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