
浏览全部资源
扫码关注微信
1.山西医科大学基础医学院生物化学与分子生物学教研室,太原 030001
2.山西白求恩医院内分泌科,太原 030032
3.太原市中心医院内分泌科,太原 030009
卫莹,Email:15234707831@163.com,研究方向:内分泌代谢病基础与临床研究。
刘师伟,Email:lswspring6@aliyun.com。
纸质出版日期:2022-05-28,
收稿日期:2021-05-15,
扫 描 看 全 文
卫莹, 刘师伟, 段瑞雪, 等. 人脐带间充质干细胞通过调控OPG/RANKL比值对骨质疏松大鼠的影响及机制研究[J]. 重庆医科大学学报, 2022,47(5):503-510.
Ying Wei, Shiwei Liu, Ruixue Duan, et al. Effects and mechanism of human umbilical cord mesenchymal stem cells on osteoporosis rats by regulating the ratio of osteoprotegerin/receptor activator of nuclear factor-κB ligand[J]. Journal of Shanxi Agricultural Sciences, 2022,47(5):503-510.
卫莹, 刘师伟, 段瑞雪, 等. 人脐带间充质干细胞通过调控OPG/RANKL比值对骨质疏松大鼠的影响及机制研究[J]. 重庆医科大学学报, 2022,47(5):503-510. DOI: 10.13406/j.cnki.cyxb.002972.
Ying Wei, Shiwei Liu, Ruixue Duan, et al. Effects and mechanism of human umbilical cord mesenchymal stem cells on osteoporosis rats by regulating the ratio of osteoprotegerin/receptor activator of nuclear factor-κB ligand[J]. Journal of Shanxi Agricultural Sciences, 2022,47(5):503-510. DOI: 10.13406/j.cnki.cyxb.002972.
目的:
2
探讨人脐带间充质干细胞(human umbilical cord mesenchymal stem cells,HUC-MSCs)对骨质疏松大鼠的影响及机制。
方法:
2
将30只SPF级6月龄雌性SD大鼠随机分为3组:假手术组(Sham组)、卵巢切除组(OVX组)、卵巢切除+HUC-MSCs干预组(4×10
6
/3 d,HUC-MSCs干预组),每组各10只,Sham组切除大鼠腹腔少量脂肪,其余各组均去除双侧卵巢建立骨质疏松大鼠模型。建模成功后,HUC-MSCs组用干细胞干预12周,其余2组用等剂量生理盐水干预。干预结束后,通过骨代谢血清指标血钙(calcium,Ca)、血磷(phosphorus,P)、碱性磷酸酶(alkaline phosphatase,ALP)、Ⅰ型胶原C端肽(c-terminal peptide of typeⅠcollagen,CTX)、骨组织形态计量学参数测量、骨密度检测、成骨细胞表面积/骨表面积比(osteoblast surface/bone surface,ObS/BS)和破骨细胞表面积/骨表面积比(osteoclast surface area/bone surface,OcS/BS),评估大鼠骨质疏松改善情况,同时通过Western blot探究各组大鼠骨保护素(osteoprotegerin,OPG)/核因子-κB受体活化因子配体(receptor activator of nuclear factor-κB ligand,RANKL)、β-连环蛋白(β-catenin)、Runt相关转录因子2(Runt-related transcription factor 2,Runx2)的表达情况。
结果:
2
HUC-MSCs组大鼠血清Ca、ALP含量明显高于OVX组(2.320±0.188 vs.1.822±0.139;79.584±8.349 vs.43.644±5.369;均
P
=0.000),P、CTX含量明显低于OVX组(1.651±0.068 vs.1.864±0.076,
P
=0.000;119.832±18.180 vs.144.272±15.629,
P
=0.039);HUC-MSCs组骨小梁结构得到明显改善,骨密度、骨小梁数目、骨小梁面积比、ObS/BS均明显高于OVX组(161.114±16.726 vs.126.558±7.100,
P
=0.009;1.702±0.220 vs.1.051±0.323,
P
=0.020;33.111±6.101 vs.19.575±5.629,
P
=0.022;45.279±3.947 vs.33.948±7.339,
P
=0.041),骨小梁分离度、OcS/BS明显低于OVX组(0.592±0.066 vs.0.845±0.165,
P
=0.018;37.532±3.910 vs.44.891±3.615,
P
=0.026);Western blot结果显示HUC-MSCs组OPG/RANKL比值、β-catenin、Runx2的蛋白表达量明显高于OVX组(0.776±0.045 vs.0.097±0.063,
P
=0.000;0.590±0.057 vs.0.202±0.088,
P
=0.000;0.595±0.078 vs.0.239±0.071,
P
=0.001)。
结论:
2
HUC-MSCs可以通过Wnt/β-catenin/Runx2通路调节OPG/RANKL比值,促进骨形成,抑制骨吸收,改善骨质疏松。
Objective
:
2
To investigate the effect of human umbilical cord mesenchymal stem cells (HUC-MSCs) on osteoporosis rats and its mechanism.
