Department of Obstetrics and Gynecology, Meharry Medical College, Nashville, TN 37208, USA.
Hum Reprod. 2013 Sep;28(9):2407-16. doi: 10.1093/humrep/det265. Epub 2013 Jun 27.
Can biologically active vitamin D3 [1,25(OH)₂D3] regulate the expression and activity of matrix metalloproteinases (MMPs) in human uterine fibroid cells?
1,25(OH)₂D3 effectively reduced the expression and activities of MMP-2 and MMP-9 in cultured human uterine fibroid cells.
Uterine fibroids (leiomyoma) express higher levels of MMP activity than adjacent normal myometrium, and this is associated with uterine fibroid pathogenesis. However, it is unknown whether 1,25(OH)₂D3 can regulate the expression and activities of MMPs in human uterine fibroid cells.
STUDY DESIGN, SIZE, DURATION: Surgically removed fresh fibroid tissue was used to generate primary uterine fibroid cells.
PARTICIPANTS/MATERIALS, SETTING, METHODS: An immortalized human uterine fibroid cell line (HuLM) and/or primary human uterine fibroid cells isolated from fresh fibroid tissue were used to examine the expression of several MMPs, tissue inhibitors of metalloproteinases (TIMP) 1 and 2 and the activities of MMP-2 and MMP-9 after 1,25(OH)₂D3 treatment. Real-time PCR and western blots analyses were used to measure mRNA and protein expression of MMPs, respectively. Supernatant cell culture media were analyzed for MMP-2 and MMP-9 activities using a gelatin zymography assay.
1-1000 nM 1,25(OH)₂D3 significantly reduced mRNA levels of MMP-2 and MMP-9 in HuLM cells in a concentration-dependent manner (P < 0.5 to P < 0.001). The mRNA levels of MMP-1, MMP-3, MMP-13 and MMP-14 in HuLM cells were also reduced by 1,25(OH)₂D3. 1,25(OH)₂D3 significantly reduced MMP-2 and MMP-9 protein levels in a concentration-dependent manner in both HuLM and primary uterine fibroid cells (P < 0.05 to P < 0.001). Moreover, 1,25(OH)₂D3 increased the mRNA levels of vitamin D receptor (VDR) and TIMP-2 in a concentration-dependent manner in HuLM cells (P < 0.05 to P < 0.01). 1,25(OH)₂D3 also significantly increased protein levels of VDR and TIMP-2 in all cell types tested (P < 0.05 to P < 0.001). Gelatin zymography revealed that pro-MMP-2, active MMP-2 and pro-MMP-9 were down-regulated by 1,25(OH)₂D3 in a concentration-dependent manner; however, the active MMP-9 was undetectable.
LIMITATIONS, REASONS FOR CAUTION: This study was performed using in vitro uterine fibroid cell cultures and the results were extrapolated to in vivo situation of uterine fibroids. Moreover, in this study the interaction of vitamin D3 with other regulators such as steroid hormone receptors was not explored.
This study reveals an important biological function of 1,25(OH)₂D3 in the regulation of expression and activities of MMP-2 and MMP-9. Thus, 1,25(OH)₂D3 might be a potential effective, safe non-surgical treatment option for human uterine fibroids.
生物活性维生素 D3[1,25(OH)₂D3]能否调节人子宫肌瘤细胞中基质金属蛋白酶(MMPs)的表达和活性?
1,25(OH)₂D3 可有效降低培养的人子宫肌瘤细胞中 MMP-2 和 MMP-9 的表达和活性。
子宫肌瘤(平滑肌瘤)表达的 MMP 活性水平高于相邻的正常子宫肌层,这与子宫肌瘤的发病机制有关。然而,目前尚不清楚 1,25(OH)₂D3 是否可以调节人子宫肌瘤细胞中 MMPs 的表达和活性。
研究设计、大小、持续时间:使用手术切除的新鲜肌瘤组织生成原发性子宫肌瘤细胞。
参与者/材料、设置、方法:使用永生化人子宫肌瘤细胞系(HuLM)和/或从新鲜肌瘤组织中分离的原发性人子宫肌瘤细胞,研究 1,25(OH)₂D3 处理后几种 MMP、金属蛋白酶组织抑制剂(TIMP)1 和 2 以及 MMP-2 和 MMP-9 的活性的表达。实时 PCR 和 Western blot 分析分别用于测量 MMPs 的 mRNA 和蛋白表达。使用明胶酶谱法分析细胞培养上清液中 MMP-2 和 MMP-9 的活性。
1-1000 nM 1,25(OH)₂D3 以浓度依赖性方式显著降低 HuLM 细胞中 MMP-2 和 MMP-9 的 mRNA 水平(P < 0.5 至 P < 0.001)。1,25(OH)₂D3 还降低了 HuLM 细胞中 MMP-1、MMP-3、MMP-13 和 MMP-14 的 mRNA 水平。1,25(OH)₂D3 以浓度依赖性方式显著降低 HuLM 和原发性子宫肌瘤细胞中 MMP-2 和 MMP-9 的蛋白水平(P < 0.05 至 P < 0.001)。此外,1,25(OH)₂D3 以浓度依赖性方式增加 HuLM 细胞中维生素 D 受体(VDR)和 TIMP-2 的 mRNA 水平(P < 0.05 至 P < 0.01)。1,25(OH)₂D3 还显著增加了所有测试细胞类型中 VDR 和 TIMP-2 的蛋白水平(P < 0.05 至 P < 0.001)。明胶酶谱显示,1,25(OH)₂D3 以浓度依赖性方式下调 pro-MMP-2、活性 MMP-2 和 pro-MMP-9;然而,活性 MMP-9 无法检测到。
局限性、谨慎的原因:本研究使用体外子宫肌瘤细胞培养进行,结果推断为子宫肌瘤的体内情况。此外,在这项研究中,维生素 D3 与其他调节剂(如甾体激素受体)的相互作用未被探索。
本研究揭示了 1,25(OH)₂D3 在调节 MMP-2 和 MMP-9 的表达和活性方面的重要生物学功能。因此,1,25(OH)₂D3 可能是治疗人类子宫肌瘤的一种潜在有效、安全的非手术治疗选择。