Kuh Sung Uk, Zhu Yerun, Li Jun, Tsai Kai-Jow, Fei Qinming, Hutton William C, Yoon S Tim
Department of Neurosurgery, The Spine and Spinal cord Institute, Yonsei University Medical College, Seoul, Korea.
Acta Neurochir (Wien). 2008 Oct;150(10):1073-9; discussion 1079. doi: 10.1007/s00701-008-0029-z. Epub 2008 Sep 10.
The recombinant human bone morphogenic protein-2 (rhBMP-2) is known to increase the proteoglycan production and chondrogenic gene expression in the disc cells. The transforming growth factor-beta 1 (TGF-beta(1)) can transform the bone marrow stem cells (BMDCs) into the disc-like cells.
We carried out an experiment to determine if TGF-beta(1) and rhBMP-2 can act in synergy on BMDCs by increasing the production of sulfated-glycosaminoglycan (sGAG) and affecting the mRNA expression of aggrecan, type I collagen, and type II collagen. The BMDCs were isolated from the iliac crest and femur of a New Zealand white rabbit (1 year). The BMDCs were culured in monolayer and treated for 6 days with TGF-beta(1) 10 ng/ml (group 1), rhBMP-2 200 ng/ml (group 2), and both TGF-beta(1) 10 ng/ml and rhBMP-2 200 ng/ml (group 3: the combined group) in Dulbecco's modified Eagle medium/F-12 with 1% fetal bovine serum. After 6 days, the sGAG content in the media was quantified using 1,9-dimethylmethylene blue staining and the mRNA expression of aggrecan, type I collagen, type II collagen, Sox-9, BMP-2, and BMP-7 were measured with the real-time PCR. The same BMDCs were also cultured in the chamber slide at 3 x 10(4) cells/chamber. After 6 days treatment, the treated cells were immunofluorescence stained with aggrecan, type I collagen, type II collagen, anti-BMP-2, anti-BMP-7 antibodies. After that, we compared the number of positive immunofluorescence stained cells with fluorescence microscope. The sGAG production and mRNA expression for each group were normalized against the same parameters for a non-treatment group.
The sGAG production was increased 1.15*, 1.34*, and 1.45* times in the TGF-beta(1) 10 ng/ml group, the rhBMP-2 200 ng/ml group, and the combined group respectively. The mRNA expression of aggrecan was increased 1.28, 3.42*, and 5.34* times, the mRNA expression of type I collagen was increased 0.86, 1.09, 1.17 times, the mRNA expression of type II collagen was increased 3.58*, 3.77*, and 10.78* times, the mRNA expression of Sox-9 was increased 1.29, 2.45, 2.75* times, the mRNA expression of BMP-2 was increased 1.14, 2.07, 4.43* times, and the mRNA expression of BMP-7 was increased 1.16, 1.49, 1.97* times, respectively for each group (* indicates p < 0.05). On the immunofluorescence staining of antibodies, the average positively immunofluorescence stained cells number for aggrecan were 4.2, 15.8*, 10*, and 22* according to the non-treatment group, TGF-beta(1) 10 ng/ml group, rhBMP-2 200 ng/ml group, and the combined group respectively. The average positively immunofluorescence stained cells number for type I collagen were 7, 14.2*, 9.2*, 17.4* and the average positively immunofluorescence stained cells number for type II collagen were 8.5, 28.25*, 20.25*, 42.25* and the average positively immunofluorescence stained cells number for anti-BMP-2 were 5, 16.75*, 8.75*, 27.25* and the average positively immunofluorescence stained cells number for anti-BMP-7 were 3.25, 7.5*, 8.75*, 15.25* (* indicates p < 0.05).
Both TGF-beta(1) and rhBMP-2 alone, can increase proteoglycan production in the BMDCs. However, if they were used in combination, there is a synergistic effect. Similarly, the mRNA expressions of both aggrecan, type II collagen, Sox-9, BMP-2, and BMP-7 except for type I collagen were increased significantly when TGF-beta(1) and rhBMP-2 were combined. The positive immunofluorescence stained cell numbers for aggrecan, type I, II collagen, BMP-2 and BMP-7 were also increased after each TGF-beta(1) and rhBMP-2 treatment, and also more increased significantly in the aggrecan, type I, II collagen, BMP-2, and 7 when they were used jointly.
