Cowan D H, Graham J
J Lab Clin Med. 1983 Dec;102(6):973-86.
The effect of platelet lysate on the growth of colonies of human tumor cells was examined in vitro by using the human tumor stem cell assay. Lysates were prepared from freeze-thawed outdated platelets. Eighteen to 446 colonies (mean 85) grew from 211 of 299 tumors plated at a density of 5 X 10(5) cells/plate. The plating efficiency ranged from 0.001% to 0.35%. The viability of the cells plated ranged from 10% to 90%. Platelet lysate significantly enhanced (p less than 0.05) colony formation from cells from 99 (47%) of 211 patients. The number of colonies grown with lysate from these 99 tumors ranged from 36 to 580 (mean 152). The enhancement factor varied from 1.25 to 6.69. Platelet lysate significantly decreased colony formation (p less than 0.05) from cells from 27 (13%) of the 211 tumors and had no effect on 85 (40%). Maximum increases over control occurred after 6 days in 79 (94%) of 84 tumors and after 10 days in 5 (6%). The extent of enhancement by platelet lysate of tumor colony formation correlated with cell viability (r = 0.545, p less than 0.005). The growth-promoting activity for human tumors was nondialyzable, stable with heating at 56 degrees or 70 degrees C for 30 min and at 100 degrees C for 2.5 min, substantially inactivated by heating at 100 degrees C for 5 min, and totally inactivated by heating at 90 degrees C for 30 min. It was partially inactivated by trypsin and abolished by periodate oxidation. The results suggest that a proportion of tumors of epithelial and mesodermal origin are responsive in vitro to growth-promoting factor(s) derived from human platelets.
采用人肿瘤干细胞检测法在体外检测血小板裂解物对人肿瘤细胞集落生长的影响。裂解物由冻融的过期血小板制备而成。在以每平板5×10⁵个细胞的密度接种的299个肿瘤中,有211个长出了18至446个集落(平均85个)。接种效率在0.001%至0.35%之间。接种细胞的活力在10%至90%之间。血小板裂解物显著增强了211例患者中99例(47%)患者的细胞集落形成(p<0.05)。这99个肿瘤的裂解物培养出的集落数量在36至580个之间(平均152个)。增强因子在1.25至6.69之间。血小板裂解物显著降低了211个肿瘤中27个(13%)患者的细胞集落形成(p<0.05),对85个(40%)没有影响。84个肿瘤中的79个(94%)在6天后出现了相对于对照的最大增加,5个(6%)在10天后出现。血小板裂解物对肿瘤集落形成的增强程度与细胞活力相关(r = 0.545,p<0.005)。人肿瘤的生长促进活性不可透析,在56℃或70℃加热30分钟以及在100℃加热2.5分钟时稳定,在100℃加热5分钟时基本失活,在90℃加热30分钟时完全失活。它可被胰蛋白酶部分失活,被高碘酸盐氧化消除活性。结果表明,一部分上皮和中胚层来源的肿瘤在体外对源自人血小板的生长促进因子有反应。