# Proliferation capability of natural killer cells upon cytokines stimulation correlated negatively with serum lactate dehydrogenase level in coronary artery disease patients

**Authors:** Xuemin Guo, Ting Xiao, Li Lin, Qianqian Gao, Bifa Lai, Xianhui Liu, Zhixiong Zhong

PMC · DOI: 10.3389/fimmu.2024.1436747 · 2024-09-02

## TL;DR

This study found that ascorbic acid boosts natural killer cell proliferation in coronary artery disease patients, and higher lactate dehydrogenase levels correlate with lower NK cell proliferation.

## Contribution

The study reveals a negative correlation between serum LDH levels and NK cell proliferation in CAD patients, and identifies ascorbic acid as a stimulator of NK cell proliferation.

## Key findings

- Ascorbic acid treatment significantly increased NK cell proliferation in 28 out of 29 CAD patient samples.
- Serum lactate dehydrogenase levels negatively correlated with NK cell proliferation upon interleukin stimulation.
- LDH addition to NK cells enhanced production of IFN-γ, IL-10, and TNF-α, indicating a regulatory role.

## Abstract

Natural killer (NK) cells are proposed to participate in coronary artery disease (CAD) development. However, little is known about how CAD patients’ NK cells respond to different stimulatory factors in terms of proliferation capability.

Twenty-nine CAD patients’ peripheral blood NK cells were isolated and individually treated with IL-2, IL-12, IL-15, IL-18, IL-21, cortisone acetate, hydrocortisone, or ascorbic acid for 36 hours, followed by cell cycle analysis using flow cytometry. The ratio of S and G2/M phase cell number to total cell number was defined as a proliferation index (PrI) and used for proliferative capability indication. The results showed that these eight factors resulted in different life cycle changes in the 29 NK cell samples. Remarkably, 28 out of 29 NK cell samples showed an obvious increase in PrI upon ascorbic acid treatment. The serum lactate dehydrogenase (LDH) level of the 29 CAD patients was measured. The results showed a negative correlation between serum LDH level and the CAD patients’ NK cell PrI upon stimulation of interleukins, but not the non-interleukin stimulators. Consistently, a retrospective analysis of 46 CAD patients and 32 healthy donors showed that the circulating NK cell number negatively correlated with the serum LDH level in CAD patients. Unexpectedly, addition of LDH to NK cells significantly enhanced the production of IFN-γ, IL-10 and TNF-α, suggesting a strong regulatory role on NK cell’s function.

Ascorbic acid could promote the proliferation of the CAD patients’ NK cells; LDH serum level may function as an indicator for NK cell proliferation capability and an immune-regulatory factor.

## Linked entities

- **Proteins:** IFNG (interferon gamma), IL10 (interleukin 10), TNF (tumor necrosis factor), Ldh (Lactate dehydrogenase)
- **Chemicals:** IL-2 (PubChem CID 51397006), cortisone acetate (PubChem CID 5745), hydrocortisone (PubChem CID 5754), ascorbic acid (PubChem CID 9888239)
- **Diseases:** coronary artery disease (MONDO:0005010)

## Full-text entities

- **Genes:** IL2 (interleukin 2) [NCBI Gene 3558] {aka IL-2, TCGF, lymphokine}, IL18 (interleukin 18) [NCBI Gene 3606] {aka IGIF, IL-18, IL-1g, IL1F4}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, IL21 (interleukin 21) [NCBI Gene 59067] {aka CVID11, IL-21, Za11}, IL12B (interleukin 12B) [NCBI Gene 3593] {aka CLMF, CLMF2, IL-12B, IMD28, IMD29, NKSF}, IL15 (interleukin 15) [NCBI Gene 3600] {aka IL-15}, IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}
- **Diseases:** CAD (MESH:D003324)
- **Chemicals:** cortisone acetate (MESH:D003348), hydrocortisone (MESH:D006854), Ascorbic acid (MESH:D001205)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11402710/full.md

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Source: https://tomesphere.com/paper/PMC11402710