已知重组人骨形态发生蛋白-2(rhBMP-2)可增加椎间盘细胞中蛋白聚糖的产生和软骨生成基因的表达。转化生长因子-β1(TGF-β1)可将骨髓干细胞(BMDCs)转化为椎间盘样细胞。
我们进行了一项实验,以确定TGF-β1和rhBMP-2是否能通过增加硫酸化糖胺聚糖(sGAG)的产生并影响聚集蛋白聚糖、I型胶原和II型胶原的mRNA表达,对BMDCs发挥协同作用。从1岁新西兰白兔的髂嵴和股骨中分离出BMDCs。将BMDCs进行单层培养,并在含有1%胎牛血清的杜尔贝科改良伊格尔培养基/F-12中,分别用10 ng/ml TGF-β1(第1组)、200 ng/ml rhBMP-2(第2组)以及10 ng/ml TGF-β1和200 ng/ml rhBMP-2(第3组:联合组)处理6天。6天后,使用1,9-二甲基亚甲基蓝染色法对培养基中的sGAG含量进行定量,并通过实时PCR检测聚集蛋白聚糖、I型胶原、II型胶原、Sox-9、BMP-2和BMP-7的mRNA表达。同样的BMDCs也以3×10⁴个细胞/孔的密度接种于细胞培养载玻片上。经过6天处理后,用聚集蛋白聚糖、I型胶原、II型胶原、抗BMP-2、抗BMP-7抗体对处理后的细胞进行免疫荧光染色。之后,用荧光显微镜比较阳性免疫荧光染色细胞的数量。将每组的sGAG产生量和mRNA表达量相对于未处理组的相同参数进行标准化。
在10 ng/ml TGF-β1组、200 ng/ml rhBMP-2组和联合组中,sGAG的产生量分别增加了1.15倍、1.34倍和1.45倍。聚集蛋白聚糖的mRNA表达分别增加了1.28倍、3.42倍和5.34倍,I型胶原的mRNA表达分别增加了0.86倍、1.09倍和1.17倍,II型胶原的mRNA表达分别增加了3.58倍、3.77倍和10.78倍,Sox-9的mRNA表达分别增加了1.29倍、2.45倍和2.75倍,BMP-2的mRNA表达分别增加了1.14倍、2.07倍和4.43倍,BMP-7的mRNA表达分别增加了1.16倍、1.49倍和1.97倍(*表示p<0.05)。在抗体免疫荧光染色方面,根据未处理组、10 ng/ml TGF-β1组、200 ng/ml rhBMP-2组和联合组的顺序,聚集蛋白聚糖的平均阳性免疫荧光染色细胞数分别为每视野4.2个、15.8个、10个和22个。I型胶原的平均阳性免疫荧光染色细胞数分别为7个、14.2个、9.2个和17.4个,II型胶原的平均阳性免疫荧光染色细胞数分别为8.5个、28.25个、20.25个和42.25个,抗BMP-2的平均阳性免疫荧光染色细胞数分别为5个、16.75个、8.75个和27.25个,抗BMP-7的平均阳性免疫荧光染色细胞数分别为3.25个、7.5个、8.75个和15.25个(*表示p<0.05)。
单独使用TGF-β1和rhBMP-2均可增加BMDCs中蛋白聚糖的产生。然而,若将它们联合使用,则存在协同效应。同样,当TGF-β1和rhBMP-2联合使用时,除I型胶原外,聚集蛋白聚糖、II型胶原、Sox-9、BMP-2和BMP-7的mRNA表达均显著增加。在每次TGF-β1和rhBMP-2处理后,聚集蛋白聚糖、I型、II型胶原、BMP-2和BMP-7的阳性免疫荧光染色细胞数也增加,并且当它们联合使用时,聚集蛋白聚糖、I型、II型胶原、BMP-2和7的阳性免疫荧光染色细胞数增加更为显著。