Transepithelial Transport of Hemp Protein-Derived Bioactive Peptide Trp-Tyr-Thr (WYT) in Human Caco-2 Cell Monolayers
文献类型: 外文期刊
第一作者: Wei, Ping
作者: Wei, Ping;Ling, Dongning;Tang, Yayuan;Deng, Zhonglin;Wei, Zhen;Wei, Ping;Ling, Dongning;Tang, Yayuan;Liu, Guoming;Liu, Guoming
作者机构:
关键词: Hemp; Bioactive peptide; Caco-2 cell monolayers; Transepithelial transport; Permeability
期刊名称:INTERNATIONAL JOURNAL OF PEPTIDE RESEARCH AND THERAPEUTICS ( 影响因子:2.4; 五年影响因子:2.0 )
ISSN: 1573-3149
年卷期: 2025 年 31 卷 4 期
页码:
收录情况: SCI
摘要: PurposeTo improve bioactive peptide absorption and bioavailability, in-depth understanding of their transport across the intestinal epithelium is crucial. In this study, we used Caco-2 cell monolayers to investigate the transepithelial transport of Trp-Tyr-Thr (WYT), a novel hemp protein-derived Angiotensin-I converting enzyme (ACE) peptide.MethodsFirstly, Caco-2 cell monolayer model was established and then various cell modulators (Gly-Pro, sodium azide, wortmannin and cytochalasin D) were used to study WYT transport.ResultsOur results demonstrated that WYT maintained its stability for more than 2 days and 2 h in Hank's balanced salt solution and on the apical surface of Caco-2 cells, respectively. WYT was transported intact across Caco-2 cell monolayers with an apparent permeability coefficient (Papp) of 1.03 x 10-7 cm/s. Our transport route evaluation revealed that Gly-Pro, a peptide transporter 1 (PepT1) substrate, significantly affected transepithelial permeability, suggesting that it mediated WYT transport across Caco-2 cell monolayers. Moreover, the ATPase inhibitor sodium azide significantly reduced the Papp of WYT, while the tight junction disruptor cytochalasin D and the transcytosis inhibitor wortmannin did not significantly affect WYT permeability.ConclusionIn summary, the results of our study indicate that WYT transport across Caco-2 cell monolayers occurs energy-dependently via the PepT1 pathway. It contributes to the study of hemp protein-derived bioactive peptide in lowering blood pressure and supports the development of bioactive peptide products.
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