2. Academic Validation
  3. IRE1 and CaMKKβ pathways to reveal the mechanism involved in microcystin-LR-induced autophagy in mouse ovarian cells

IRE1 and CaMKKβ pathways to reveal the mechanism involved in microcystin-LR-induced autophagy in mouse ovarian cells

  • Food Chem Toxicol. 2021 Jan;147:111911. doi: 10.1016/j.fct.2020.111911.
Ya Ma 1,  Haohao Liu 1,  Xingde Du 1,  Pavankumar Petlulu 2,  Xinghai Chen 3,  Rui Wang 1,  Shiyu Zhang 1,  Zhihui Tian 1,  Linjia Shi 1,  Hongxiang Guo 4,  Huizhen Zhang 5
Affiliations

Affiliations

  • 1 College of Public Health, Zhengzhou University, Zhengzhou, Henan 450001, PR China.
  • 2 University of Texas Southwestern Medical Center, Dallas, TX 75201, USA.
  • 3 Department of Chemistry and Biochemistry, St Mary's University, San Antonio, TX 78264, USA.
  • 4 College of Life Sciences, Henan Agricultural University, Zhengzhou, Henan 450002, PR China.
  • 5 College of Public Health, Zhengzhou University, Zhengzhou, Henan 450001, PR China. Electronic address: [email protected].
PMID: 33290805 DOI: 10.1016/j.fct.2020.111911
Abstract

Microcystin-LR (MC-LR) is an emerging water pollutant produced by blooming cyanobacteria. It could be absorbed into human body via contaminated food and drinking water causing severe reproductive toxicity. Previous studies showed that MC-LR could regulate Autophagy by inducing endoplasmic reticulum (ER) stress thereby causing female reproductive toxicity. However, the molecular mechanisms of MC-LR-induced Autophagy remain to be elucidated. It is known that IRE1 and CaMKKβ pathways are two important pathways involved in Autophagy induced by ER stress. Hence, this study investigated the roles of both pathways in MC-LR-induced Autophagy in mouse ovarian cells. The results showed that MC-LR significantly up-regulated the expression of Autophagy marker proteins LC3Ⅱ and Beclin1 and down-regulated the expression of P62 in vivo and in vitro. MC-LR-caused increase of autophagosomes could be observed in KK-1 cells by MDC staining. MC-LR induced the formation of autolysosomes as indicated by the overlap of LAMP1 and LC3. Meanwhile, MC-LR significantly activated the proteins in IRE1 pathway (IRE1, XBP1 and JNK) and in CaMKKβ pathway (CaMKKβ, AMPK, mTOR). Furthermore, MC-LR caused weight loss and ovarian histopathological damage in mice. In contrast, after the expression and function of IRE1 and CaMKKβ were inhibited with siRNA in vitro and by inhibitors (4μ8C and STO-609, respectively) in vivo, the up-regulation of LC3Ⅱ and Beclin1 and the degradation of P62 induced by MC-LR were significantly suppressed. MC-LR-induced autophagosomes in KK-1 cells and autolysosomes in mouse ovarian cells were also decreased. Moreover, the knockdown of IRE1 and CaMKKβ relieved MC-LR-induced histopathological injury to mouse ovaries. These results indicated that MC-LR induced ovarian cell Autophagy and ovarian injury via IRE1 and CaMKKβ pathways. This study is the first study revealing the molecular mechanisms of MC-LR-induced Autophagy of ovarian cells and providing new insights into the female reproductive toxicity of MC-LR.

Keywords

Ca(2+)/calmodulin-dependent protein kinase kinase; autophagy; inositol-requiring enzyme 1; microcystin-LR; reproductive toxicity.

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