School of Life Science, Shanxi University, Taiyuan, China.
Department of Environmental Resources, Chia Nan University of Pharmacy and Science, Taiwan, Republic of China.
Int J Biol Macromol. 2023 Aug 30;247:125745. doi: 10.1016/j.ijbiomac.2023.125745. Epub 2023 Jul 7.
P-glycoprotein (Pgp), a member of ATP binding cassette (ABC) transporter family, can extrude toxic substances out of cells by mediating multi-xenobiotic resistance (MXR) in aquatic organisms, however, its regulation and association with MXR are still unclear. In this work, the genetic information of Pgp in freshwater crab Sinopotamon henanense (ShPgp) was revealed for the first time. ShPgp with a total of 4488 bp was cloned and analyzed, which includes 4044 bp open reading frame, 353 bp 3' untranslated region, and 91 bp 5' untranslated region. The recombinant ShPGP were expressed in Saccharomyces cerevisiae and taken for SDS-PAGE and western blot analysis. ShPGP was widely expressed in the midgut, hepatopancreas, testis, ovary, gill, hemocytes, accessory gonad and myocardium of the crabs studied. The images of immunohistochemistry indicated that ShPgp was mainly distributed in the cytoplasm and cell membrane. When the crabs were exposed to cadmium or cadmium containing quantum dots (Cd-QDs), not only the relative expression of ShPgp mRNA and the protein produced were enhanced, but also the MXR activity and ATP contents. The relative expression of target genes related to energy metabolism, detoxification and apoptosis was also determined in the carbs exposed to Cd or Cd-QDs. The results showed that bcl-2 was significantly down-regulated, while other genes were up-regulated except PPAR (not affected). However, when the Shpgp in treated crabs was interfering by knockdown technique, their apoptosis and the expression of proteolytic enzyme genes and transcription factors MTF1 and HSF1 were also elevated, while the expression of apoptosis inhibiting and fat metabolism genes were compromised. Based on the observation, we concluded that MTF1 and HSF1 were involved in gene transcription regulation of mt and MXR, respectively, while PPAR had limited regulatory effect on those genes in S. henanense. NF-κB may play a negligible role in the process of apoptosis in testes induced by cadmium or Cd-QDs. However, the detail information regarding Pgp involvement in SOD or MT, and its association with apoptosis during xenobiotics insults remain to be explored.
P-糖蛋白(Pgp)是 ATP 结合盒(ABC)转运体家族的成员,可通过介导水生生物的多外源性耐药(MXR)将有毒物质排出细胞外,但其调节及其与 MXR 的关系尚不清楚。在这项工作中,首次揭示了淡水蟹河南华溪蟹(ShPgp)的 Pgp 遗传信息。克隆并分析了全长为 4488bp 的 ShPgp,其中包括 4044bp 的开放阅读框、353bp 的 3'非翻译区和 91bp 的 5'非翻译区。重组 ShPGP 在酿酒酵母中表达,并进行 SDS-PAGE 和 Western blot 分析。ShPGP 在研究蟹的中肠、肝胰腺、睾丸、卵巢、鳃、血细胞、副性腺和心肌中广泛表达。免疫组织化学图像表明,ShPgp 主要分布在细胞质和细胞膜中。当蟹暴露于镉或含镉量子点(Cd-QDs)时,不仅 Shpgp mRNA 的相对表达和产生的蛋白质增加,而且 MXR 活性和 ATP 含量也增加。还测定了暴露于 Cd 或 Cd-QDs 的蟹中与能量代谢、解毒和细胞凋亡相关的靶基因的相对表达。结果表明,bcl-2 显著下调,而其他基因除 PPAR 外(不受影响)均上调。然而,当用敲低技术干扰处理蟹中的 Shpgp 时,它们的凋亡以及蛋白酶基因和转录因子 MTF1 和 HSF1 的表达也升高,而凋亡抑制和脂肪代谢基因的表达则受到损害。基于观察结果,我们得出结论,MTF1 和 HSF1 分别参与 mt 和 MXR 的基因转录调节,而 PPAR 对河南华溪蟹中这些基因的调节作用有限。NF-κB 在镉或 Cd-QDs 诱导的睾丸细胞凋亡过程中可能不起作用。然而,有关 Pgp 参与 SOD 或 MT 以及在外源物胁迫下与凋亡的关系的详细信息仍有待探索。