Induction of caspase-2 gene expression in carboxyl-functionalized carbon nanotube-treated human T-cell leukemia

Shirin Lotfipanah1, Majid Zeinali2, Parichehreh Yaghmaei1

  • 1Department of Biology, Science and Research Branch, Islamic Azad University, Tehran, Iran.

Insights

Carboxylated carbon nanotubes (CNTs) showed mild toxicity to Jurkat cells. Multi-walled CNTs significantly increased Caspase-2 (Cas2) gene expression, suggesting a unique cell death pathway distinct from typical apoptosis.

Area of Science:

  • Biomedical Engineering
  • Nanotechnology
  • Toxicology

Background:

  • Carbon nanotubes (CNTs) offer potential in biomedicine but require thorough toxicity assessment.
  • Apoptosis, mediated by caspases, is a key cellular pathway affected by toxic agents.

Purpose of the Study:

  • To investigate the cellular toxicity of carboxyl-functionalized single-walled (SWCNT) and multi-walled (MWCNT) carbon nanotubes on Jurkat cells.
  • To evaluate the impact of these CNTs on the gene expression of selected caspases.

Main Methods:

  • Jurkat cells were exposed to 100 µg/mL carboxylated SWCNTs and MWCNTs for 72 hours.
  • Cell viability was assessed using the MTT assay.
  • Caspase gene expression levels were quantified using qRT-PCR, with β-actin and GAPDH as normalization controls.

Main Results:

  • Carboxylated MWCNTs induced a mild decrease in Jurkat cell viability.
  • QRT-PCR revealed a significant 6.08-fold increase in Caspase-2 (Cas2) mRNA in MWCNT-treated cells and a 1.20-fold increase in SWCNT-treated cells.
  • Expression of initiator caspases (Cas8, Cas10) and other caspases (Cas4, Cas6) did not increase significantly.

Conclusions:

  • Carboxyl-functionalized CNTs, particularly MWCNTs, can up-regulate Caspase-2 (Cas2) gene expression.
  • This suggests a cell death signaling pathway initiated by carboxylated CNTs that differs from intrinsic or extrinsic apoptosis.
  • Further research is needed to elucidate the precise mechanisms of CNT-induced cytotoxicity.

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