Pyruvate dehydrogenase kinase 1 regulates the function of human decidual natural killer cells

穿孔素 颗粒酶B 乳酸脱氢酶 颗粒酶 生物 细胞生物学 免疫系统 癌症研究 分子生物学 T细胞 免疫学 CD8型 生物化学
作者
Huirong Li,Linghui Cheng,Shiyue Su,Peipei Guo,Zhaolian Wei
出处
期刊:American Journal of Reproductive Immunology [Wiley]
卷期号:90 (4): e13765-e13765 被引量:3
标识
DOI:10.1111/aji.13765
摘要

Abstract Problem Pyruvate dehydrogenase kinase 1 (PDK1) is an important enzyme for immune cell development. However, PDK1's role in human decidual natural killer (dNK) cells remains largely unknown. Methods of study PDK1 expression in dNK cells from patients with recurrent spontaneous abortions (RSA) and age‐matched healthy controls was analyzed by qRT‐PCR, western bolt and flow cytometry. Moreover, dNK cells were treated with PDK1 inhibitor or the PDK1 siRNA followed by functional assays. Results The dNK cells from patients who underwent RSAs had higher mRNA expression and increased protein of PDK1, perforin (PRF1), Granzyme B (GZMB), IFN‐γ (IFNG), and CD107a expression compared to dNK cells from age‐matched healthy controls. Perforin, Granzyme B, IFN‐γ and CD107a expression levels in dNK cells were down‐regulated when dNK cells were treated with a PDK1 inhibitor. As measured by the 51 Cr release assay, the killing activity of dNK cells was found to be decreased. We also demonstrated that PDK1 blockade could up‐regulate the migration and adhesion of dNK cells. Furthermore, PDK1 inhibition reduced the glycolysis of dNK cells. Conclusion This study suggested that PDK1 plays an important role in regulating dNK cell functions and human RSA.
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