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人工渗出液:血浆而非血清刺激细胞增殖与纤维蛋白溶解有关。

Artificial exudate: stimulation of cell proliferation by plasma not serum is associated with fibrinolysis.

作者信息

Stirk C M, Thompson W D

机构信息

Department of Pathology, Medical School, Aberdeen Royal Infirmary, UK.

出版信息

Blood Coagul Fibrinolysis. 1990 Oct;1(4-5):537-41.

PMID:2133231
Abstract

Despite its abundance of cell culture growth factors, serum does not enhance growth of the in vivo test system, the chick chorioallantoic membrane (CAM). Previously we have also shown that fibrinogen (Kabi) and its degradation products do not display mitogenic activity on the CAM, but have now been surprised to find stimulation of DNA synthesis (up to 2.5-fold) 18 h after application of human plasma [incorporation of [3H]thymidine control mean +/- SEM 8442 +/- 1338 dpm/CAM (n = 8); test--20 199 = 3491 (n = 6); t-test P less than 0.01)]. Plasma (platelet-rich and platelet-poor) was freshly prepared by minicolumn removal of citrate at 16 degrees C; 0.3 ml aliquots of 10% human plasma were applied to the CAM and groups were fixed at various time intervals. Cross-sections were examined histologically, including immunoperoxidase studies with antihuman fibrinogen which does not cross react with chick fibrinogen, and autoradiography with [3H]thymidine. Initially, a layer of plasma was observed on the surface of the CAM. After 1 h a condensed fibrillar layer of fibrin was formed and was still present at 6 h. This was associated with increased [3H]thymidine labelling of the surface layer of the CAM. By 18 h the fibrin had disappeared, indicating that it had been lysed by the CAM, and widespread [3H]thymidine labelling was observed. No inflammatory cell infiltrate was apparent, but marked oedema developed. Oedema alone was observed in controls receiving serum or Dulbecco buffer. Both platelet-rich and platelet-free plasma gave stimulation of mitogenic activity, implying that platelet-derived growth factor is not involved in the stimulation of the CAM.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

尽管血清富含细胞培养生长因子,但它并不能促进体内测试系统——鸡胚绒毛尿囊膜(CAM)的生长。此前我们还表明,纤维蛋白原(卡比)及其降解产物对CAM没有促有丝分裂活性,但现在我们惊讶地发现,在应用人血浆18小时后,DNA合成受到刺激(高达2.5倍)[ [3H]胸苷掺入对照平均值±标准误为8442±1338 dpm/CAM(n = 8);测试组为20199 = 3491(n = 6);t检验P<0.01]。血浆(富含血小板和缺乏血小板的)在16℃下通过微型柱去除柠檬酸盐新鲜制备;将0.3 ml 10%的人血浆等分试样应用于CAM,并在不同时间间隔固定各组。进行组织学检查横截面,包括用与人纤维蛋白原不发生交叉反应的抗人纤维蛋白原进行免疫过氧化物酶研究,以及用[3H]胸苷进行放射自显影。最初,在CAM表面观察到一层血浆。1小时后形成了一层凝聚的纤维蛋白纤维层,在6小时时仍然存在。这与CAM表层[3H]胸苷标记增加有关。到18小时时,纤维蛋白消失,表明它已被CAM溶解,并观察到广泛的[3H]胸苷标记。没有明显的炎性细胞浸润,但出现了明显的水肿。在接受血清或杜尔贝科缓冲液的对照组中仅观察到水肿。富含血小板和无血小板的血浆均能刺激有丝分裂活性,这意味着血小板衍生生长因子不参与对CAM的刺激。(摘要截短于250字)

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