bone morphogenetic protein (BMP-2) can induce the differentiation of C3H10T1/2 into osteoblasts, chondrocytes, and adipocytes in both in vivo and in vitro conditions, and that C3 H10T 1/2 could be used to examine the B MP-2-induced regulatory mechanisms of mesenchymal differentiation.
Journal ArticleDOI

Stem cells for liver tissue repair: Current knowledge and perspectives

TL;DR: The present review focuses on the current knowledge of the stem cell potential for liver therapy, discussion of the characteristics of the principal cell candidates and the methods to demonstrate their hepatic potential in vitro and in vivo, and the future clinical applications of stem cells for liver tissue repair.
Journal Article

Comparison of proliferative and multilineage differentiation potential of sheep mesenchymal stem cells derived from bone marrow, liver, and adipose tissue.

TL;DR: All three sources of fetal sheep MSCs had the identical trilineage differentiation potential and the proliferative capacity of liver and bone marrow derived M SCs were similar at different cell seeding densities except for the higher fold increase in B-MSCs at 2700 cells/cm 2 density.
Journal ArticleDOI

Current perspectives in mesenchymal stem cell therapies for osteoarthritis.

TL;DR: The history and early uses of MSCs in cartilage regeneration are reviewed, different approaches in current trends are explained and evaluated, and the focus has completely shifted towards direct intra-articular injections into affected joints.
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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