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Mesenchymal stem cells from the jaw bone marrow have significant functions in diverse differentiation, self-renewal, and immune modulation. They have emerged as a crucial reservoir of precursor cells in gene therapy, tissue engineering, and regenerative medicine. Here, we present a unique method for isolating jaw bone marrow mesenchymal stem cells in rats.
Bone marrow mesenchymal stem cells (BMMSCs) are a type of stem cell with multi-directional differentiation potential. Compared with BMMSCs derived from appendicular bones, BMMSCs derived from the jaw have greater proliferative and osteogenic differentiation ability, gradually becoming important seed cells for jaw defect repair. However, the mandible has a complex bony structure and less cancellous content than appendicular bones. It is difficult to acquire a large number of high-quality jaw-derived marrow mesenchymal stem cells using traditional methods. This study presents a 'niche-based approach on stemness' for isolating and culturing rat jaw bone marrow mesenchymal stem cells (JBMMSCs). Primary rat JBMMSCs were isolated and cultured using the whole bone marrow adherent method combined with the bone slice digestion method. The isolated cells were identified as JBMMSCs through cell morphology observation, detection of cell surface markers, and multi-directional differentiation induction. The cells extracted by this method exhibit a 'fibroblast-like' spindle shape. The cells are long, spindle-shaped and fibroblast-like. The flow cytometry analysis shows these cells are positive for CD29, CD44, and CD90 but negative for CD11b/c, CD34, and CD45, which is congruent with BMMSCs characteristics. The cells show strong proliferation capacity and can undergo osteogenic, adipogenic, and chondrogenic differentiation. This study provides an effective and stable method for obtaining enough high-quality JBMMSCs with strong differentiation ability in a short time, which could facilitate further studies of the exploration of biological function, regenerative medicine, and related clinical applications.
Mesenchymal stem cells (MSCs) were first discovered in bone marrow, which showed the ability to form adhesive colonies in culture and strong osteogenic potential1. Pittinger et al.2 further found their multi-directional differentiation potential towards bone, fat, and cartilage. Although all mesenchymal stem cells from different sources have the potential for multi-directional differentiation, bone marrow mesenchymal stem cells have the strongest chondrogenic differentiation potential compared with mesenchymal stem cells derived from other tissues, making them considered the best candidate cells for bone tissue engineeri....
The protocol was approved by the Institutional Animal Ethics Committee of the Chinese PLA General Hospital. Thirteen-week-old male Wistar rats were used for the experiment. Details on the animals, reagents, and equipment are listed in the Table of Materials.
1. Experimental preparation
After 72 h of cell inoculation, most cells were suspended and round in shape, with very few adhered to the wall (Figure 1B). By the fifth day, adherent cell colonies appeared, exhibiting spindles or fibroblast-like shapes (Figure 1C). By the seventh day, adherent cells reached 90% confluency, forming a "fish school" shape with a small number of intermittent suspended cells (Figure 1D). Passaged cells grew rapidly and were pa.......
Bone marrow mesenchymal stem cells (BMMSCs) represent a subset of non-hematopoietic stem cells residing in bone marrow, characterized by their self-renewal capabilities, multi-directional differentiation potential, and supportive functions for hematopoiesis. These cells play pivotal roles in various physiological processes such as tissue regeneration, angiogenesis, and the regulation of cellular activities20. Consequently, BMMSCs are frequently utilized in tissue repair and regenerative engineerin.......
This study was supported by the Health Care Projects of the Military Commission Logistics Department (19BJZ22), Beijing Natural Science Foundation (7232154), and Fourth Mil Med Univ. clinical research projects (2021XB025).
....Name | Company | Catalog Number | Comments |
Alizarin Red S Solution 0.2% | Solarbio | G1450 | |
BCIP/NBT Alkaline Phosphatase Color Development Kit | Beyotime | C3206 | |
Bio-Rad CFX96 Real-Time System | Bio-Rad | ||
CCK8 Kit | Dujindo | CK04 | |
Cell culture dish 10 cm | Corning | 353003 | |
Centrifuge | Eppendorf | 5810R | |
Centrifuge Tube 15 mLÂ | Corning | 430790 | |
Centrifuge Tube 50 mLÂ | Corning | 430828 | |
CO2 incubator | Thermo Fisher | 3111 | |
Constant-temperature oscillator | Shanghai Zhicheng Analysis Instrument Manufacturing Co., Ltd. | ZWY-100H | |
Fetal bovine serum | BI | 04-001-1ACS | |
Flow cytometer | BD | FACS C6Â | |
Inverted phase-contrast microscope | Olympus | CKX41Â | |
Mesenchymal Stem Cell (Rat) Surface marker Detection Kit | Oricell | RAXMX-09011 | |
Multifunctional microplate reader | BioTek | Synergy LX Multi-Mode | |
Oil Red O Stain Kit | Solarbio | G1262 | |
Paraformaldehyde 4% | Solarbio | P1110 | |
PBS | MACGENE | CC008 | |
penicillin-streptomycin 0.25% | MACGENE | CC004 | |
PowerUp SYBR Green Master Mix | Thermo Fisher | A25742 | |
PrimeScript RT Master Mix | Takara | RR036A | |
Rat Bone Marrow Mesenchymal Stem Cells Adipogenic Differentiation kit | Oricell | RAXMX-90031 | |
Rat Bone Marrow Mesenchymal Stem Cells Chondrogenic Differentiation kit | Oricell | RAXMX-90041 | |
Rat Bone Marrow Mesenchymal Stem Cells Osteogenic Differentiation kit | Oricell | RAXMD-90021 | |
RNA extraction kit | TIANGEN | DP419 | |
Super-clean bench | Beijing Yataikelong Instrument Technology Co. Ltd. | KLCZ-1220A | |
Trypsin-EDTAÂ 0.25% | MACGENE | CC012 | |
Type II collagenase | Solarbio | C8150 | |
Wistar rat | Beijing Yataikelong Instrument Technology Co. Ltd. | ||
α-MEM culture medium | Gibco | C12571500BT |
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