Exposure to Nanoplastics Cause Caudal Vein Plexus Damage and Hematopoietic Dysfunction by Oxidative Stress Response in Zebrafish (Danio rerio)

Int J Nanomedicine. 2024 Dec 21:19:13789-13803. doi: 10.2147/IJN.S485091. eCollection 2024.

Abstract

Introduction: The proliferation of nanoplastics (NPs) has emerged as a significant environmental concern due to their extensive use, raising concerns about potential adverse effects on human health. However, the exact impacts of NPs on the early development of hematopoietic organs remain poorly understood.

Methods: This investigation utilized fluorescence microscopy to observe the effects of various NP concentrations on the caudal vein plexus (CVP) development in zebrafish embryos. Subsequent RNA sequencing (RNA-seq) identified genes related to CVP deformities and hematopoietic stem/progenitor cells (HSPCs) in zebrafish embryos exposed to NPs. Additionally, single cell RNA sequencing (scRNA-seq) analysis identified genes associated with the development of CVP and HSPCs. RT-qPCR assessed changes in expression of these genes in zebrafish embryos exposed to different NP concentrations.

Results: The impact of NPs on zebrafish embryos was investigated, revealing significant reductions in survival and hatching rates and decreases in body length alongside increased heart rates. Exposure to NPs at 8 mg/L severely impaired zebrafish CVP development. RNA-seq revealed that NPs exposure altered the activity of oxidative enzymes, hydrolases, and the extracellular matrix in zebrafish embryos. Treatment with 10 µM NAC effectively rescued the CVP defects induced by NPs. Additionally, scRNA-seq identified genes associated with EC and HSPC development, and subsequent RT-qPCR validation confirmed significant expression changes in these genes.

Conclusion: The results of this study suggest that NPs induce oxidative stress in vascular ECs and HSPCs, which mediates CVP damage and impairs hematopoiesis in zebrafish embryos.

Keywords: caudal vein plexus; endothelial cells; hematopoietic stem/progenitor cells; nanoplastics; oxidative stress; single cell RNA sequencing; zebrafish.

MeSH terms

  • Animals
  • Embryo, Nonmammalian* / drug effects
  • Hematopoiesis / drug effects
  • Hematopoietic Stem Cells / drug effects
  • Microplastics / toxicity
  • Nanoparticles / toxicity
  • Oxidative Stress* / drug effects
  • Veins / drug effects
  • Veins / embryology
  • Zebrafish* / embryology

Substances

  • Microplastics