优化肾脏转运体免疫检测:样品制备过程中的冻融后果。

Hannah L Hartman-Houstman, Donna L Ralph, Jonathan W Nelson, Lawrence G Palmer, Jessica E Faulkner, Jennifer C Sullivan, Desmond M Moronge, Alicia A McDonough
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引用次数: 0

摘要

肾脏转运体(协同转运体、通道、claudins)介导体液和电解质的平衡,是激素和治疗调节剂的靶标。通过免疫印迹法使用抗体探针评估肾脏转运体的丰度是机理研究的重要工具。虽然期刊要求作者证明抗体的特异性,但对于肾脏样本的制备却没有一致的指导原则,导致免疫印迹结果在实验室之间存在差异。在本研究中,我们确定了样品制备的影响,特别是冻融(Froz)与新鲜处理(Fresh)肾脏(雌性和雄性大鼠和小鼠)对 15 种肾脏转运体免疫印迹信号检测的影响,以及蛋白酶抑制剂在均质化过程中的影响。在使用阿普罗宁、Na2EDTA、PMSF 和磷酸酶抑制剂匀浆的雌性 Sprague Dawley 大鼠肾脏中,大多数转运体的免疫检测信号在冷冻样本中比新鲜样本低约 50%。加入额外的抑制剂(罗氏 cOmpleteTM 蛋白酶抑制剂,"+")只能将转运体免疫印迹信号部分提高到接近新鲜样本的水平。在雄性 Sprague Dawley 大鼠中,尽管使用了额外的抑制剂,但 Froz+ 与 Fresh+ 相比,免疫印迹信号密度更低。在 C57BL/6 雄性小鼠中,来自近端肾小管转运体的免疫印迹信号在 Froz 和 Fresh 之间的差异约为 25-50%,而在 Froz+ 中则更大。与此相反,雌性小鼠在 Froz 中表现出选择性转运体信号降低,但额外的蛋白酶抑制剂并不能改善这种情况。因此,肾脏样本制备变量(包括冻融和蛋白酶抑制)对免疫印迹定量肾脏转运体丰度有很大的转运体特异性影响。这些发现强调了评估和报告样本制备方案对转运体回收率的影响以确保严谨性和可重复性的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Optimizing renal transporter immunodetection: consequences of freeze-thaw during sample preparation.

Renal transporters (cotransporters, channels, and claudins) mediate homeostasis of fluids and electrolytes and are targets of hormonal and therapeutic regulators. Assessing renal transporter abundance with antibody probes by immunoblotting is an essential tool for mechanistic studies. Although journals require authors to demonstrate antibody specificity, there are no consensus guidelines for kidney sample preparation leading to lab-to-lab variability in immunoblot results. In this study, we determined the impact of sample preparation, specifically freeze-thawed (Frozen) versus freshly processed (Fresh) kidneys (female and male rats and mice) on immunoblot signal detection of 15 renal transporters and the impact of protease inhibitors during homogenization. In female Sprague-Dawley rat kidneys homogenized with aprotinin, Na2EDTA, PMSF, and phosphatase inhibitors, immunodetection signals were ∼50% lower in Frozen versus Fresh samples for most transporters. Inclusion of additional inhibitors (Roche cOmplete Protease Inhibitor, "+") only partially increased transporter immunoblot signals to near Fresh levels. In male Sprague-Dawley rats, immunoblot signal density was lower in Frozen+ versus Fresh+ despite additional inhibitors. In C57BL/6 male mice, immunoblot signals from proximal tubule transporters were lower in Frozen versus Fresh by ∼25-50% and greater in Frozen+. In contrast, immunodetection signal was equivalent in female Frozen+ versus female Fresh+ for claudin 2, villin, AQP1, NKCC2, NCC, ENaCβ, ENaCɣ, claudin 7, AQP2, NKAα1, and NKAβ1. Thus, kidney sample preparation variables, including freeze-thaw and protease inhibition, have substantial transporter-specific effects on quantification of renal transporter abundance by immunoblot. These findings underscore the critical importance of assessing and reporting the impact of sample preparation protocols on transporter recovery to ensure robust rigor and reproducibility. NEW & NOTEWORTHY Freeze-thawing kidneys before homogenization is widely accepted in renal research. This study demonstrates that if kidneys are freeze-thawed just once before homogenization, immunoblot signals are reduced in a transporter-specific manner in rats and mice dependent on sex and that immunoblot signals can be partially recovered by adding additional protease inhibitors. These findings underscore the critical importance of assessing the impact of sample preparation, including freeze-thaw versus fresh, to ensure robust rigor and reproducibility.

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