Methods
:
2
Thirty SPF grade 6-month-old female rats were randomly divided into three groups: sham operation group (Sham group)
ovariectomy group (OVX group) and HUC-MSCs intervention group (HUC-MSCs group) (4×10
6
/3 day)
with 10 rats in each group. In Sham group
a small amount of abdominal fat was removed
and the other groups were removed bilateral ovaries to establish osteoporosis rat model. After successful modeling
HUC-MSCs group was intervened with stem cells for 12 w
while the other two groups were intervened with equal dose of normal saline. After the intervention
calcium (Ca)
phosphorus (P)
alkaline phosphatase (ALP)
c-terminal peptide of type I collagen (CTX)
histomorphometric parameters of femur
bone mineral density (BMD)
osteoblast surface/bone surface ratio (ObS/BS) and osteoclast surface area/bone surface (OcS/BS) were used to evaluate the improvement of osteoporosis in rats. Meanwhile
the expression of osteoprotegerin (OPG)
receptor activator of nuclear factor-κB ligand (RANKL)
β-catenin and Runt-related transcription factor 2 (Runx2) were detected by Western blot.
Results
:
2
The contents of serum Ca and ALP in HUC-MSCs group were significantly higher than those in OVX group (2.320±0.188 vs.1.822±0.139; 79.584±8.349 vs.43.644±5.369; all
P
=0.000) ; P and CTX contents were significantly lower than those in OVX group (1.651±0.068 vs.1.864±0.076
P
=0.000; 119.832±18.180 vs.144.272±15.629
P
=0.039) ; BMD
the number of trabecular bone
the ratio of trabecular area and ObS/BS in HUC-MSCs group were significantly higher than those in OVX group (161.114±16.726 vs.126.558±7.100
P
=0.009; 1.702±0.220 vs.1.051±0.323
P
=0.020; 33.111±6.101 vs.19.575±5.629
P
=0.022; 45.279±3.947 vs.33.948±7.339
P
=0.041) ; the bone trabecular separation and OcS/BS in HUC-MSCs group were significantly lower than those in OVX group (0.592±0.066 vs.0.845±0.165
P
=0.018; 37.532±3.910 vs.44.891±3.615
P
=0.026) ; the results of Western blot showed that the ratio of OPG/RANKL and the protein expression of β-catenin and Runx2 in HUC-MSCs group were significantly higher than those in OVX group (0.776±0.045 vs.0.097±0.063
P
=0.000; 0.590±0.057 vs.0.202±0.088
P
=0.000; 0.595±0.078 vs.0.239±0.071
P
=0.001) .
Conclusion
:
2
HUC-MSCs can regulate OPG/RANKL ratio through Wnt/β-catenin/Runx2 pathway
thus promoting bone formation
inhibiting bone resorption and improving osteoporosis.
