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有机阳离子转运体1(OCTN1)介导A549肺癌细胞中的乙酰胆碱转运:可能的病理生理学意义。

OCTN1 mediates acetylcholine transport in the A549 lung cancer cells: possible pathophysiological implications.

作者信息

Pochini Lorena, Tedesco Giusi Elisabetta, Mazza Tiziano, Scalise Mariafrancesca, Indiveri Cesare

机构信息

Laboratory of Biochemistry, Molecular Biotechnology and Molecular Biology, Department DiBEST (Biologia, Ecologia, Scienze Della Terra), University of Calabria, Arcavacata di Rende, Italy.

Institute of Biomembranes, Bioenergetics and Molecular Biotechnologies (IBIOM), National Research Council (CNR), Bari, Italy.

出版信息

Front Mol Biosci. 2024 Dec 9;11:1512530. doi: 10.3389/fmolb.2024.1512530. eCollection 2024.


DOI:10.3389/fmolb.2024.1512530
PMID:39719963
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11666908/
Abstract

A role for acetylcholine in cell proliferation, epithelial mesenchymal transition and invasion has been well assessed and related to the presence of the non-neuronal cholinergic system in lung cancer. For the operation of this non-neuronal system, acetylcholine should be released by a transporter mediated non-quantal process. OCTN1 is one of the transporters able to catalyse acetylcholine efflux and . Using the A549 cell line as a lung cancer model, it has been found that these cells express OCTN1 at a higher level with respect to other cancer cells. The transport capacity of OCTN1 extracted from A549 and reconstituted into proteoliposomes reflects the protein expression profile. The properties of the acetylcholine transport mediated by OCTN1 of A549 in terms of specificity to ligands and ability to catalyse efflux of acetylcholine correspond to those previously described for the same transporter in other cells or to those of the human recombinant protein. OCTN1 is the major player in acetylcholine release in A549 and, therefore, may represent a target for inhibitors able to block the acetylcholine action in this type of aggressive tumors.

摘要

乙酰胆碱在细胞增殖、上皮-间质转化和侵袭中的作用已得到充分评估,且与肺癌中非神经元胆碱能系统的存在有关。对于该非神经元系统的运作,乙酰胆碱应以转运体介导的非量子过程释放。OCTN1是能够催化乙酰胆碱外排的转运体之一。以A549细胞系作为肺癌模型,研究发现,与其他癌细胞相比,这些细胞中OCTN1的表达水平更高。从A549中提取并重组到蛋白脂质体中的OCTN1的转运能力反映了蛋白质表达谱。A549的OCTN1介导的乙酰胆碱转运在对配体的特异性和催化乙酰胆碱外排的能力方面的特性,与先前在其他细胞中描述的同一转运体的特性或人重组蛋白的特性相符。OCTN1是A549中乙酰胆碱释放的主要参与者,因此,它可能是能够阻断这类侵袭性肿瘤中乙酰胆碱作用的抑制剂的作用靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8567/11666908/6515d7bd1379/fmolb-11-1512530-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8567/11666908/58bfd2111729/fmolb-11-1512530-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8567/11666908/1e507178e4de/fmolb-11-1512530-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8567/11666908/c84de5fbb779/fmolb-11-1512530-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8567/11666908/6515d7bd1379/fmolb-11-1512530-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8567/11666908/58bfd2111729/fmolb-11-1512530-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8567/11666908/1e507178e4de/fmolb-11-1512530-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8567/11666908/c84de5fbb779/fmolb-11-1512530-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8567/11666908/6515d7bd1379/fmolb-11-1512530-g004.jpg

相似文献

[1]
OCTN1 mediates acetylcholine transport in the A549 lung cancer cells: possible pathophysiological implications.

Front Mol Biosci. 2024-12-9

[2]
Immuno-detection of OCTN1 (SLC22A4) in HeLa cells and characterization of transport function.

Int Immunopharmacol. 2015-11

[3]
Acetylcholine and acetylcarnitine transport in peritoneum: Role of the SLC22A4 (OCTN1) transporter.

Biochim Biophys Acta. 2016-4

[4]
The human OCTN1 (SLC22A4) reconstituted in liposomes catalyzes acetylcholine transport which is defective in the mutant L503F associated to the Crohn's disease.

Biochim Biophys Acta. 2012-3

[5]
Effect of Cholesterol on the Organic Cation Transporter OCTN1 (SLC22A4).

Int J Mol Sci. 2020-2-6

[6]
Regulation by physiological cations of acetylcholine transport mediated by human OCTN1 (SLC22A4). Implications in the non-neuronal cholinergic system.

Life Sci. 2012-4-30

[7]
OCTN1 (SLC22A4) displays two different transport pathways for organic cations or zwitterions.

Biochim Biophys Acta Biomembr. 2024-2

[8]
LPS-induced inflammation delays the transportation of ASP due to down-regulation of OCTN1/2 in alveolar epithelial cells.

J Drug Target. 2020-4

[9]
Novel membrane transporter OCTN1 mediates multispecific, bidirectional, and pH-dependent transport of organic cations.

J Pharmacol Exp Ther. 1999-5

[10]
Modulation of drug block of the cardiac potassium channel KCNA5 by the drug transporters OCTN1 and MDR1.

Br J Pharmacol. 2010-11

本文引用的文献

[1]
Atomistic description of the OCTN1 recognition mechanism via in silico methods.

PLoS One. 2024

[2]
Inflammation and Organic Cation Transporters Novel (OCTNs).

Biomolecules. 2024-3-25

[3]
Membrane transporters in drug development and as determinants of precision medicine.

Nat Rev Drug Discov. 2024-4

[4]
OCTN1 (SLC22A4) displays two different transport pathways for organic cations or zwitterions.

Biochim Biophys Acta Biomembr. 2024-2

[5]
Transport and inhibition mechanism of the human SGLT2-MAP17 glucose transporter.

Nat Struct Mol Biol. 2024-1

[6]
A549 as an In Vitro Model to Evaluate the Impact of Microplastics in the Air.

Biology (Basel). 2023-9-15

[7]
Structure-based discovery of conformationally selective inhibitors of the serotonin transporter.

Cell. 2023-5-11

[8]
Insights into the Transport Cycle of LAT1 and Interaction with the Inhibitor JPH203.

Int J Mol Sci. 2023-2-17

[9]
Role of non-neuronal cholinergic system in the early stage response of epithelial-mesenchymal transformation related markers in A549 cells induced by coal particles.

Heliyon. 2022-11-23

[10]
Current Landscape of Therapeutic Resistance in Lung Cancer and Promising Strategies to Overcome Resistance.

Cancers (Basel). 2022-9-20

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