Narayanan A S, Ikezawa K, Wu D, Pitaru S
Department of Pathology, University of Washington, Seattle 98195, USA.
Connect Tissue Res. 1995;33(1-3):19-21. doi: 10.3109/03008209509016976.
We have isolated two polypeptides from cementum one of which promotes the growth and the other the attachment of periodontal cells. One polypeptide, the cementum derived growth factor (CGF), was extracted from healthy human and bovine teeth by 1 M CH3COOH and purified by heparin-affinity chromatography and HPLC. The CGF is a 23 kDa polypeptide which is mitogenic to fibroblasts and smooth muscle cells. It is active alone, but its activity is highly potentiated by plasma-derived serum or EGF. It induces classical mitogenic signaling events, which include Ca++ mobilization, inositol phosphate hydrolysis, activation of phosphokinase C (PKC) and transcription of cellular protooncogenes c-fos and jun-B. The magnitude and pattern of activation of signaling events and their susceptibility to PKC inhibitors and pertussis toxin indicated that the CGF may be a distinct molecular species. The CAP is a 55 kDa polypeptide which promotes the attachment and spreading of fibroblasts, smooth muscle cells, bone cells and endothelial cells, but not epithelial cells. Antibodies to CAP immunostain cementum, but not other tissues. Root surfaces bind CAP. The CGF and CAP do not appear to be present in adjacent periodontal structures. Our data show that the CAP and CGF selectively interact with periodontal cell populations and affect their biological activities, and thus may influence the formation and regeneration of periodontal connective tissues.
我们从牙骨质中分离出了两种多肽,其中一种促进牙周细胞的生长,另一种促进牙周细胞的附着。一种多肽,即牙骨质衍生生长因子(CGF),通过1M CH3COOH从健康人牙和牛牙中提取,并经肝素亲和层析和高效液相色谱法纯化。CGF是一种23kDa的多肽,对成纤维细胞和平滑肌细胞具有促有丝分裂作用。它单独具有活性,但其活性可被血浆来源血清或表皮生长因子(EGF)显著增强。它诱导经典的有丝分裂信号事件,包括钙离子动员、肌醇磷酸水解、磷酸激酶C(PKC)激活以及细胞原癌基因c-fos和jun-B的转录。信号事件激活的程度和模式及其对PKC抑制剂和百日咳毒素的敏感性表明,CGF可能是一种独特的分子类型。CAP是一种55kDa的多肽,它促进成纤维细胞、平滑肌细胞、骨细胞和内皮细胞的附着和铺展,但不促进上皮细胞的附着和铺展。针对CAP的抗体对牙骨质进行免疫染色,但对其他组织不进行免疫染色。牙根表面结合CAP。CGF和CAP似乎不存在于相邻的牙周结构中。我们的数据表明,CAP和CGF与牙周细胞群体选择性相互作用并影响其生物学活性,因此可能影响牙周结缔组织的形成和再生。