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易美齿健对大鼠牙周创伤后细胞分化的调控作用

Emdogain regulation of cellular differentiation in wounded rat periodontium.

作者信息

Chano Laura, Tenenbaum Howard C, Lekic P Charles, Sodek Jaro, McCulloch Christopher A

机构信息

CIHR Group in Matrix Dynamics, Faculty of Dentistry, University of Toronto, Canada.

出版信息

J Periodontal Res. 2003 Apr;38(2):164-74. doi: 10.1034/j.1600-0765.2003.00003.x.

Abstract

Emdogain is an enamel matrix derivative that may promote periodontal regeneration by recapitulating critical events in tooth morphogenesis. We hypothesized that Emdogain enhances periodontal regeneration by promoting the differentiation of cells required for the synthesis of periodontal ligament, bone and cementum. Cell differentiation was examined in rat periodontal window wounds in which there is no microbial biofilm or epithelial downgrowth, thereby simplifying the model system. Defects were filled with vehicle control or Emdogain (3 mg/ml or 30 mg/ml). Rats were sacrificed at 7, 14 and 21 d after wounding. Specimens of periodontium were immunostained for osteopontin, bone sialoprotein, osteocalcin as markers of osteogenic differentiation and for alpha-smooth muscle actin, a myofibroblastic marker. Morphometry and 3H-proline radioautography were used for assessment of tissue homeostasis and matrix production. Rats treated with Emdogain (only at 30 mg/ml) showed widening of the periodontal ligament at 7 d; by 14 and 21 d, periodontal ligament width was restored to normal values for all groups. Emdogain exerted no effect on cementum thickness, bone volume, osteoid deposition rates, or extracellular staining for osteopontin, bone sialoprotein or osteocalcin. Further, the percentage of cells with intracellular staining for osteopontin, osteocalcin or bone sialoprotein was unaffected by Emdogain. Staining for alpha-smooth muscle actin was abundant in the repopulating wound but was also unaffected by Emdogain. In conclusion, Emdogain does not apparently affect the expression of differentiation markers or bone matrix protein synthesis in the repopulation response of wounded rat molar periodontium. Therefore the effect of Emdogain on wound healing in the periodontium may be independent of differentiation in the cell populations examined in this model.

摘要

Emdogain是一种釉基质衍生物,它可能通过重现牙齿形态发生过程中的关键事件来促进牙周组织再生。我们假设Emdogain通过促进合成牙周膜、骨和牙骨质所需细胞的分化来增强牙周组织再生。在大鼠牙周窗伤口中检测细胞分化,该伤口不存在微生物生物膜或上皮下移,从而简化了模型系统。缺损处填充载体对照或Emdogain(3mg/ml或30mg/ml)。在受伤后7、14和21天处死大鼠。对牙周组织标本进行免疫染色,检测骨桥蛋白、骨涎蛋白、骨钙素作为成骨分化标志物,以及α-平滑肌肌动蛋白作为肌成纤维细胞标志物。形态计量学和3H-脯氨酸放射自显影用于评估组织稳态和基质产生。用Emdogain治疗的大鼠(仅30mg/ml组)在7天时牙周膜增宽;到14天和21天时,所有组的牙周膜宽度恢复到正常值。Emdogain对牙骨质厚度、骨体积、类骨质沉积率或骨桥蛋白、骨涎蛋白或骨钙素的细胞外染色没有影响。此外,骨桥蛋白、骨钙素或骨涎蛋白细胞内染色的细胞百分比不受Emdogain影响。α-平滑肌肌动蛋白染色在再填充的伤口中丰富,但也不受Emdogain影响。总之,Emdogain在受伤大鼠磨牙牙周组织的再填充反应中似乎不影响分化标志物的表达或骨基质蛋白合成。因此,Emdogain对牙周组织伤口愈合的影响可能独立于该模型中所检测细胞群体的分化。

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