Skip to main content

Advertisement

Log in

The effects of pro-inflammatory cytokines and glutamate on l-arginine transport in a human microglial cell line (HMC-3)

  • Original Article
  • Published:
Journal of Pharmaceutical Investigation Aims and scope Submit manuscript

Abstract

Purpose

Neuroinflammation and microglial activation are the key factors in neurodegenerative motor neuron diseases. Microglial activation has been link to disease progression in humans. This study investigated the transport and potential effects of l-arginine under pathological conditions in a human microglial cell line.

Methods

Transport study was performed using [3H]l-arginine isotope and uptake was measured in the human microglial clone 3 (HMC-3) cell line. MTT assay was performed for cell viability analysis. mRNA expression of cationic amino acid transporter-1 (CAT-1) was also determined.

Results

The transport of l-arginine was time- and concentration-dependent in HMC-3 cell lines. Kinetic parameters revealed carrier-mediated arginine transport via CAT-1, with high affinity and low capacity at high-affinity sites and low affinity and high capacity at low-affinity sites. HMC-3 cells pretreated with glutamate exhibited decreased viability. [3H]l-arginine uptake increased markedly with glutamate pretreatment, whereas co-treatment with arginine further increased the uptake. After tumor necrosis factor α and lipopolysaccharide pretreatment, [3H]l-arginine uptake significantly increased. In contrast, the uptake was significantly decreased after co-treatment of the cells with unlabeled l-arginine. The mRNA expression of CAT-1 showed a similar uptake pattern. Various pharmacological drugs including donepezil, quinidine, verapamil and tramadol significantly inhibited the uptake of [3H]l-arginine in HMC-3 cell line.

Conclusion

These results suggest that l-arginine supplementation may play an effective role against inflammatory states in neurodegenerative diseases.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4

Similar content being viewed by others

Data availability

The data that support the findings of this study are included in this article.

References

Download references

Acknowledgements

The authors thank Dr. Ryu Hoon from the Korea Institute of Science and Technology for providing the cell lines. This work was supported by the National Research Foundation of Korea (NRF) grant funded by the Korean government (MSIT) (No. 2019R1F1A1044048) (YSK).

Author information

Authors and Affiliations

Authors

Contributions

YSK conceived and designed the experiments and wrote and reviewed the manuscript. SL performed the experiments, collected and analyzed the data, and wrote the manuscript. All the authors have read and approved the final manuscript.

Corresponding author

Correspondence to Young-Sook Kang.

Ethics declarations

Conflict of interest

All authors (S. Latif and Y.S. Kang) declare no conflict of interest.

Statement of human and animal rights

This article does not contain any studies with human and animal subjects performed by any of the authors.

Additional information

Publisher’s Note

Springer nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Latif, S., Kang, YS. The effects of pro-inflammatory cytokines and glutamate on l-arginine transport in a human microglial cell line (HMC-3). J. Pharm. Investig. 54, 77–84 (2024). https://doi.org/10.1007/s40005-023-00648-5

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s40005-023-00648-5

Keywords

Navigation