Lin W L, McCulloch C A, Cho M I
Department of Oral Biology, School of Dental Medicine, State University of New York, Buffalo 14214.
Anat Rec. 1994 Dec;240(4):492-506. doi: 10.1002/ar.1092400407.
The entire socket after tooth extraction is filled with new bone formed by osteoblasts (Obs), but the origin of these Obs remains unknown. Thus, the proliferation and migration of paravascular and endosteal fibroblastic cells and periodontal ligament (PDL) fibroblasts (Fbs) and their differentiation into Obs during socket healing after extraction of the first maxillary molars of the rat were investigated.
The proliferative activity and migration of these cells in the sockets after tooth extraction were studied using radioautography and immunohistochemistry after injection of 3H-thymidine and 5-bromo-2'-deoxyuridine (BrdU), respectively. Their morphological changes during differentiation was investigated by transmission electron microscopy.
One day after tooth extraction, PDL Fbs were the major cell type in the PDL remnant of the socket. Proliferation was low (labeling index (LI) = approximately 2%) until 16 h after tooth extraction but dramatically increased to a maximum level 1 day postextraction (LI = 23%). Between 1 and 2 days, numerous PDL Fbs in the PDL remnant actively migrated into the coagulum and continued to proliferate. On the basis of the high proliferative activity and small number of cellular organelles responsible for procollagen synthesis, these cells appear immature. At 3 days, Fbs contained more cellular organelles and deposited more collagen fibers as they replaced the coagulum with dense connective tissue and the LI declined. At 4 and 5 days, some of the Fbs began to differentiate into Obs, and the proliferation of Fbs dramatically decreased to baseline values. The migration of PDL Fbs and their differentiation into Obs were investigated by labeling with 3H-thymidine or BrdU 1 day after tooth extraction. Heavily labeled Fbs were observed in the PDL remnant at 1 day, in the coagulum at 2 days, and in the dense connective tissue at 3 days. Labeled Obs associated with new bone were seen 4 days after injection. Endosteal and paravascular Fbs also proliferated, but at a lower level and at later time periods than the PDL Fbs. Surprisingly, endosteal and paravascular Fbs contributed only a small population of Fbs to socket healing.
These results indicate that PDL Fbs after tooth extraction actively proliferative, migrate into the coagulum, form dense connective tissue, and differentiate into Obs which form new bone during socket healing.
拔牙后的整个牙槽窝内充满了由成骨细胞形成的新骨,但这些成骨细胞的来源尚不清楚。因此,研究了大鼠上颌第一磨牙拔除后牙槽窝愈合过程中血管旁和成骨内膜成纤维细胞以及牙周膜成纤维细胞的增殖、迁移及其向成骨细胞的分化。
分别注射3H-胸腺嘧啶核苷和5-溴-2'-脱氧尿苷(BrdU)后,采用放射自显影术和免疫组织化学方法研究拔牙后牙槽窝内这些细胞的增殖活性和迁移情况。通过透射电子显微镜观察它们在分化过程中的形态变化。
拔牙后1天,牙周膜成纤维细胞是牙槽窝牙周膜残余中的主要细胞类型。拔牙后16小时内增殖率较低(标记指数(LI)约为2%),但拔牙后1天急剧增加至最高水平(LI = 23%)。在1至2天之间,牙周膜残余中的大量牙周膜成纤维细胞积极迁移到血凝块中并继续增殖。基于其高增殖活性和负责前胶原合成的细胞器数量较少,这些细胞显得不成熟。3天时,成纤维细胞含有更多的细胞器,并沉积了更多的胶原纤维,此时它们用致密结缔组织取代了血凝块,标记指数下降。4天和5天时,一些成纤维细胞开始分化为成骨细胞,成纤维细胞的增殖急剧下降至基线值。拔牙后1天用3H-胸腺嘧啶核苷或BrdU标记研究牙周膜成纤维细胞的迁移及其向成骨细胞的分化。1天时在牙周膜残余中观察到大量标记的成纤维细胞,2天时在血凝块中,3天时在致密结缔组织中。注射后4天可见与新骨相关的标记成骨细胞。骨内膜和成血管成纤维细胞也有增殖,但比牙周膜成纤维细胞增殖水平低且时间晚。令人惊讶的是,骨内膜和成血管成纤维细胞对牙槽窝愈合的成纤维细胞群体贡献很小。
这些结果表明,拔牙后牙周膜成纤维细胞积极增殖,迁移到血凝块中,形成致密结缔组织,并分化为成骨细胞,后者在牙槽窝愈合过程中形成新骨。