Tang X, Meng H, Han J, Zhang L, Hou J, Zhang F
Department of Periodontology, Peking University School and Hospital of Stomatology, Beijing, China.
J Periodontal Res. 2008 Jun;43(3):311-21. doi: 10.1111/j.1600-0765.2007.01031.x. Epub 2007 Nov 13.
Estrogen has been shown to up-regulate the expression of osteoblastic phenotypes of human periodontal ligament cells via binding to estrogen receptors and may also help periodontal tissue regeneration. However, which subtype of estrogen receptor (alpha or beta) is predominately expressed in human periodontal ligament cells, and how estrogen receptor expression is regulated during the osteogenic differentiation of human periodontal ligament cells, is still unclear. This study aimed to explore the expression and regulation of estrogen receptor subtypes in human periodontal ligament cells and during their osteogenic differentiation.
Human periodontal ligament cells derived from 10 individual age-matched donors (five male and five female donors) were cultured. Human periodontal ligament cells under osteogenic induction (group M) and the corresponding controls (group C) were harvested on days 7, 14 and 21 for estrogen receptor detection.
Both estrogen receptor-alpha and estrogen receptor-beta mRNAs were expressed in human periodontal ligament cells from all of the 10 donors. Protein only of estrogen receptor-beta (not of estrogen receptor-alpha) was detected and was shown to be located in the nuclei of human periodontal ligament cells. The expression levels of estrogen receptor-beta mRNA and protein from both male and female donors in group M were significantly higher compared with group C during the 21-d study period. In comparison, the expression level of estrogen receptor-alpha mRNA of the donors was not significantly different from that of the controls during osteogenic differentiation and no estrogen receptor-alpha protein was detected.
The results suggest that estrogen receptor-beta may be the predominant subtype expressed in human periodontal ligament cells and may actively participate in the osteogenic differentiation process of human periodontal ligament cells, both in male and in female subjects.
雌激素已被证明可通过与雌激素受体结合上调人牙周膜细胞成骨细胞表型的表达,并且可能有助于牙周组织再生。然而,雌激素受体的哪种亚型(α或β)在人牙周膜细胞中占主导表达,以及在人牙周膜细胞成骨分化过程中雌激素受体表达是如何调控的,仍不清楚。本研究旨在探讨雌激素受体亚型在人牙周膜细胞及其成骨分化过程中的表达与调控。
培养来自10名年龄匹配个体(5名男性供体和5名女性供体)的人牙周膜细胞。在第7、14和21天收获成骨诱导下的人牙周膜细胞(M组)和相应的对照组(C组)用于雌激素受体检测。
10名供体的人牙周膜细胞中均表达雌激素受体α和雌激素受体β的mRNA。仅检测到雌激素受体β的蛋白(未检测到雌激素受体α的蛋白),且显示其位于人牙周膜细胞的细胞核中。在21天的研究期间,M组男性和女性供体的雌激素受体β mRNA和蛋白的表达水平均显著高于C组。相比之下,在成骨分化过程中,供体的雌激素受体α mRNA表达水平与对照组无显著差异,且未检测到雌激素受体α蛋白。
结果表明,雌激素受体β可能是在人牙周膜细胞中表达的主要亚型,并且可能在男性和女性受试者中均积极参与人牙周膜细胞的成骨分化过程。