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首页> 外文期刊>Nephron >A distinct population of tubular cells in the distal S3 segment contributes to S3 segment regeneration in rats following acute renal failure induced by uranyl acetate.
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A distinct population of tubular cells in the distal S3 segment contributes to S3 segment regeneration in rats following acute renal failure induced by uranyl acetate.

机译:在由乙酸铀酰引起的急性肾衰竭后,远端S3节段中不同的肾小管细胞群有助于大鼠S3节段的再生。

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BACKGROUND: We previously reported that early regenerating cells found at the distal area of the S3 segment of the nephron (designated as target cells) were label-retaining cells in uranyl acetate (UA)-induced acute renal failure (ARF) in rats. In this study, we examined the contribution of these target cells to S3 segment repair after UA treatment. We also discriminated target cells from bromodeoxyuridine (BrdU)-label-retaining cells labeled under normal conditions and examined their capacity to proliferate following a second insult and their resistance to 5-fluorouracil (5-FU). METHODS: Target cells were labeled and tracked using a (3)H-thymidine pulse/chase approach after UA (4 mg/kg) injection to rats. Normal rats were labeled with BrdU, and cells positive for BrdU and Ki67 were analyzed after UA treatment. The kinetics of target cells was examined after a second dose of UA and treatment with 5-FU. RESULTS: The target cells were strongly labeled by (3)H-thymidine and were predominantly found in the distal quarter of the S3 segment until 40 weeks after generating 'label-diluted' cells throughout the S3 segment. Cells labeled with BrdU under normal conditions did not express Ki67 after UA treatment but target cells were Ki67-positive. The target cells underwent further proliferation following the second treatment with UA and were transiently arrested by 5-FU treatment at G0/G1 after UA. CONCLUSIONS: The target cells are slow-cycling cells, resistant to 5-FU treatment and have the capacity to undergo further proliferation following a second insult with UA. These data suggest the presence of a distinct population of cells that can regenerate the S3 segment in UA-induced ARF.
机译:背景:我们以前曾报道,在肾单位S3段远端区域发现的早期再生细胞(称为靶细胞)是醋酸铀酰(UA)诱导的大鼠急性肾衰竭(ARF)中的标记保留细胞。在这项研究中,我们检查了这些靶细胞在UA治疗后对S3段修复的贡献。我们还从正常条件下标记的溴脱氧尿苷(BrdU)-标记保留细胞中区分了靶细胞,并检查了第二次感染后它们的增殖能力以及它们对5-氟尿嘧啶(5-FU)的抗性。方法:对大鼠注射UA(4 mg / kg)后,用(3)H-胸苷脉冲/追踪法标记和追踪靶细胞。正常大鼠用BrdU标记,UA处理后分析BrdU和Ki67阳性的细胞。在第二次服用UA并用5-FU处理后,检查了靶细胞的动力学。结果:目标细胞被(3)H-胸腺嘧啶核苷强烈标记,主要在S3区段的远端四分之一处发现,直到在整个S3区段产生“标记稀释的”细胞后40周。 UA处理后,正常条件下用BrdU标记的细胞不表达Ki67,但靶细胞为Ki67阳性。在用UA进行第二次处理后,靶细胞进一步增殖,并在UA后通过G0 / G1处的5-FU处理被瞬时阻滞。结论:靶细胞是慢循环细胞,对5-FU治疗有抗性,并具有在再次受到UA侵害后能够进一步增殖的能力。这些数据表明存在可以在UA诱导的ARF中再生S3区段的独特细胞群。

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