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白细胞介素-10在体内外均是一种系膜细胞生长因子。

Interleukin-10 is a mesangial cell growth factor in vitro and in vivo.

作者信息

Chadban S J, Tesch G H, Foti R, Atkins R C, Nikolic-Paterson D J

机构信息

Department of Nephrology, Monash Medical Centre, Clayton, Victoria, Australia.

出版信息

Lab Invest. 1997 May;76(5):619-27.

PMID:9166281
Abstract

Macrophages are involved in the pathogenesis of mesangioproliferative glomerulonephritis. As macrophages are known to produce interleukin-10 (IL-10), we investigated the effect of recombinant murine IL-10 (rIL-10) on mesangial cell growth. In vitro studies were performed using the rat 1097 mesangial cell line. These cells exhibited a dose-dependent proliferative response to rIL-10 (23% to 70% increases at 80 ng/mL; p < 0.01), as assessed by both 3H-thymidine uptake and cell count. This effect was inhibited by preincubation of rIL-10 with a neutralizing anti-IL-10 antibody. When added to cultures of growth-arrested 1097 cells, IL-10 induced dose-dependent proliferation that paralleled the effects of platelet-derived growth factor. Incubation with a neutralizing anti-IL-10 Ab for 48 hours reduced 3H-thymidine uptake (median, 27% decreases; range, 2% to 56% decreases) versus a control Ab; p < 0.05). Rat mesangial cells were also shown to express IL-10 mRNA and protein, as determined by Northern blotting and immunostaining, thereby suggesting a role for IL-10 in autocrine mesangial cell growth. To examine the effects of IL-10 in vivo, inbred male Sprague-Dawley rats were given subcutaneous rIL-10 (0.5 mg/kg) for 3 (n = 6), 7 (n = 3), or 14 days (n = 4), or vehicle control, then killed. IL-10 administration induced a transient reduction in creatinine clearance of 35% at Day 3 (p < 0.01). Following IL-10 administration, an increase in glomerular cellularity was seen, which was maximal at Day 3 (82.7 +/- 5.9 nuclei/glomerular cross section versus control 64.6 +/- 4.6, 28% increases; p < 0.001) and maintained at Day 14 (23% increases; p < 0.01). Immuno-histochemical staining for proliferating cell nuclear antigen demonstrated an increased number of proliferating cells per glomerular cross section at day 3 (48% increases versus controls; p < 0.05). Staining for alpha-smooth-muscle actin showed significant labeling only in the glomeruli of IL-10-treated animals; double-labeling with an anti-proliferating cell nuclear antigen Ab demonstrated that some of these mesangial cells were proliferating. Collectively, these results suggest that IL-10 is a growth factor for rat mesangial cells both in vitro and in vivo.

摘要

巨噬细胞参与系膜增生性肾小球肾炎的发病机制。由于已知巨噬细胞可产生白细胞介素-10(IL-10),我们研究了重组鼠IL-10(rIL-10)对系膜细胞生长的影响。使用大鼠1097系膜细胞系进行体外研究。通过3H-胸腺嘧啶核苷摄取和细胞计数评估,这些细胞对rIL-10表现出剂量依赖性增殖反应(80 ng/mL时增加23%至70%;p<0.01)。用中和性抗IL-10抗体预孵育rIL-10可抑制这种效应。当添加到生长停滞的1097细胞培养物中时,IL-10诱导剂量依赖性增殖,这与血小板衍生生长因子的作用相似。与中和性抗IL-10抗体孵育48小时可使3H-胸腺嘧啶核苷摄取减少(中位数减少27%;范围为2%至56%减少),与对照抗体相比,p<0.05)。通过Northern印迹和免疫染色确定,大鼠系膜细胞也表达IL-10 mRNA和蛋白,从而提示IL-10在系膜细胞自分泌生长中起作用。为了研究IL-10在体内的作用,将近交系雄性Sprague-Dawley大鼠皮下注射rIL-10(0.5 mg/kg),持续3天(n = 6)、7天(n = 3)或14天(n = 4),或注射载体对照,然后处死。给予IL-10后,第3天肌酐清除率短暂降低35%(p<0.01)。给予IL-10后,可见肾小球细胞增多,在第3天达到最大值(82.7±5.9个核/肾小球横截面,对照为64.6±4.6,增加28%;p<0.001),并在第14天维持(增加23%;p<0.01)。增殖细胞核抗原的免疫组织化学染色显示,第3天每个肾小球横截面增殖细胞数量增加(比对照增加48%;p<0.05)。α-平滑肌肌动蛋白染色仅在接受IL-10治疗的动物的肾小球中显示出显著标记;用抗增殖细胞核抗原抗体进行双重标记表明,这些系膜细胞中的一些正在增殖。总体而言,这些结果表明IL-10在体外和体内都是大鼠系膜细胞的生长因子。

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