小鼠肾脏中的 TRPM6--目标和抗体。

IF 3.1 4区 医学 Q2 PHARMACOLOGY & PHARMACY Naunyn-Schmiedeberg's archives of pharmacology Pub Date : 2025-08-01 Epub Date: 2025-03-01 DOI:10.1007/s00210-025-03951-0
Colya N Englisch, Coline M Diebolt, Emilie Kirstein, Vanessa Wahl, Philipp Wartenberg, Dirk Schaudien, Anja Beckmann, Matthias W Laschke, Gabriela Krasteva-Christ, Thomas Gudermann, Vladimir Chubanov, Ulrich Boehm, Thomas Tschernig
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引用次数: 0

摘要

镁是人体中含量第四丰富的阳离子。作为许多酶促反应的关键参与者,镁稳态失衡会导致严重的疾病。在21世纪初,瞬时受体电位美拉他汀通道6 (TRPM6)被确定为肾远曲小管(DCT) Mg2+重吸收的关键蛋白。肾脏是一个高度动态的系统,是负责盐/水适应环境变化的关键界面。因此,如前所述,肾脏TRPM6表达和Mg2+重吸收可能不局限于DCT。为了解决这个问题,蛋白质靶向是强制性的,因为基因组检测不足以得出功能性表达的结论。为此,我们使用了来自成熟制造商的多克隆TRPM6抗体,并检测了小鼠近端和远端小管的免疫染色。事实上,大多数市售TRPM6抗体的特异性都没有得到充分的验证,这依赖于缺乏组成性TRPM6敲除。因此,我们使用条件trpm6基因敲除小鼠进行对照实验。与使用TRPM6抗体的野生型相比,在敲除组织中观察到类似的信号。与TRPM7表位或其他多肽重叠是可能的。因此,TRPM6免疫组织化学和免疫荧光结果难以解释,肾脏TRPM6表达谱尚未阐明。
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TRPM6 in murine kidneys-of targets and antibodies.

Magnesium is the fourth most abundant cation in the human organism. As a key-player in many enzymatic reactions, magnesium homeostasis disbalance can cause severe disorders. In the early 2000s, the transient receptor potential melastatin channel 6 (TRPM6) was identified as a critical protein in renal Mg2+-reabsorption in the distal convoluted tubule (DCT). As the key-interface responsible for salt/water adaptation to environmental changes, the kidney is a highly dynamic system. Therefore, renal TRPM6 expression and Mg2+-reabsorption might not be restricted to the DCT, as previously indicated. To address this, protein targeting is mandatory since genomic detection is insufficient to conclude on functional expression. For this purpose, we used a polyclonal TRPM6 antibody from an established manufacturer and detected immunostaining in murine proximal and distal tubules. As a matter of fact, the specificity of most commercially available TRPM6 antibodies is insufficiently validated which relies on the lack of constitutive trpm6 knockouts. Therefore, conditional trpm6 knockout mice were used for control experiments. Similar signals were observed in the knockout tissue when compared to wildtype using the TRPM6 antibody. Overlaps with TRPM7 epitopes or other peptides are conceivable. Thus, TRPM6 immunohistochemistry and immunofluorescence results are difficult to interpret, and the spectrum of renal TRPM6 expression is not yet elucidated.

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来源期刊
CiteScore
6.20
自引率
5.60%
发文量
142
审稿时长
4-8 weeks
期刊介绍: Naunyn-Schmiedeberg''s Archives of Pharmacology was founded in 1873 by B. Naunyn, O. Schmiedeberg and E. Klebs as Archiv für experimentelle Pathologie und Pharmakologie, is the offical journal of the German Society of Experimental and Clinical Pharmacology and Toxicology (Deutsche Gesellschaft für experimentelle und klinische Pharmakologie und Toxikologie, DGPT) and the Sphingolipid Club. The journal publishes invited reviews, original articles, short communications and meeting reports and appears monthly. Naunyn-Schmiedeberg''s Archives of Pharmacology welcomes manuscripts for consideration of publication that report new and significant information on drug action and toxicity of chemical compounds. Thus, its scope covers all fields of experimental and clinical pharmacology as well as toxicology and includes studies in the fields of neuropharmacology and cardiovascular pharmacology as well as those describing drug actions at the cellular, biochemical and molecular levels. Moreover, submission of clinical trials with healthy volunteers or patients is encouraged. Short communications provide a means for rapid publication of significant findings of current interest that represent a conceptual advance in the field.
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