Rat Bone Marrow Mesenchymal Stem Cells

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Cat.No.
CSC-C4191X
Description
Rat Bone Marrow Mesenchymal Stem Cells are derived from the tibias and femurs of 1-week old Sprague Dawley Rats. Rat Bone Marrow Mesenchymal Stem Cells are grown in T25 tissue culture flasks pre-coated with gelatin-based solution for 0.5 hour and incubated in Creative Bioarray's Cell Culture Medium for 7-15 days. Cultures are then expanded. Prior to shipping, cells are detached from flasks and immediately cryo-preserved in vials. Each vial contains at least 1x10^6 cells per ml and is delivered frozen.
Rat Bone Marrow Mesenchymal StemCells are negative for bacteria, yeast, fungi, and mycoplasma. Cells can be expanded on a multiwell culture plate ready for experiments under the cell culture conditions specified by Creative Bioarray. Repeated freezing and thawing of cells is not recommended.
Mouse Bone Marrow Mesenchymal Stem Cells are tested for expression of markers using antibodies, CD44, Sca-1 and CD29 by flow cytometry.
Standard biochemical procedures performed include the assays of cell to cell interaction, PCR, Western blotting, immunoprecipitation, immunofluorescent staining, immunofluorescent flow cytometry or generating cell derivatives for desired research applications.
Species
Rat
Storage and Shipping
Creative Bioarray will ship frozen cells on dry ice. On receipt, immediately transfer frozen cells to liquid nitrogen (-180 ℃) until ready for experimental use. Live-cell shipment is also available on request.
Citation Guidance
If you use this products in your scientific publication, it should be cited in the publication as: Creative Bioarray cat no. If your paper has been published, please click here to submit the PubMed ID of your paper to get a coupon.

Rat Bone Marrow Mesenchymal Stem Cells (BM-MSCs), also termed bone marrow-derived mesenchymal stromal cells, are nonhematopoietic stromal populations isolated from rat bone marrow. Under appropriate culture conditions, they exhibit plastic adherence, fibroblast-like morphology, and the capacity for osteogenic, adipogenic, and chondrogenic differentiation. These characteristics make them a versatile model for investigating mesenchymal lineage commitment, stromal biology, and mechanisms relevant to tissue regeneration.

A principal advantage is their capacity for culture expansion, enabling sufficient cell numbers for complementary molecular and functional experiments. Their differentiation potential supports controlled studies of extracellular matrix production, mineralization, lipid accumulation, and cartilage-associated matrix formation.

Beyond differentiation, these cells provide a platform for investigating paracrine signaling and immunomodulatory interactions. Rat BM-MSCs secrete bioactive factors whose abundance and activity can change with environmental stimulation. Conditioned-medium studies have demonstrated effects on neurite outgrowth and vascular smooth muscle cell behavior, supporting investigation of mechanisms that do not require direct differentiation into replacement tissue. This functional flexibility enables studies of cellular communication, preconditioning strategies, and factors contributing to repair responses.

Their compatibility with established rat experimental models further facilitates comparisons between in vitro findings and tissue-level outcomes. Applications include biomaterial evaluation, bone regeneration research, and analysis of immune–stromal interactions.

Twofold Effects of Zn2+ on Bone Marrow Mesenchymal Stem Cells—Osteogenesis or Apoptosis

Zinc (Zn) is a bioabsorbable metal that shows great potential as an implant material for orthopedic applications. Suitable concentrations of zinc ions promote osteogenesis, while excess zinc ions cause apoptosis. As a result, the conflicting impacts of Zn2+ concentration on osteogenesis could prove to be significant problems for the creation of novel materials.

This study thoroughly examined the cell viability, proliferation, and osteogenic differentiation of rat bone marrow mesenchymal stem cells (rBMSCs) cultured in various concentrations of Zn2+ in vitro. The effective promotion of cell survival, proliferation, migration, and osteogenic differentiation of bone marrow mesenchymal stem cell (BMSCs) may be achieved at a low concentration of Zn2+ (125 μM). The excessively high concentration of zinc ions (>250 μM) not only reduces BMSCs’ viability and proliferation but also causes them to suffer apoptosis due to the disturbed zinc homeostasis and excessive Zn2+. Moreover, transcriptome sequencing was used to examine the underlying mechanisms of zinc-induced osteogenic differentiation with particular attention paid to the PI3K-AKT and TGF-β pathways. The present investigation elucidated the dual impacts of Zn2+ microenvironments on the osteogenic characteristics of rBMSCs and might offer significant insights for refining the blueprint for zinc-based biomaterials.

Effect of zinc ions on osteogenic differentiation of rBMSCs in vitro.
Fig. 1. Effect of zinc ions on osteogenic differentiation of rBMSCs in vitro (Liu, Yu, et al., 2024).

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