Chair and Division of Nephrology, University of Bari. Polyclinic, Piazza G. Cesare, 11, 70124, Bari, Italy.
Cytotechnology. 1993 Jan;11(Suppl 1):S103-5. doi: 10.1007/BF00746069.
Renal mesangial cell (MC) cultures are easily established and widely used. MC produce some complement (C) regulatory proteins. We studied whether MC synthesize C components (C3, C5, C8). MC cultures were established from normal portions of cortices of nephrectomies for renal cancer. After growing to near-confluence in RPMI/17% FBS and resting for 24 h in RPMI/0.5% FBS, MC were stimulated up to 72 h with IL-1β or IL-6 (10, 100, 1000 U/ml). Neither C5 nor C8 were detected by ELISA. While C3 was present in supernatant under basal conditions (15.5-107.6 ng/10(6) cells/24h) in different MC lines. IL-1β up-regulated the synthesis by 2.4-4.5 folds, whereas IL-6 did not show any effect. C3 synthetic rate was 1,76 ng/h/10(6) cells under IL-1 stimulation versus basal rate of 0,37 ng/h/10(6) cells. MC production of C3, especially induced by IL-1 may have pathogenetic relevance in glomerulonephritis.
肾系膜细胞(MC)培养易于建立且应用广泛。MC 可产生某些补体(C)调节蛋白。我们研究了 MC 是否合成 C 成分(C3、C5、C8)。从肾细胞癌肾切除术的正常皮质部分建立 MC 培养物。在 RPMI/17% FBS 中生长至接近汇合后,在 RPMI/0.5% FBS 中休息 24 小时,然后用 IL-1β 或 IL-6(10、100、1000 U/ml)刺激长达 72 小时。ELISA 未检测到 C5 或 C8。虽然在不同的 MC 系中,基础条件下(15.5-107.6 ng/10(6)细胞/24 小时)上清液中存在 C3。IL-1β 将合成率上调 2.4-4.5 倍,而 IL-6 没有任何作用。在 IL-1 刺激下,C3 的合成率为 1.76 ng/h/10(6)细胞,而基础率为 0.37 ng/h/10(6)细胞。MC 产生的 C3,特别是在 IL-1 诱导下,在肾小球肾炎中可能具有发病相关性。