骨质疏松人脐带间充质干细胞骨代谢骨保护素/核因子-κB受体活化因子配体
osteoporosishuman umbilical cord mesenchymal stem cellbone metabolismosteoprotegerin/receptor activator of nuclear factor-κB ligand
Leslie WD, Morin SN. Osteoporosis epidemiology 2013: implications for diagnosis, risk assessment, and treatment[J]. Curr Opin Rheumatol, 2014, 26(4): 440-446.
Chen P, Li ZZ, Hu YH. Prevalence of osteoporosis in China: a meta-analysis and systematic review[J]. BMC Public Health, 2016, 16(1): 1039.
Beekman KM, Veldhuis-Vlug AG, den Heijer M, et al. The effect of raloxifene on bone marrow adipose tissue and bone turnover in postmenopausal women with osteoporosis[J]. Bone, 2019, 118: 62-68.
刘秋英, 利奕成, 何绍清, 等. 脐带间充质干细胞治疗大鼠骨质疏松的初步研究[J]. 中国细胞生物学学报, 2013, 35(11): 1592-1597.
Liu QY, Li YC, He SQ, et al. Effect of umbilical cord mesenchymal stem cell transplanting on retinoicacid-induced osteoporosis in rats[J]. Chin J Cell Biol, 2013, 35(11): 1592-1597.
Al-Nbaheen M, Vishnubalaji R, Ali DL, et al. Human stromal (mesenchymal) stem cells from bone marrow, adipose tissue and skin exhibit differences in molecular phenotype and differentiation potential[J]. Stem Cell Rev Rep, 2013, 9(1): 32-43.
Santos JM, Bárcia RN, Simões SI, et al. The role of human umbilical cord tissue-derived mesenchymal stromal cells (UCX®) in the treatment of inflammatory arthritis[J]. J Transl Med, 2013, 11: 18.
姚映灵, 何玲, 毕杨, 等. 人滑膜间充质干细胞与人脐带间充质干细胞的生物学性状比较[J]. 中国细胞生物学学报, 2021, 43(2): 302-310.
Yao YL, He L, Bi Y, et al. Comparison of biological characteristics of human synovial mesenchymal stem cells and human umbilical cord mesenchymal stem cells[J]. Chin J Cell Biol, 2021, 43(2): 302-310.
Rodríguez JP, Garat S, Gajardo H, et al. Abnormal osteogenesis in osteoporotic patients is reflected by altered mesenchymal stem cells dynamics[J]. J Cell Biochem, 1999, 75(3): 414-423.
黄健萍, 林思恩, 吴玲芝, 等. 复方脑复康预防大鼠去卵巢后骨质疏松的研究[J]. 重庆医科大学学报, 2011, 36(11): 1292-1295.
Huang JP, Lin SE, Wu LZ, et al. Effects of compound piracetam in preventing osteoporosis in ovariectomized rats[J]. J Chongqing Med Univ, 2011, 36(11): 1292-1295.
Liang M, Liu WG, Peng ZB, et al. The therapeutic effect of secretome from human umbilical cord-derived mesenchymal stem cells in age-related osteoporosis[J]. Artif Cells Nanomed Biotechnol, 2019, 47(1): 1357-1366.
Ezquerra S, Zuleta A, Arancibia R, et al. Functional properties of human-derived mesenchymal stem cell spheroids: a meta-analysis and systematic review[J]. Stem Cells Int, 2021, 2021: 8825332.
Ekram S, Khalid S, Bashir I, et al. Human umbilical cord-derived mesenchymal stem cells and their chondroprogenitor derivatives reduced pain and inflammation signaling and promote regeneration in a rat intervertebral disc degeneration model[J]. Mol Cell Biochem, 2021, 476(8): 3191-3205.
Semenova E, Grudniak MP, Machaj EK, et al. Mesenchymal stromal cells from different parts of umbilical cord: approach to comparison& characteristics[J]. Stem Cell Rev Rep, 2021, 17(5): 1780-1795.
