Lactiplantibacillus plantarum K8 lysates regulate hypoxia-induced gene expression

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作者
Jaehyeon Jeong
Byeong-Hee Kang
Sangmin Ju
Na Yeon Park
Deukyeong Kim
Ngoc Thi Bao Dinh
Jeongho Lee
Chang Yun Rhee
Dong-Hyung Cho
Hangeun Kim
Dae Kyun Chung
Heeyoun Bunch
机构
[1] Kyungpook National University,Department of Applied Biosciences
[2] Kyungpook National University,School of Applied Biosciences, College of Agriculture and Life Sciences
[3] Kyungpook National University,School of Life Sciences, BK21 FOUR KNU Creative BioRearch Group
[4] Skin Biotechnology Center Co. Ltd.,Research and Development Center
[5] Kyung Hee University,Graduate School of Biotechnology
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关键词
Hypoxic gene expression; HIF1α; Transcriptional regulation; Natural hypoxic response suppressor;
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摘要
Hypoxic responses have been implicated in critical pathologies, including inflammation, immunity, and tumorigenesis. Recently, efforts to identify effective natural remedies and health supplements are increasing. Previous studies have reported that the cell lysates and the cell wall-bound lipoteichoic acids of Lactiplantibacillus plantarum K8 (K8) exert anti-inflammatory and immunomodulative effects. However, the effect of K8 on cellular hypoxic responses remains unknown. In this study, we found that K8 lysates had a potent suppressive effect on gene expression under hypoxia. K8 lysates markedly downregulated hypoxia-induced HIF1α accumulation in the human bone marrow and lung cancer cell lines, SH-SY5Y and H460. Consequently, the transcription of known HIF1α target genes, such as p21, GLUT1, and ALDOC, was notably suppressed in the K8 lysate supplement and purified lipoteichoic acids of K8, upon hypoxic induction. Intriguingly, K8 lysates decreased the expression of PHD2 and VHL proteins, which are responsible for HIF1α destabilization under normoxic conditions, suggesting that K8 may regulate HIF1α stability in a non-canonical pathway. Overall, our results suggest that K8 lysates desensitize the cells to hypoxic stresses and suppress HIF1α-mediated hypoxic gene activation.
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