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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

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.

Abstract

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.

Introduction

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....

Protocol

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

  1. Sterilize all surgical instruments, including ophthalmic scissors, tweezers, and bone rongeurs, at high temperature and pressure.
  2. Prepare culture media in .......

Representative Results

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.......

Discussion

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.......

Acknowledgements

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).

....

Materials

NameCompanyCatalog NumberComments
Alizarin Red S Solution 0.2%SolarbioG1450
BCIP/NBT Alkaline Phosphatase Color Development KitBeyotimeC3206
Bio-Rad CFX96 Real-Time SystemBio-Rad
CCK8 KitDujindoCK04
Cell culture dish 10 cmCorning353003
CentrifugeEppendorf5810R
Centrifuge Tube 15 mL Corning430790
Centrifuge Tube 50 mL Corning430828
CO2 incubatorThermo Fisher3111
Constant-temperature oscillatorShanghai Zhicheng Analysis Instrument Manufacturing Co., Ltd.ZWY-100H
Fetal bovine serumBI04-001-1ACS
Flow cytometerBDFACS C6 
Inverted phase-contrast microscopeOlympusCKX41 
Mesenchymal Stem Cell (Rat) Surface marker Detection Kit OricellRAXMX-09011
Multifunctional microplate reader BioTekSynergy LX Multi-Mode
Oil Red O Stain KitSolarbioG1262
Paraformaldehyde 4%SolarbioP1110
PBSMACGENECC008
penicillin-streptomycin 0.25%MACGENECC004
PowerUp SYBR Green Master MixThermo Fisher A25742
PrimeScript RT Master Mix TakaraRR036A
Rat Bone Marrow Mesenchymal Stem Cells Adipogenic Differentiation kitOricellRAXMX-90031
Rat Bone Marrow Mesenchymal Stem Cells Chondrogenic Differentiation kitOricellRAXMX-90041
Rat Bone Marrow Mesenchymal Stem Cells Osteogenic Differentiation kitOricellRAXMD-90021
RNA extraction kitTIANGENDP419
Super-clean benchBeijing Yataikelong Instrument Technology Co. Ltd.KLCZ-1220A
Trypsin-EDTA  0.25%MACGENECC012
Type II collagenaseSolarbioC8150
Wistar ratBeijing Yataikelong Instrument Technology Co. Ltd.
α-MEM culture medium GibcoC12571500BT

References

  1. Friedenstein, A. J., Petrakova, K. V., Kurolesova, A. I., Frolova, G. P. Heterotopic of bone marrow. Analysis of precursor cells for osteogenic and hematopoietic tissues. Transplantation. 6 (2), 230-247 (1968).
  2. Pittenger, M. F., et al.

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MedicineMarrowMesenchymal Stem CellsIsolationCultureNiche based ApproachStemnessAppendicular BonesProliferationMulti directional DifferentiationOsteogenicAdipogenicChondrogenic

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