Journal of Peking University (Health Sciences) ›› 2026, Vol. 58 ›› Issue (3): 641-649. doi: 10.19723/j.issn.1671-167X.2026.03.026

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Dynamic stretching promotes osteogenic differentiation of human bone marrow mesenchymal stem cells in three-dimensional culture

Xiaoqiang BAI1,2, Zhiruo YUAN2, Yongsheng ZHOU1,2,*(), Longwei LV2,3,*()   

  1. 1. Institute of Medical Technology, Peking University Health Science Center, Beijing 100191, China
    2. Department of Prosthodontics, Peking University School and Hospital of Stomatology & National Center for Stomatology & National Clinical Research Center for Oral Diseases & National Engineering Research Center of Oral Biomaterials and Digital Medical Devices & Beijing Key Laboratory for Intelligent Biomanufacturing and Regeneration of Craniofacial Tissues & NHC Key Laboratory of Digital Stomatology, Beijing 100081, China
    3. Peking University Hospital of Stomatology Sanya Division(Sanya Stomatology Center), Sanya 572013, Hainan, China
  • Received:2024-01-16 Online:2026-06-18 Published:2026-04-09
  • Contact: Yongsheng ZHOU, Longwei LV
  • Supported by:
    the National Natural Science Foundation of China(82271032); the National Natural Science Foundation of China(82470943); the Hainan Provincial Natural Science Foundation of China(825YXQN602); the Peking University Clinical Scientist Training Program(BMU2025PYJH011)

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Abstract:

Objective: To explore the promotion of dynamic distraction on osteogenic differentiation of human bone marrow mesenchymal stem cells (hBMMSCs) in three-dimensional culture. Methods: Dynamic stretching in a three-dimensional culture for hBMMSCs was achieved with proportions set at 5%, 10%, and 20%, a frequency of 0.5 Hz, and a dynamic stretching duration of 2 hours per day. Static culture was used as the control group. Deformation of hBMMSCs induced by dynamic stretching was observed through cytoplasmic fluorescence staining. After 7 days of dynamic stretching culture, the impact of dynamic stretching on the viability of hBMMSCs was observed through cell live/dead staining. The effect of dynamic stretching on the osteogenic differentiation of hBMMSCs was observed through alkaline phosphatase (ALP) staining and the expression of osteogenic related genes and proteins after 7 days of dynamic stretching culture. Results: Dynamic stretching in a three-dimensional culture for hBMMSCs was successfully constructed, which could achieve different durations, frequencies, and ratios of dynamic stretching. Dynamic stretching led to deformation of hBMMSCs, and the greater the stretching ratio, the more pronounced the cell deformation, transitioning from a circular to a flat oval shape. After 7 days of dynamic stretching culture, hBMMSCs in the static control group and dynamic stretching groups were mostly green stained live cells, with only a few red stained dead cells. The difference in the proportion of live cells between the groups was not statistically significant (P>0.05). The ALP staining in the dynamic stretching group was deeper than that in the static control group, and the number of ALP staining positive cells observed under the microscope was higher. The expression of osteogenic related genes and proteins increased after 7 days of dynamic stretching culture, and the difference was statistically significant (P < 0.05). Among them, the dynamic stretching group with 10% had the deepest ALP staining, the highest number of positive cells, and the most significant increase in the expression of osteogenic related genes and proteins compared with the static control group. Conclusion: Dynamic stretching caused deformation of hBMMSCs without a significant impact on cell viability, and it could effectively promote the osteogenic differentiation of hBMMSCs.

Key words: Dynamic stretching, Three-dimensional culture, Human bone marrow mesenchymal stem cells, Osteogenic differentiation

CLC Number: 

  • R78

Table 1

Prime sequences used for quantitative real-time PCR"

Gene Forward primer(5′to 3′) Reverse prime(5′to 3′)
GAPDH GAAGGTGAAGGTCGGAGTC GAAGATGGTGATGGGATTTC
RUNX2 GAACCACAAGTGCGGTGCAA ACTGCTTGCAGCCTTAAATGACT
ALP ATGGGATGGGTGTCTCCACA CCACGAAGGGGAACTTGTC
OCN CATGAGAGCCCTCACACTCCTC CCTGCTTGGACACAAAGGCTGC
COL-1 ACAGGGCTCTAATGATGTTGA AGGCGTGATGGCTTATTTGT

Figure 1

Construction of dynamic stretching three-dimensional culture hBMMSCs, human bone marrow mesenchymal stem cells; GelMA, gelatin methacryloyl."

Figure 2

Deformation of hBMMSCs under dynamic stretching at different proportions"

Figure 3

Live/dead staining (A) and the proportion of live cells (B) of hBMMSCs under dynamic stretching at different proportions hBMMSCs, human bone marrow mesenchymal stem cells; ns, not significant."

Figure 4

ALP staining' s general view (A), microscope view (B) and relative quantification of activity (C) of hBMMSCs under dynamic stretching at different proportions hBMMSCs, human bone marrow mesenchymal stem cells; ALP, alkaline phosphatase."

Figure 5

Expression of osteogenic related genes of hBMMSCs under dynamic stretching at different proportions hBMMSCs, human bone marrow mesenchymal stem cells; RUNX2, runt-related transcription factor 2 (A); ALP, alkaline phosphatase (B); OCN, osteocalcin (C); COL-1, collagen-1 (D)."

Figure 6

Expression of osteogenic related proteins RUNX2 underdynamic stretching at different proportions hBMMSCs, human bone marrow mesenchymal stem cells; RUNX2, runt-related transcription factor 2. DAPI, 4′, 6-diamidino-2-phenylindole."

Figure 7

Expression of osteogenic related proteins OCN under dynamic stretching at different proportions hBMMSCs, human bone marrow mesenchymal stem cells; OCN, osteocalcin. DAPI, 4′, 6-diamidino-2-phenylindole."

Figure 8

Expression of osteogenic related proteins COL-1 under dynamic stretching at different proportions hBMMSCs, human bone marrow mesenchymal stem cells; COL-1, collagen-1. DAPI, 4′, 6-diamidino-2-phenylindole."

Figure 9

Semi quantitative analysis of the expression of osteogenic related proteins RUNX2(A), OCN(B), and COL-1(C) of hBMMSCs under dynamic stretching at different proportions hBMMSCs, human bone marrow mesenchymal stem cells; RUNX2, runt-related transcription factor 2; OCN, osteocalcin; COL-1, collagen-1."

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