Protective Effects of Choline against Inflammatory Cytokines and Characterization of Transport in Motor Neuron-like Cell Lines (NSC-34)

Choline, a component of the neurotransmitter acetylcholine, is essential for nervous system functions, brain development, and gene expression. In our study, we investigated the protective effect and transport characteristics of choline in amyotrophic lateral sclerosis (ALS) model cell lines. We used...

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Main Authors: Sana Latif, Young-Sook Kang
Format: Article
Language:English
Published: MDPI AG 2022-11-01
Series:Pharmaceutics
Subjects:
Online Access:https://www.mdpi.com/1999-4923/14/11/2374
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author Sana Latif
Young-Sook Kang
author_facet Sana Latif
Young-Sook Kang
author_sort Sana Latif
collection DOAJ
description Choline, a component of the neurotransmitter acetylcholine, is essential for nervous system functions, brain development, and gene expression. In our study, we investigated the protective effect and transport characteristics of choline in amyotrophic lateral sclerosis (ALS) model cell lines. We used the wild-type (WT) motor neuron-like hybrid cell line (NSC-34/hSOD1<sup>WT</sup>) as a control and the mutant-type (MT; NSC-34/hSOD1<sup>G93A</sup>) as a disease model. The uptake of [<sup>3</sup>H]choline was time-, pH-, and concentration-dependent. [<sup>3</sup>H]Choline transport was sodium-dependent, and, upon pretreatment with valinomycin, induced membrane depolarization. Gene knockdown of Slc44a1 revealed that choline-like transporter 1 (CTL1) mediates the transport of choline. In NSC-34 cell lines, the specific choline transporter inhibitor, hemicholinium-3 demonstrated significant inhibition. Donepezil and nifedipine caused dose-dependent inhibition of [<sup>3</sup>H]choline uptake by the MT cell line with minimal half inhibitory concentration (IC<sub>50</sub>) values of 0.14 mM and 3.06 mM, respectively. Four-day pretreatment with nerve growth factor (NGF) resulted in an inhibitory effect on [<sup>3</sup>H]choline uptake. Choline exerted protective and compensatory effects against cytokines mediators. Hence, the choline transport system CLT1 may act as a potential target for the delivery of novel pharmacological drugs, and the combination of drugs with choline can help treat symptoms related to ALS.
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spelling doaj.art-f10b462652244284b183979816fa081d2023-11-24T06:21:13ZengMDPI AGPharmaceutics1999-49232022-11-011411237410.3390/pharmaceutics14112374Protective Effects of Choline against Inflammatory Cytokines and Characterization of Transport in Motor Neuron-like Cell Lines (NSC-34)Sana Latif0Young-Sook Kang1Research Institute of Pharmaceutical Sciences, College of Pharmacy, Sookmyung Women’s University, 100 Cheongpa-ro 47-gil, Yongsan-gu, Seoul 04310, KoreaResearch Institute of Pharmaceutical Sciences, College of Pharmacy, Sookmyung Women’s University, 100 Cheongpa-ro 47-gil, Yongsan-gu, Seoul 04310, KoreaCholine, a component of the neurotransmitter acetylcholine, is essential for nervous system functions, brain development, and gene expression. In our study, we investigated the protective effect and transport characteristics of choline in amyotrophic lateral sclerosis (ALS) model cell lines. We used the wild-type (WT) motor neuron-like hybrid cell line (NSC-34/hSOD1<sup>WT</sup>) as a control and the mutant-type (MT; NSC-34/hSOD1<sup>G93A</sup>) as a disease model. The uptake of [<sup>3</sup>H]choline was time-, pH-, and concentration-dependent. [<sup>3</sup>H]Choline transport was sodium-dependent, and, upon pretreatment with valinomycin, induced membrane depolarization. Gene knockdown of Slc44a1 revealed that choline-like transporter 1 (CTL1) mediates the transport of choline. In NSC-34 cell lines, the specific choline transporter inhibitor, hemicholinium-3 demonstrated significant inhibition. Donepezil and nifedipine caused dose-dependent inhibition of [<sup>3</sup>H]choline uptake by the MT cell line with minimal half inhibitory concentration (IC<sub>50</sub>) values of 0.14 mM and 3.06 mM, respectively. Four-day pretreatment with nerve growth factor (NGF) resulted in an inhibitory effect on [<sup>3</sup>H]choline uptake. Choline exerted protective and compensatory effects against cytokines mediators. Hence, the choline transport system CLT1 may act as a potential target for the delivery of novel pharmacological drugs, and the combination of drugs with choline can help treat symptoms related to ALS.https://www.mdpi.com/1999-4923/14/11/2374amyotrophic lateral sclerosischolineNSC-34 cell linescholine-like transportersinflammatory cytokinesnerve growth factor
spellingShingle Sana Latif
Young-Sook Kang
Protective Effects of Choline against Inflammatory Cytokines and Characterization of Transport in Motor Neuron-like Cell Lines (NSC-34)
Pharmaceutics
amyotrophic lateral sclerosis
choline
NSC-34 cell lines
choline-like transporters
inflammatory cytokines
nerve growth factor
title Protective Effects of Choline against Inflammatory Cytokines and Characterization of Transport in Motor Neuron-like Cell Lines (NSC-34)
title_full Protective Effects of Choline against Inflammatory Cytokines and Characterization of Transport in Motor Neuron-like Cell Lines (NSC-34)
title_fullStr Protective Effects of Choline against Inflammatory Cytokines and Characterization of Transport in Motor Neuron-like Cell Lines (NSC-34)
title_full_unstemmed Protective Effects of Choline against Inflammatory Cytokines and Characterization of Transport in Motor Neuron-like Cell Lines (NSC-34)
title_short Protective Effects of Choline against Inflammatory Cytokines and Characterization of Transport in Motor Neuron-like Cell Lines (NSC-34)
title_sort protective effects of choline against inflammatory cytokines and characterization of transport in motor neuron like cell lines nsc 34
topic amyotrophic lateral sclerosis
choline
NSC-34 cell lines
choline-like transporters
inflammatory cytokines
nerve growth factor
url https://www.mdpi.com/1999-4923/14/11/2374
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