CellNO trap: Novel device for quantitative, real-time, direct measurement of nitric oxide from cultured RAW 267.4 macrophages.

Redox Biol

Department of Biomedical Engineering, Michigan Technological University, 309 Minerals and Materials Building, 1400 Townsend Dr., Houghton, MI 49931-1295, United States. Electronic address:

Published: August 2016

AI Article Synopsis

  • - Nitric oxide (NO) is a crucial signaling molecule in biological systems that can have varying effects based on its concentration and timing of exposure, influencing both healthy and disease states.
  • - The study introduces a new measurement system called CellNO trap, which allows for real-time detection of NO from cultured cells without disrupting their function, using a specialized polymer for accurate measurements.
  • - The research demonstrates how variations in the culture conditions and the presence of stimuli (like LPS and IFN-γ) affect the production of NO in a macrophage cell line, revealing the dynamic nature of NO release and its potential implications for understanding biological responses.

Article Abstract

Nitric oxide (NO), is arguably one of the most important small signaling molecules in biological systems. It regulates various biological responses in both physiological and pathological conditions, often time producing seemingly contradictory results. The details of the effects of NO are highly dependent on the level of NO that cells experience and the temporal aspect of when and how long cells are exposed to NO. Herein, we present a novel measurement system (CellNO trap) that allows real-time NO measurement via chemiluminescence detection from general adhesive cultured cells using standard cell culture media and reagents that does not perturb the cells under investigation. Highly controlled light-initiated NO releasing polymer SNAP-PDMS was used to characterize and validate the quantitative data nature of the device. The NO generation profile from the macrophage cell-line RAW264.7 stimulated by 100ng/ml LPS and 10ng/ml IFN-γ was recorded. Measured maximum NO flux from RAW264.7 varied between around 2.5-9pmol/10(6)cell/s under 100ng/ml LPS and 10ng/ml IFN-γ stimulation, and 24h cumulative NO varied between 157 and 406 nmol/10(6)cell depending on different culture conditions, indicating the conventional report of an average flux or maximum flux is not sufficient to represent the dynamic characters of NO. LPS and IFN-γ's synergistic effect to RAW264.7 NO generation was also directly observed with the CellNO trap. The real-time effect on the NO generation from RAW264.7 following the addition of arginine, nor-NOHA and L-NAME to the cultured cells is presented. There is great potential to further our understanding of the role NO plays in normal and pathological conditions clearly understanding the dynamic production of NO in response to different stimuli and conditions; use of CellNO trap makes it possible to quantitatively determine the precise NO release profile generated from cells in a continuous and real-time manner with chemiluminescence detection.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4827804PMC
http://dx.doi.org/10.1016/j.redox.2016.03.006DOI Listing

Publication Analysis

Top Keywords

cellno trap
16
nitric oxide
8
pathological conditions
8
chemiluminescence detection
8
cultured cells
8
100ng/ml lps
8
lps 10ng/ml
8
10ng/ml ifn-γ
8
maximum flux
8
cells
6

Similar Publications

Direct measurement of actual levels of nitric oxide (NO) in cell culture conditions using soluble NO donors.

Redox Biol

October 2016

Department of Biomedical Engineering, Michigan Technological University, 309 Minerals and Materials Building, 1400 Townsend Dr., Houghton, MI 49931-1295, United States. Electronic address:

Article Synopsis
  • * To address these challenges, the researchers developed the CellNO Trap, a device that monitors the NO levels in real-time for cells in culture without altering standard culturing methods.
  • * Experiments were conducted to assess the effects of various NO donors and environmental conditions on the levels of NO experienced by murine smooth muscle cells, revealing that observed cell proliferation was more closely related to real-time NO levels than to the half-lives of the NO donors in simpler solutions.
View Article and Find Full Text PDF

CellNO trap: Novel device for quantitative, real-time, direct measurement of nitric oxide from cultured RAW 267.4 macrophages.

Redox Biol

August 2016

Department of Biomedical Engineering, Michigan Technological University, 309 Minerals and Materials Building, 1400 Townsend Dr., Houghton, MI 49931-1295, United States. Electronic address:

Article Synopsis
  • - Nitric oxide (NO) is a crucial signaling molecule in biological systems that can have varying effects based on its concentration and timing of exposure, influencing both healthy and disease states.
  • - The study introduces a new measurement system called CellNO trap, which allows for real-time detection of NO from cultured cells without disrupting their function, using a specialized polymer for accurate measurements.
  • - The research demonstrates how variations in the culture conditions and the presence of stimuli (like LPS and IFN-γ) affect the production of NO in a macrophage cell line, revealing the dynamic nature of NO release and its potential implications for understanding biological responses.
View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!