Construction of a sensitive pyrogen-testing cell model by site-specific knock-in of multiple genes

Biotechnol Bioeng. 2019 Oct;116(10):2652-2661. doi: 10.1002/bit.27084. Epub 2019 Jul 8.

Abstract

A pyrogen test is crucial for evaluating the safety of drugs and medical equipment, especially those involved in injections. As existing pyrogen tests, including the rabbit pyrogen test, the limulus amoebocyte lysate (LAL) test and the monocyte activation test have limitations, development of new models for pyrogen testing is necessary. Here we develop a sensitive cell model for pyrogen test based on the lipopolysaccharides (LPS) signal pathway. TLR4, MD2, and CD14 play key roles in the LPS-mediated pyrogen reaction. We established a new TLR4/MD2/CD14-specific overexpressing knock-in cell model using the CRISPR/CAS9 technology and homologous recombination to detect LPS. Stimulation of our TLR4/CD14/MD2 knock-in cell line model with LPS leads to the release of the cytokines IL-6 and TNF-alpha, with a detection limit of 0.005 EU/ml, which is greatly lower than the lower limit of 0.015 EU/ml detected by the Tachypleus amebocyte lysate (TAL) assay.

Keywords: LPS signal pathway; cell model; pyrogen test; site-specific knock-in.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biosensing Techniques*
  • CRISPR-Cas Systems
  • Gene Knock-In Techniques*
  • HEK293 Cells
  • Humans
  • Lipopolysaccharide Receptors / biosynthesis
  • Lipopolysaccharide Receptors / genetics
  • Lipopolysaccharides / analysis*
  • Lymphocyte Antigen 96 / biosynthesis
  • Lymphocyte Antigen 96 / genetics
  • Models, Biological*
  • Toll-Like Receptor 4 / biosynthesis
  • Toll-Like Receptor 4 / genetics

Substances

  • CD14 protein, human
  • LY96 protein, human
  • Lipopolysaccharide Receptors
  • Lipopolysaccharides
  • Lymphocyte Antigen 96
  • TLR4 protein, human
  • Toll-Like Receptor 4

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