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Effect of transforming growth factor-β1 on functional expression of monocarboxylate transporter 1 in alveolar epithelial A549 cells

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Abstract

Epithelial-mesenchymal transition (EMT) contributes to the development of severe lung diseases, such as pulmonary fibrosis. Recently, it has been reported that EMT involves complex metabolic reprogramming triggered by several factors including transforming growth factor (TGF-β1) and that monocarboxylate transporter (MCT1) plays an essential role in these metabolic changes. The aim of the present study was to clarify the functional expression of MCT1 during TGF-β1-induced EMT in alveolar epithelial A549 cells. The transport function of MCT1 in A549 cells was examined using [3H]γ-hydroxybutyrate (GHB) and [3H] lactic acid (LA) as substrates and α-cyano-4-hydroxycinnamate (CHC), lactic acid, phloretin, and AR-C155858 (AR) as inhibitors of MCT1. EMT was induced by treating the cells with TGF-β1. mRNA and protein expression levels were analyzed using real-time PCR and Western blotting, respectively. Time-, temperature-, and pH-dependent GHB and LA uptake were observed in A549 cells. CHC, lactic acid, phloretin, and AR significantly inhibited the uptake of GHB in a concentration-dependent manner, suggesting that MCT1 is primarily responsible for transport of monocarboxylates such as GHB and LA in A549 cells. TGF-β1 treatment significantly enhanced GHB and LA uptake as well as the mRNA and protein expression levels of MCT1 in A549 cells. These changes were neutralized by co-treatment with SB431542, an inhibitor for the TGF-β1 signaling pathway. CHC and AR had no effect on TGF-β1-induced EMT-related gene expression changes. Here, we have clearly characterized functional expression of MCT1 in A549 cells and have shown that MCT1 may be upregulated via the TGF-β1 signaling pathway.

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Abbreviations

CK19:

cytokeratin 19

EMT:

epithelial-mesenchymal transition

GHB:

γ-hydroxybutyrate

SB:

SB431542

α-SMA:

α-smooth muscle actin

TGF-β1:

transforming growth factor-β1

GAPDH:

glyceraldehyde-3-phosphate dehydrogenase

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Funding

This work was supported in part by a Grant-in-Aid for Scientific Research from the Japan Society for the Promotion of Sciences (JSPS) (numbers; 26293033, 15 K08074, and 16 K18945).

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MU and MK designed and performed the experiments, analyzed the data, and wrote the manuscript. RY and MT discussed the results and edited and approved the manuscript.

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Correspondence to Mikihisa Takano.

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The authors declare that they have no conflict of interest.

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Uddin, M., Kawami, M., Yumoto, R. et al. Effect of transforming growth factor-β1 on functional expression of monocarboxylate transporter 1 in alveolar epithelial A549 cells. Naunyn-Schmiedeberg's Arch Pharmacol 393, 889–896 (2020). https://doi.org/10.1007/s00210-019-01802-3

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  • DOI: https://doi.org/10.1007/s00210-019-01802-3

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