Dynamic profiling of intra- and extra-cellular L/D-amino acids metabolism in colorectal cell and intestinal epithelial cell.

IF 3.1 3区 医学 Q2 CHEMISTRY, ANALYTICAL Journal of pharmaceutical and biomedical analysis Pub Date : 2025-03-15 Epub Date: 2024-12-09 DOI:10.1016/j.jpba.2024.116622
Wenchan Deng, Rongrong Huang, Yuanjiang Pan, Cuirong Sun
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Abstract

The metabolism process of amino acids is closely related to the growth of normal and cancer cells. It is still not clear how L/D-configuration amino acids participate in the metabolism of colorectal cell. Herein, intra- and extra-cellular metabolic distribution of L/D-amino acids in colorectal cell (HCT116) and human normal intestinal epithelial cell (NCM460) were profiled utilizing HPLC-MS/MS coupled with a chiral probe. The results displayed the differential metabolic portrayal for the two cell lines. Compared with NCM460 cell, 13 kinds of significant differential amino acids were founded in a lower concentration within HCT116 cell, and L-Gln was even not detected for intra-cell; as for extra-cell culture medium, the HCT116 cell consumed more L-Gln, D-Phe and D-Leu, while L-Met was low ingested in HCT116 cell. L-Ala and Gly were excretion in both two cell lines, excepted L-Cit which was uptake in HCT116 and excretion in NCM460 cell. Furthermore, the dynamic changes of chiral amino acids displayed that phenylalanine, tyrosine and tryptophan biosynthesis and arginine biosynthesis is the major pathway for intra-cellular metabolites and extra-cellular metabolites, respectively. Moreover, with additional D-amino acids in culture medium, the results exhibited that high concentration of D-amino acids have no significant effect on the proliferation of NCM460 cell, but could influence the profiling of amino acids metabolites, and further affect the proliferation of HCT116 cell. This present work enhances the understanding of these differential amino acids metabolic network and depicts a dynamic process of metabolic dysregulation of HCT116 and NCM460 cell.

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结直肠细胞和肠上皮细胞细胞内和细胞外L/ d氨基酸代谢的动态分析。
氨基酸的代谢过程与正常细胞和癌细胞的生长密切相关。L/ d构型氨基酸如何参与结直肠细胞的代谢尚不清楚。本研究利用HPLC-MS/MS结合手性探针分析了L/ d氨基酸在结直肠细胞(HCT116)和人正常肠上皮细胞(NCM460)细胞内和细胞外的代谢分布。结果显示了两种细胞系的差异代谢写照。与NCM460细胞相比,HCT116细胞内存在13种显著差异的氨基酸,且浓度较低,细胞内甚至未检测到L-Gln;细胞外培养基中,HCT116细胞摄取L-Gln、D-Phe和D-Leu较多,L-Met摄取较少。除了L-Cit在HCT116中被摄取,在NCM460细胞中被排泄外,L-Ala和Gly在两种细胞系中均被排泄。此外,手性氨基酸的动态变化表明,苯丙氨酸、酪氨酸和色氨酸的生物合成和精氨酸的生物合成分别是细胞内代谢物和细胞外代谢物的主要途径。此外,在培养基中添加d -氨基酸,结果表明高浓度d -氨基酸对NCM460细胞的增殖没有显著影响,但会影响氨基酸代谢物的谱,进而影响HCT116细胞的增殖。本研究增强了对这些差异氨基酸代谢网络的认识,并描绘了HCT116和NCM460细胞代谢失调的动态过程。
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文献相关原料
公司名称
产品信息
索莱宝
penicillin-streptomycin
索莱宝
penicillin-streptomycin
阿拉丁
alanine
阿拉丁
isoleucine (Ile)
阿拉丁
leucine (Leu)
阿拉丁
methionine
阿拉丁
phenylalanine (Phe)
阿拉丁
serine
阿拉丁
threonine (Thr)
阿拉丁
tryptophan (Trp)
阿拉丁
tyrosine (Tyr)
阿拉丁
valine (Val)
阿拉丁
glycine
来源期刊
CiteScore
6.70
自引率
5.90%
发文量
588
审稿时长
37 days
期刊介绍: This journal is an international medium directed towards the needs of academic, clinical, government and industrial analysis by publishing original research reports and critical reviews on pharmaceutical and biomedical analysis. It covers the interdisciplinary aspects of analysis in the pharmaceutical, biomedical and clinical sciences, including developments in analytical methodology, instrumentation, computation and interpretation. Submissions on novel applications focusing on drug purity and stability studies, pharmacokinetics, therapeutic monitoring, metabolic profiling; drug-related aspects of analytical biochemistry and forensic toxicology; quality assurance in the pharmaceutical industry are also welcome. Studies from areas of well established and poorly selective methods, such as UV-VIS spectrophotometry (including derivative and multi-wavelength measurements), basic electroanalytical (potentiometric, polarographic and voltammetric) methods, fluorimetry, flow-injection analysis, etc. are accepted for publication in exceptional cases only, if a unique and substantial advantage over presently known systems is demonstrated. The same applies to the assay of simple drug formulations by any kind of methods and the determination of drugs in biological samples based merely on spiked samples. Drug purity/stability studies should contain information on the structure elucidation of the impurities/degradants.
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