Sedoheptulose kinase bridges the pentose phosphate pathway and immune responses in pathogen-challenged sea cucumber Apostichopus japonicus

The sedoheptulose kinase carbohydrate kinase-like protein (CARKL) is critical for immune cell activation, reactive oxygen species (ROS) production, and cell polarization by restricting flux through the pentose phosphate pathway (PPP). To date, little is known about CARKL in regulating immune respons...

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Veröffentlicht in:Developmental and comparative immunology 2020-08, Vol.109, p.103694-103694, Article 103694
Hauptverfasser: Sun, Lianlian, Zhou, Fangyuan, Shao, Yina, Lv, Zhimeng, Li, Chenghua
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Sprache:eng
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Zusammenfassung:The sedoheptulose kinase carbohydrate kinase-like protein (CARKL) is critical for immune cell activation, reactive oxygen species (ROS) production, and cell polarization by restricting flux through the pentose phosphate pathway (PPP). To date, little is known about CARKL in regulating immune responses in marine invertebrates. In this study, we first cloned and characterized the CARKL gene from Apostichopus japonicus (designated as AjCARKL). Time-course analysis revealed that Vibrio splendidus challenge in vivo and lipopolysaccharide stimulation in vitro significantly downregulated AjCARKL mRNA expression. Furthermore, AjCARKL overexpression in cultured coelomocytes not only significantly inhibited the mRNA expression level of the rate-limiting enzyme glucose-6-phosphate dehydrogenase of the PPP but sharply decreased coelomocyte proliferation, ROS production, and phagocytic rate. Additionally, AjCARKL overexpression in mouse peritoneal macrophages (RAW264.7 cells) significantly attenuated the intracellular ROS production and sensitized the M2 phenotype macrophage polarization. These results revealed that AjCARKL serves as a rheostat for cellular metabolism and is required for proper immune response by negatively regulating PPP in pathogen-challenged A. japonicus. •Both Vibrio splendidus challenge and LPS treatment could downregulate AjCARKL expression.•AjCARKL overexpression restricts ROS and coelomocyte phagocytosis by negatively regulating PPP flux.•AjCARKL overexpression represses IL-1β and ROS, but induce IL-10 expression in RAW264.7 cells.•AjCARK overexpression sensitizes M2 phenotype polarization in RAW264.7 cells.
ISSN:0145-305X
1879-0089
DOI:10.1016/j.dci.2020.103694