Sindet-Pedersen S, Gram J, Jespersen J
Department of Oral and Maxillofacial Surgery, Arhus University Hospital, Denmark.
J Dent Res. 1990 Jun;69(6):1283-6. doi: 10.1177/00220345900690061201.
We studied the fibrinolytic activities of the following subfractions of unstimulated human whole saliva on plasminogen-rich fibrin plates: (1) submandibular saliva, (2) parotid saliva, and (3) smears of buccal epithelial cells from ten healthy males. A cell-bound plasminogen activator could be demonstrated in the sediments of all three subfractions of whole saliva. The incorporation of antibodies (goat IgG) against human two-chain tissue-type plasminogen activator (t-PA) could quench the assessed fibrinolytic activities, whereas additional experiments suggested the absence of urokinase-like and F XII-dependent activators of fibrinolysis. The determinations in growth medium from buccal-epithelial cell culture of t-PA antigen by means of enzyme-linked immunosorbent assay showed the presence of t-PA. These clinical and experimental findings suggest that buccal-epithelial cells produce t-PA, while the activity of t-PA in parotid and submandibular saliva is very low.
(1)下颌下唾液,(2)腮腺唾液,以及(3)来自十名健康男性的颊上皮细胞涂片。在全唾液的所有三个亚组分的沉淀物中均可证实存在一种细胞结合的纤溶酶原激活剂。加入针对人双链组织型纤溶酶原激活剂(t-PA)的抗体(山羊IgG)可抑制所评估的纤溶活性,而进一步的实验表明不存在尿激酶样和F XII依赖性纤溶激活剂。通过酶联免疫吸附测定法对颊上皮细胞培养物的生长培养基中的t-PA抗原进行测定,结果显示存在t-PA。这些临床和实验结果表明,颊上皮细胞产生t-PA,而腮腺和下颌下唾液中t-PA的活性非常低。