Key Laboratory of Environmental Medicine Engineering of Ministry of Education, School of Public Health, Southeast University, Nanjing, China.
Key Laboratory of Environmental Medicine Engineering of Ministry of Education, School of Public Health, Southeast University, Nanjing, China.
Sci Total Environ. 2024 Sep 10;942:173746. doi: 10.1016/j.scitotenv.2024.173746. Epub 2024 Jun 6.
As a member of biodegradable plastics, exposure risk of polylactic acid microplastic (PLA-MP) has received attention recently. Toxicity of PLA-MP at parental generation (P0-G) has been observed in some organisms; however, its possible transgenerational toxicity and underlying mechanisms remain unclear. In Caenorhabditis elegans, 10 and 100 μg/L PLA-MP resulted in transgenerational inhibition in reproductive capacity and transgenerational damage on gonad development. Meanwhile, transgenerational increase in germline apoptosis was detected after PLA-MP exposure at P0-G, which was associated with transgenerational dysregulation in expressions of genes governing apoptosis (ced-3, ced-4, egl-1, and ced-9) and DNA damage related genes (cep-1, mrt-2, hus-1, and clk-2). Among secreted ligand genes, PLA-MP exposure induced transgenerational increase in expression of ins-39 and wrt-3, and RNAi of ins-39 and wrt-3 inhibited germline apoptosis in PLA-MP exposed nematodes. Additionally, PLA-MP caused transgenerational increase in expression of met-2 and set-6 encoding histone methylation transferases, and germline apoptosis induced by PLA-MP could be suppressed by RNAi of met-2 and set-6. Dysregulated expressions of some apoptosis and DNA damage related genes caused by PLA-MP were reversed by RNAi of ins-39, wrt-3, met-2, and set-6. Moreover, in PLA-MP exposed animals, expression of ins-39 and wrt-3 could be further inhibited by RNAi of met-2 and set-6. Therefore, PLA-MP potentially induced reproductive toxicity across multiple generations, which was under the control of MET-2 and SET-6 activated ligands of INS-39 and WRT-3.
作为可生物降解塑料的一员,聚乳酸微塑料(PLA-MP)的暴露风险最近受到了关注。已经在一些生物体中观察到 PLA-MP 对亲代(P0-G)的毒性;然而,其可能的跨代毒性及其潜在机制尚不清楚。在秀丽隐杆线虫中,10 和 100μg/L 的 PLA-MP 导致生殖能力的跨代抑制和性腺发育的跨代损伤。同时,在 P0-G 暴露于 PLA-MP 后检测到生殖细胞凋亡的跨代增加,这与凋亡(ced-3、ced-4、egl-1 和 ced-9)和 DNA 损伤相关基因(cep-1、mrt-2、hus-1 和 clk-2)的调控异常有关。在分泌配体基因中,PLA-MP 暴露诱导 ins-39 和 wrt-3 的表达跨代增加,并且 ins-39 和 wrt-3 的 RNAi 抑制 PLA-MP 暴露线虫中的生殖细胞凋亡。此外,PLA-MP 导致编码组蛋白甲基转移酶的 met-2 和 set-6 的表达跨代增加,并且 PLA-MP 诱导的生殖细胞凋亡可以通过 met-2 和 set-6 的 RNAi 抑制。PLA-MP 引起的一些凋亡和 DNA 损伤相关基因的失调表达可以通过 ins-39、wrt-3、met-2 和 set-6 的 RNAi 逆转。此外,在暴露于 PLA-MP 的动物中,ins-39 和 wrt-3 的表达可以进一步被 met-2 和 set-6 的 RNAi 抑制。因此,PLA-MP 可能通过 MET-2 和 SET-6 激活 INS-39 和 WRT-3 的配体来诱导跨代生殖毒性。