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普雷丁的最后一程。

The final walk with preptin.

机构信息

Institute of Organic Chemistry and Biochemistry of the Czech Academy of Sciences, Prague, Czech Republic.

Faculty of Science, Department of Cell Biology, Charles University, Prague, Czech Republic.

出版信息

PLoS One. 2024 Sep 12;19(9):e0309726. doi: 10.1371/journal.pone.0309726. eCollection 2024.

DOI:10.1371/journal.pone.0309726
PMID:39264940
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11392399/
Abstract

Preptin, a 34-amino acid peptide derived from pro-IGF2, is believed to influence various physiological processes, including insulin secretion and the regulation of bone metabolism. Despite its recognized involvement, the precise physiological role of preptin remains enigmatic. To address this knowledge gap, we synthesized 16 analogs of preptin, spanning a spectrum from full-length forms to fragments, and conducted comprehensive comparative activity evaluations alongside native human, mouse and rat preptin. Our study aimed to elucidate the physiological role of preptin. Contrary to previous indications of broad biological activity, our thorough analyses across diverse cell types revealed no significant biological activity associated with preptin or its analogs. This suggests that the associations of preptin with various diseases or tissue-specific abundance fluctuations may be influenced by factors beyond preptin itself, such as higher levels of IGF2 or IGF2 proforms present in tissues. In conclusion, our findings challenge the conventional notion of preptin as an isolated biologically active molecule and underscore the complexity of its interactions within biological systems. Rather than acting independently, the observed effects of preptin may arise from experimental conditions, elevated preptin concentrations, or interactions with related molecules such as IGF2.

摘要

前胃肽,一种源自 pro-IGF2 的 34 个氨基酸肽,被认为影响多种生理过程,包括胰岛素分泌和骨代谢的调节。尽管已经认识到其参与作用,但前胃肽的确切生理作用仍然神秘。为了填补这一知识空白,我们合成了 16 种前胃肽类似物,涵盖了全长形式到片段的范围,并对天然人、鼠和大鼠前胃肽进行了全面的比较活性评估。我们的研究旨在阐明前胃肽的生理作用。与之前广泛的生物学活性的指示相反,我们在不同细胞类型中的彻底分析没有发现与前胃肽或其类似物相关的显著生物学活性。这表明,前胃肽与各种疾病的关联或组织特异性丰度波动可能受到超出前胃肽本身的因素的影响,例如组织中存在更高水平的 IGF2 或 IGF2 前体。总之,我们的发现挑战了前胃肽作为一种孤立的具有生物活性的分子的传统观念,并强调了其在生物系统中的相互作用的复杂性。前胃肽的观察到的作用不是独立作用的,可能源于实验条件、前胃肽浓度升高,或与 IGF2 等相关分子的相互作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1290/11392399/979550984b1d/pone.0309726.g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1290/11392399/9052f1971ad0/pone.0309726.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1290/11392399/7b9f960a4b9e/pone.0309726.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1290/11392399/b61f880dbe83/pone.0309726.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1290/11392399/b17f2d68a089/pone.0309726.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1290/11392399/e73e5f945ff1/pone.0309726.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1290/11392399/585f4bd7a9c3/pone.0309726.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1290/11392399/32508394db8e/pone.0309726.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1290/11392399/642ac7205e51/pone.0309726.g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1290/11392399/979550984b1d/pone.0309726.g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1290/11392399/9052f1971ad0/pone.0309726.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1290/11392399/7b9f960a4b9e/pone.0309726.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1290/11392399/b61f880dbe83/pone.0309726.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1290/11392399/b17f2d68a089/pone.0309726.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1290/11392399/e73e5f945ff1/pone.0309726.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1290/11392399/585f4bd7a9c3/pone.0309726.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1290/11392399/32508394db8e/pone.0309726.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1290/11392399/642ac7205e51/pone.0309726.g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1290/11392399/979550984b1d/pone.0309726.g009.jpg

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Open Biol. 2023 Nov;13(11):230142. doi: 10.1098/rsob.230142. Epub 2023 Nov 8.
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Preptin Deficiency Does Not Protect against High-Fat Diet-Induced Metabolic Dysfunction or Bone Loss in Mice.前ptin缺乏不能预防小鼠高脂饮食诱导的代谢功能障碍或骨质流失。
JBMR Plus. 2023 Jun 18;7(8):e10777. doi: 10.1002/jbm4.10777. eCollection 2023 Aug.
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Non-glycosylated IGF2 prohormones are more mitogenic than native IGF2.
非糖基化 IGF2 前激素比天然 IGF2 更具有丝分裂活性。
Commun Biol. 2023 Aug 19;6(1):863. doi: 10.1038/s42003-023-05239-6.
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Genetic ablation of the preptin-coding portion of impairs pancreatic function in female mice.缺失 preptin 编码部分的基因会损害雌性小鼠的胰腺功能。
Am J Physiol Endocrinol Metab. 2022 Dec 1;323(6):E467-E479. doi: 10.1152/ajpendo.00401.2021. Epub 2022 Sep 21.
5
BeStSel: webserver for secondary structure and fold prediction for protein CD spectroscopy.BeStSel:用于蛋白质圆二色光谱二级结构和折叠预测的网络服务器。
Nucleic Acids Res. 2022 Jul 5;50(W1):W90-W98. doi: 10.1093/nar/gkac345.
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Functional stapled fragments of human preptin of minimised length.最小长度的人类前胰岛素功能订书钉片段。
Org Biomol Chem. 2022 Mar 23;20(12):2446-2454. doi: 10.1039/d1ob02193a.
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A radioligand receptor binding assay for measuring of insulin secreted by MIN6 cells after stimulation with glucose, arginine, ornithine, dopamine, and serotonin.用于测量葡萄糖、精氨酸、鸟氨酸、多巴胺和 5-羟色胺刺激 MIN6 细胞后胰岛素分泌的放射性配体受体结合测定法。
Anal Bioanal Chem. 2021 Jul;413(17):4531-4543. doi: 10.1007/s00216-021-03423-3. Epub 2021 May 29.
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