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Journal ArticleDOI

Formation of bone and cartilage by marrow stromal cells in diffusion chambers in vivo.

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TLDR
The present results suggest that postnatal marrow contains osteogenic precursors with the potential to differentiate via either of the two major paths followed during skeletal development in the embryo.
Abstract
When freshly isolated rabbit marrow cells were cultured either in vitro or in diffusion chambers in vivo, the hemopoietic cells disappeared and there was a proliferation of the stromal cell population. The colonies formed in vitro were mainly fibroblastic, and this cell type predominated in confluent cultures. Staining for alkaline phosphatase activity and for the Von Kossa reaction was negative in in vitro cultures. However, marrow cell suspensions or fibroblasts harvested from in vitro culture of marrow cells, gave rise to a mixture of bone, cartilage and fibrous tissue in diffusion chambers implanted into the peritoneal cavity. In contrast, only a soft fibrous tissue developed from spleen fibroblasts in diffusion chambers. Differentiation of osteogenic tissue within diffusion chambers fell into two categories: (1) Formation of bone in a fibrous layer surrounding cartilage; (2) intramembranous bone formed directly within fibrous tissue unassociated with cartilage. In both cases alkaline phosphatase activity appeared before the onset of mineralization, and decreased as the first signs of mineral became apparent. The present results suggest that postnatal marrow contains osteogenic precursors with the potential to differentiate via either of the two major paths followed during skeletal development in the embryo. Clonal analysis of the marrow stromal cell population will be required to clarify whether osteo-, chondro-, and fibrogenic cells are the products of one stromal cell line modulated by the microenvironment, or whether there are distinct cell lines for each type.

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Journal ArticleDOI

In vitro chondrogenesis of bone marrow-derived mesenchymal progenitor cells

TL;DR: A culture system that facilitates the chondrogenic differentiation of rabbit bone marrow-derived mesenchymal progenitor cells has been developed in this article, where cells obtained in bone marrow aspirates were first isolated by monolayer culture and then transferred into tubes and allowed to form three-dimensional aggregates in a chemically defined medium.
Journal ArticleDOI

Concise review: mesenchymal stem cells: their phenotype, differentiation capacity, immunological features, and potential for homing.

TL;DR: Harnessing the migratory potential of MSCs by modulating their chemokine‐chemokine receptor interactions may be a powerful way to increase their ability to correct inherited disorders of mesenchymal tissues or facilitate tissue repair in vivo.
Journal ArticleDOI

Osteogenic differentiation of purified, culture‐expanded human mesenchymal stem cells in vitro

TL;DR: In this paper, a reproducible system for the in vitro osteogenic differentiation of human mesenchymal stem cells (MSCs) was presented. But the authors did not consider the effect of changes in the microenvironment upon the process.
Journal ArticleDOI

Cardiomyocytes can be generated from marrow stromal cells in vitro

TL;DR: Analysis of the isoform of contractile protein genes, such as myosin heavy chain, myos in light chain, and alpha-actin, indicated that their muscle phenotype was similar to that of fetal ventricular cardiomyocytes.
Journal ArticleDOI

Bone Marrow Stromal Stem Cells: Nature, Biology, and Potential Applications

TL;DR: Bone marrow stromal cells are progenitors of skeletal tissue components such as bone, cartilage, the hematopoiesis‐supporting stroma, and adipocytes and represent an important paradigm of post‐natal nonhematopoietic stem cells, and an easy source for potential therapeutic use.
References
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Journal ArticleDOI

THE USE OF LEAD CITRATE AT HIGH pH AS AN ELECTRON-OPAQUE STAIN IN ELECTRON MICROSCOPY

TL;DR: The stain reported here differs from previous alkaline lead stains in that the chelating agent, citrate, is in sufficient excess to sequester all lead present, and is less likely to contaminate sections.
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The development of fibroblast colonies in monolayer cultures of guinea-pig bone marrow and spleen cells.

TL;DR: The linear increase in the number of colonies with increasing numbers of explanted cells and the distribution of male and female cells in mixed cultures support the view that fibroblast colonies are clones.
Journal ArticleDOI

Stromal cells responsible for transferring the microenvironment of the hemopoietic tissues. Cloning in vitro and retransplantation in vivo.

TL;DR: It is concluded that stromal precursors are the cells responsible for the transfer of the microenvironmont typical of the given homopoiotic tissue.
Journal ArticleDOI

The histogenesis of cartilage and bone in the long bones of the embryonic fowl

TL;DR: The development and cytology of cartilage and bone in the limbs from the fifty‐second hour of incubation to the first day after hatching are described.
Journal ArticleDOI

The hematopoietic microenvironment of the bone marrow: An ultrastructural study of the stroma in rats

TL;DR: The stroma and vascular sinuses are described by scanning and transmission electron microscopy and in freeze‐fracture etch replicas in normal rat femoral marrow and in rats made eosinophilic by larvae of trichinella spiralis.
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