Bertoni L, Jacquet-Guibon S, Branly T, et al. Evaluation of allogeneic bone-marrow-derived and umbilical cord blood-derived mesenchymal stem cells to prevent the development of osteoarthritis in an equine model[J]. Int J Mol Sci, 2021, 22(5): 2499.
Tang L, Gao XH, Yang XY, et al. Ladder-climbing training prevents bone loss and microarchitecture deterioration in diet-induced obese rats[J]. Calcif Tissue Int, 2016, 98(1): 85-93.
An JH, Park H, Song JA, et al. Transplantation of human umbilical cord blood-derived mesenchymal stem cells or their conditioned medium prevents bone loss in ovariectomized nude mice[J]. Tissue Eng Part A, 2013, 19(5/6): 685-696.
Vasikaran S, Eastell R, Bruyère O, et al. Markers of bone turnover for the prediction of fracture risk and monitoring of osteoporosis treatment: a need for international reference standards[J]. Osteoporos Int, 2011, 22(2): 391-420.
Williams C, Sapra A. Osteoporosis markers[M]//StatPearls[Internet]. Treasure Island (FL): StatPearls Publising, 2021.
Hong B, Lee S, Shin N, et al. Bone regeneration with umbilical cord blood mesenchymal stem cells in femoral defects of ovariectomized rats[J]. Osteoporos Sarcopenia, 2018, 4(3): 95-101.
Fu YS, Lu CH, Chu KA, et al. Xenograft of human umbilical mesenchymal stem cells from wharton's jelly differentiating into osteocytes and reducing osteoclast activity reverses osteoporosis in ovariectomized rats[J]. Cell Transplant, 2018, 27(1): 194-208.
李苏华, 李惠, 廖湘平, 等. NGAL、OPG、RANKL及DAS28对RA骨质疏松的预测作用[J]. 重庆医科大学学报, 2019, 44(9): 1155-1158.
Li SH, Li H, Liao XP, et al. Value of neutrophil gelatinase-associated lipocalin, osteoprotegerin, receptor activator of nuclear factor-kappa B ligand, and 28-joint disease activity score in predicting osteoporosis in patients with rheumatoid arthritis[J]. J Chongqing Med Univ, 2019, 44(9): 1155-1158.
Mountzios G, Dimopoulos MA, Bamias A, et al. Abnormal bone remodeling process is due to an imbalance in the receptor activator of nuclear factor-κB ligand (RANKL)/osteoprotegerin (OPG) axis in patients with solid tumors metastatic to the skeleton[J]. Acta Oncol, 2007, 46(2): 221-229.
Yang G, Kim YN, Kim H, et al. Effect of human umbilical cord matrix-derived mesenchymal stem cells on bisphosphonate-related osteonecrosis of the jaw[J]. Tissue Eng Regen Med, 2021, 18(6): 975-988.
Yang N, Liu DK, Zhang X, et al. Effects of ginsenosides on bone remodelling for novel drug applications: a review[J]. Chin Med, 2020, 15: 42.
Han NN, Zheng Y, Li R, et al. β-catenin enhances odontoblastic differentiation of dental pulp cells through activation of Runx2[J]. PLoS One, 2014, 9(2): e88890.
Yin YK, Ding LX, Hou Y, et al. Upregulating microRNA-410 or downregulating Wnt-11 increases osteoblasts and reduces osteoclasts to alleviate osteonecrosis of the femoral head[J]. Nanoscale Res Lett, 2019, 14(1): 383.
Liu GZ, Vijayakumar S, Grumolato L, et al. Canonical Wnts function as potent regulators of osteogenesis by human mesenchymal stem cells[J]. J Cell Biol, 2009, 185(1): 67-75.
Bae YK, Kwon JH, Kim M, et al. Intracellular calcium determines the adipogenic differentiation potential of human umbilical cord blood-derived mesenchymal stem cells via the Wnt5a/β-catenin signaling pathway[J]. Stem Cells Int, 2018, 2018: 6545071.
0
浏览量
0
下载量
0
CSCD
关联资源
相关文章
相关作者
相关机构
京公网安备11010802024621