Kubota Y, Ninomiya T, Oka S, Takenoshita Y, Shirasuna K
Second Department of Oral and Maxillofacial Surgery, Faculty of Dentistry, Kyushu University, Fukuoka, Japan.
J Dent Res. 2000 Jun;79(6):1423-30. doi: 10.1177/00220345000790061201.
Interleukin-1alpha (IL-1alpha) and matrix metalloproteinase-9 (MMP-9) are thought to be involved in odontogenic cyst expansion. In this study, we investigated the effects of IL-1alpha on the secretion and activation of MMP-9 in odontogenic jaw cysts. An active form of MMP-9 was present in odontogenic keratocyst (6 of 8 cases) fluids more frequently than dentigerous cyst (3 of 10 cases) and radicular cyst (3 of 10 cases) fluids, although proMMP-9 was present in all cyst fluids. Odontogenic keratocyst fragments in explant culture secreted a larger amount of IL-1alpha than dentigerous cyst and radicular cyst fragments in explant culture, and spontaneously secreted both proMMP-9 and an active form of MMP-9. The fragments of dentigerous cysts and radicular cysts secreted a small amount of proMMP-9, but no active form of MMP-9. Exogenously added recombinant human IL-1alpha (rhlL-1alpha) increased the secretion and activation of proMMP-9 in the fragments of dentigerous cysts and radicular cysts. The epithelial cells isolated from odontogenic keratocysts secreted IL-1alpha and proMMP-9 without stimulation. Under the cultivation on a fibronectin-coated dish, rhIL-1alpha increased the secretion of proMMP-9 from the epithelial cells in a dose-dependent manner. Moreover, rhIL-1alpha induced the secretion of proMMP-3 and plasminogen activator urokinase (u-PA) from the epithelial cells, and converted the secreted proMMP-3 to the active form in the presence of plasminogen. The secreted proMMP-9 was also activated in the presence of rhIL-1alpha and plasminogen. Hence, our results suggest that IL-1alpha may up-regulate not only proMMP-9 secretion but also proMMP-9 activation by inducing proMMP-3 and u-PA production in the cyst epithelial cells by autocrine/paracrine regulatory mechanisms.
白细胞介素 -1α(IL -1α)和基质金属蛋白酶 -9(MMP -9)被认为与牙源性囊肿的扩大有关。在本研究中,我们调查了IL -1α对牙源性颌骨囊肿中MMP -9分泌和激活的影响。尽管所有囊肿液中均存在前MMP -9,但活性形式的MMP -9在牙源性角化囊肿(8例中的6例)液中出现的频率高于含牙囊肿(10例中的3例)和根尖囊肿(10例中的3例)液。外植体培养中的牙源性角化囊肿碎片比外植体培养中的含牙囊肿和根尖囊肿碎片分泌更多的IL -1α,并且自发分泌前MMP -9和活性形式的MMP -9。含牙囊肿和根尖囊肿的碎片分泌少量前MMP -9,但不分泌活性形式的MMP -9。外源添加的重组人IL -1α(rhIL -1α)增加了含牙囊肿和根尖囊肿碎片中前MMP -9的分泌和激活。从牙源性角化囊肿中分离的上皮细胞在无刺激情况下分泌IL -1α和前MMP -9。在纤连蛋白包被的培养皿上培养时,rhIL -1α以剂量依赖性方式增加上皮细胞前MMP -9的分泌。此外 rhIL -1α诱导上皮细胞分泌前MMP -3和纤溶酶原激活物尿激酶(u -PA),并在纤溶酶原存在的情况下将分泌的前MMP -3转化为活性形式。在rhIL -1α和纤溶酶原存在的情况下,分泌的前MMP -9也被激活。因此,我们的结果表明,IL -1α可能通过自分泌/旁分泌调节机制诱导囊肿上皮细胞中前MMP -3和u -PA的产生,不仅上调前MMP -9的分泌,还上调前MMP -9的激活。