Monnouchi S, Maeda H, Yuda A, Hamano S, Wada N, Tomokiyo A, Koori K, Sugii H, Serita S, Akamine A
Division of Oral Rehabilitation, Department of Endodontology and Operative Dentistry, Faculty of Dental Science, Kyushu University, Fukuoka, Japan.
J Periodontal Res. 2015 Apr;50(2):231-9. doi: 10.1111/jre.12200. Epub 2014 Jun 20.
The periodontal ligament (PDL) is continually exposed to mechanical loading caused by mastication or occlusion. Physiological loading is thus considered a key regulator of PDL tissue homeostasis; however, it remains unclear how this occurs. We recently reported that an appropriate magnitude of mechanical stretch can maintain PDL tissue homeostasis via the renin-angiotensin system. In the present study, we investigated the expression of interleukin-11 (IL-11) in human primary PDL cells (HPDLCs) exposed to stretch loading, the contribution of angiotensin II (Ang II) to this event and the effects of IL-11 on osteoblastic/cementoblastic differentiation of human PDL progenitor cells (cell line 1-17).
Human primary PDL cells, derived from human tissues, with or without antagonists against the Ang II receptors AT1 or AT2, were subjected to cyclical stretch loading with 8% elongation for 1 h. Expression of IL-11 was measured by ELISA in these cultures and by immunohistochemistry in the sectioned maxillae of rats. The osteoblastic/cementoblastic potential of cell line 1-17 was determined using cell proliferation, gene expression and Alizarin Red staining.
Positive staining for IL-11 was observed in the PDL of rat maxillae and in cultures of HPDLCs. In HPDLCs exposed to stretch, expression of the IL11 gene and the IL-11 protein were up-regulated, concomitant with an increase in Ang II and via AT2. Recombinant human IL-11 (rhIL-11) stimulated an increase in expression of mRNA for the cementoblast-specific marker, CP-23, and for the osteoblastic markers, osteopontin and bone sialoprotein, and promoted proliferation in cell line 1-17. In addition, rhIL-11 also increased the degree of mineralized nodule formation in cell line 1-17 cultures treated with CaCl2 .
Mechanical loading appears to control proliferation and osteoblastic/cementoblastic differentiation of human PDL stem/progenitor cells through the regulation of Ang II and AT2 by IL-11.
牙周韧带(PDL)持续受到咀嚼或咬合引起的机械负荷。因此,生理负荷被认为是PDL组织稳态的关键调节因子;然而,其具体机制尚不清楚。我们最近报道,适当强度的机械拉伸可通过肾素-血管紧张素系统维持PDL组织稳态。在本研究中,我们调查了拉伸负荷下人原代PDL细胞(HPDLCs)中白细胞介素-11(IL-11)的表达、血管紧张素II(Ang II)在此过程中的作用以及IL-11对人PDL祖细胞(细胞系1-17)成骨/成牙骨质细胞分化的影响。
源自人体组织的人原代PDL细胞,在有或没有Ang II受体AT1或AT2拮抗剂的情况下,以8%的伸长率进行1小时的周期性拉伸负荷处理。通过ELISA检测这些培养物中IL-11的表达,并通过免疫组织化学检测大鼠上颌骨切片中的表达。使用细胞增殖、基因表达和茜素红染色来确定细胞系1-17的成骨/成牙骨质潜能。
在大鼠上颌骨的PDL和HPDLCs培养物中观察到IL-11的阳性染色。在暴露于拉伸的HPDLCs中,IL11基因和IL-11蛋白的表达上调,同时Ang II增加并通过AT2。重组人IL-11(rhIL-11)刺激成牙骨质细胞特异性标志物CP-23以及成骨标志物骨桥蛋白和骨唾液蛋白的mRNA表达增加,并促进细胞系1-17的增殖。此外,rhIL-11还增加了用CaCl2处理的细胞系1-17培养物中矿化结节的形成程度。
机械负荷似乎通过IL-11对Ang II和AT2的调节来控制人PDL干/祖细胞的增殖和成骨/成牙骨质细胞分化。