Tracking biochemical changes correlated with ultra-weak photon emission using metabolomics

Result code in IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F67985882%3A_____%2F16%3A00469629" target="_blank" >RIV/67985882:_____/16:00469629 - isvavai.cz</a>

Alternative codes found

RIV/68407700:21230/16:00302994

Result on the web

<a href="http://dx.doi.org/10.1016/j.jphotobiol.2016.08.030" target="_blank" >http://dx.doi.org/10.1016/j.jphotobiol.2016.08.030</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1016/j.jphotobiol.2016.08.030" target="_blank" >10.1016/j.jphotobiol.2016.08.030</a>

Result language

angličtina

Original language name

Tracking biochemical changes correlated with ultra-weak photon emission using metabolomics

Original language description

Ultra-weak photon emission (UPE) is light emitted spontaneously by biological systems without the use of specific luminescent complexes. UPE is emitted in the near-UV/UV-Vis/near-IR spectra during oxidative metabolic reactions; however, the specific pathways involved in UPE remain poorly understood. Here, we used HL-60 cells, a human promyelocytic cell line that is often used to study respiratory burst, as a model system to measure UPE kinetics together with metabolic changes. HL-60 cells were differentiated into neutrophil-like cells by culturing in all-trans-retinoic acid for 7 days. We then used a targeted metabolomics approach with capillary electrophoresis-mass spectrometry to profile intracellular metabolites in HL-60 cells and to investigate the biochemical changes based on the measured UPE profile. Our analysis revealed that the levels of specific metabolites, including putrescine, creatine, beta-alanine, methionine, hydroxyproline, serine, and S-adenosylmethionine, were significantly altered in HL-60 cells after inducing respiratory burst. A comparison with recorded UPE data revealed that the changes in putrescine, glutathione, sarcosine, creatine, beta-alanine, methionine, and hydroxyproline levels were inversely correlated with the change in UPE intensity. These results suggest that these metabolic pathways, particular the methionine pathway, may play a role in the observed changes in UPE in HL-60 cells and therefore demonstrate the potential for using UPE to monitor metabolic changes

Czech name

—

Czech description

—

Type

J_x - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

CEP classification

BO - Biophysics

OECD FORD branch

—

Project

<a href="/en/project/GA13-29294S" target="_blank" >GA13-29294S: Photonic biosignals: measurement and characterization</a><br>

Continuities

I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Publication year

2016

Confidentiality

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Name of the periodical

Journal of Photochemistry and Photobiology. B - Biology Section

ISSN

1011-1344

e-ISSN

—

Volume of the periodical

—

Issue of the periodical within the volume

163

Country of publishing house

CH - SWITZERLAND

Number of pages

9

Pages from-to

237-245

UT code for WoS article

000384852000031

EID of the result in the Scopus database

2-s2.0-84984788434