Kumamoto H, Ooya K
Division of Oral Pathology, Department of Oral Medicine and Surgery, Tohoku University Graduate School of Dentistry, Sendai, Japan.
Oral Dis. 2006 Mar;12(2):163-70. doi: 10.1111/j.1601-0825.2005.01177.x.
To further clarify the roles of regulators of embryonic development, bone morphogenetic protein (BMPs) and their associated molecules, in oncogenesis and cytodifferentiation of odontogenic tumors, the expression of these regulator molecules were analyzed in epithelial odontogenic tumors as well as in tooth germs.
Tooth germs, ameloblastomas, adenomatoid odontogenic tumors, and malignant ameloblastomas were examined by RT-PCR and immunohistochemistry for detection of BMP-2, -4, -7, BMP receptors I and II (BMPR-I, BMPR-II), core-binding factor alpha1 (CBFA1), and osterix.
mRNA expression of BMPs, BMPRs, CBFA1, and osterix was detected in all odontogenic tissues. Immunohistochemical reactivity for BMPs, BMPRs, and CBFA1 was detected in both epithelial and mesenchymal cells of tooth germs and epithelial odontogenic tumors. BMPs and BMPRs were evidently expressed in odontogenic epithelial cells in tooth germs and epithelial odontogenic tumors. Acanthomatous ameloblastomas showed increased BMP-7 reactivity in keratinizing cells. Nuclear CBFA1 expression was detected scatteredly in odontogenic epithelial cells in normal and neoplastic odontogenic tissues, as well as in some mesenchymal cells in tooth germs and in some stromal cells in epithelial odontogenic tumors. Ameloblastic carcinomas showed low reactivity for BMPs, BMPRs, and CBFA1.
BMPs and their associated molecules might play a role in cytodifferentiation of normal and neoplastic odontogenic epithelium via epithelial-mesenchymal interactions.
为了进一步阐明胚胎发育调节因子骨形态发生蛋白(BMPs)及其相关分子在牙源性肿瘤发生和细胞分化中的作用,对这些调节分子在上皮性牙源性肿瘤以及牙胚中的表达进行了分析。
采用逆转录聚合酶链反应(RT-PCR)和免疫组织化学方法检测牙胚、成釉细胞瘤、腺样牙源性肿瘤和恶性成釉细胞瘤中BMP-2、-4、-7、BMP受体I和II(BMPR-I、BMPR-II)、核心结合因子α1(CBFA1)和osterix的表达。
在所有牙源性组织中均检测到BMPs、BMPRs、CBFA1和osterix的mRNA表达。在牙胚和上皮性牙源性肿瘤的上皮细胞和间充质细胞中均检测到BMPs、BMPRs和CBFA1的免疫组织化学反应。BMPs和BMPRs在牙胚和上皮性牙源性肿瘤的牙源性上皮细胞中明显表达。棘皮瘤型成釉细胞瘤在角化细胞中BMP-7反应性增强。在正常和肿瘤性牙源性组织的牙源性上皮细胞中,以及在牙胚的一些间充质细胞和上皮性牙源性肿瘤的一些基质细胞中,散在检测到核CBFA1表达。成釉细胞癌对BMPs、BMPRs和CBFA1的反应性较低。
BMPs及其相关分子可能通过上皮-间充质相互作用在正常和肿瘤性牙源性上皮的细胞分化中发挥作用。