Preview

Fundamental and Clinical Medicine

Advanced search

Change of reception and lactate transport by cerebral endothelium under the influence of viral and bacterial inflammation in vitro

https://doi.org/10.23946/2500-0764-2020-5-1-8-14

Abstract

Aim. To study the effect of neuroinflammation inducers of viral and bacterial origin on the reception and transport of lactate in endothelial cells of the brain in vitro.

Materials and Methods. In the study, we incubated endothelial cells with bacterial inducers (lipopolysaccharide, E. coli) of various concentrations and inducer of viral inflammation (Poly I:C). After the exposure, we evaluated the proliferative activity of endothelial cells, change in transendothelial electrical resistance, and the concentration of extracellular lactate. We then performed an im-munocytochemistry investigation to record changes in the number of endothelial cells expressing the target molecules GPR81, MCT-1, IL-1β, TLR3 and ZO1.

Conclusions. Disturbance of the transport and reception of lactate can contribute to the changes in structural and functional integrity of the blood-brain barrier caused by bacterial and viral inflammation.

About the Authors

E. B. Boytsova
Voino-Yasenetskiy Krasnoyarsk State Medical University
Russian Federation

Elizaveta B. Boytsova - MD, Researcher, Mrs.

1, Partizana Zheleznyaka, Krasnoyarsk, 660022


A. V. Morgun
Voino-Yasenetskiy Krasnoyarsk State Medical University
Russian Federation

Audrey V. Morgun - MD, DSc, Researcher, Dr.

1, Partizana Zheleznyaka, Krasnoyarsk, 660022



E. D. Osipova
Voino-Yasenetskiy Krasnoyarsk State Medical University
Russian Federation

Elena D. Osipova – Researcher, Mrs.

1, Partizana Zheleznyaka, Krasnoyarsk, 660022



G. P. Martinova
Voino-Yasenetskiy Krasnoyarsk State Medical University
Russian Federation

Galina P. Martinova - MD, DSc, Prof.,Head of the Department of Pediatric Infectious Diseases.

1, Partizana Zheleznyaka, Krasnoyarsk, 660022



A. B. Salmina
Voino-Yasenetskiy Krasnoyarsk State Medical University
Russian Federation

Alla B. Salmina - MD, DSc, Prof., Senior Researcher and Head of the RIMMP, Head of the Department of Biological Chemistry, Medical, Pharmaceutical and Toxicological Chemistry, Voino-Yasenetskiy KSMU.

1, Partizana Zheleznyaka, Krasnoyarsk, 660022



References

1. Wang D, Duan H, Feng J, Xiang J, Feng L, Liu D Chen X, Jing L, Liu Z, Zhang D, Hao H, Yan X. Soluble CD146, a cerebrospinal fluid marker for neuroinflammation, promotes blood-brain barrier dysfunction. Theranostics. 2020;10(1):231-246. https://doi.org/10.7150/thno.37142

2. Lopes PC. LPS and neuroinflammation: a matter of timing. Inflammopharmacology. 2016;24(5):291-293. DOI: 10.1007/s10787-016-0283-2

3. Fortier ME, Kent S, Ashdown H, Poole S, Boksa P, Luheshi GN. The viral mimic, polyinosinic:polycytidylic acid, induces fever in rats via an interleukin-1-dependent mechanism. Am J Physiol Regul Integr Comp Physiol. 2004;287(4):R759-766. https://doi.org/10.1152/ajpregu.00293.20044

4. Perry VH. The influence of systemic inflammation on inflammation in the brain: implications for chronic neurodegenerative disease. Brain Behav Immun. 2004;18(5):407-413. https:// doi.org/10.1016/j.bbi.2004.01.004

5. Nakamura A, Osonoi T, Terauchi Y. Relationship between urinary sodium excretion and pioglitazone-induced edema. J Diabetes Investig. 2010;1(5):208-211. https://doi.org/10.1111/j.2040-1124.2010.00046.x

6. Giulieri S, Chapuis-Taillard C, Jaton K, Cometta A, Chuard C, Hugli O, Du Pasquier R, Bille J, Meylan P, Manuel O, Marchetti O. CSF lactate for accurate diagnosis of community-acquired bacterial meningitis. Eur J Clin Microbiol Infect Dis. 2015;34(10):2049-2055. https://doi.org/10.1007/s10096-015-2450-6

7. Lottes RG, Newton DA, Spyropoulos DD, Baatz JE. Lactate as substrate for mitochondrial respiration in alveolar epithelial type II cells. Am J Physiol Lung Cell Mol Physiol. 2015;308(9):L953-961. https://doi.org/10.1152/ajplung.00335.2014

8. Vegran F, Boidot R, Michiels C, Sonveaux P, Feron O. Lactate influx through the endothelial cell monocarboxylate transporter MCT1 supports an NF-kB/IL-8 pathway that drives tumor angiogenesis. Cancer Res. 2011;71(7):2550-2560. https://doi.org/10.1158/0008-5472.CAN-10-2828

9. Salmina AB, Kuvacheva NV, Morgun AV, Komleva YK, Pozhilenkova EA, Lopatina OL Gorina YV, Taranushenko TE, Petrova LL. Glycolysis-mediated control of blood-brain barrier development and function. Int J Biochem Cell Biol. 2015;64:174-184. https://doi.org/10.1016Zj.biocel.2015.04.005

10. Khilazheva ED, Pisareva NV, Morgun AV, Boitsova EB, Taranushenko TE, Frolova OV, Salmina AB. Activation of GPR81 lactate receptors stimulates mitochondrial biogenesis in cerebral microvessel endothelial cells. Ann Clin Exp Neurol. 2017;11(1):34-39. (In Russ.).

11. Liu Y, Xue Q, Tang Q, Hou M, Qi H, Chen G, Chen W, Zhang J, Chen Y, Xu X. A simple method for isolating and culturing the rat brain microvascular endothelial cells. Microvasc Res. 2013;90:199-205. https://doi.org/10.10167j.mvr.2013.08.004

12. CoisM C, Dehouck L, Faveeuw C, Delplace Y, Miller F, Landry C, Morissette C, Fenart L, Cecchelli R, Tremblay P, Dehouck B. Mouse syngenic in vitro blood-brain barrier model: a new tool to examine inflammatory events in cerebral endothelium. Lab Invest. 2005;85(6):734-746. https://doi.org/10.1038/labin-vest.3700281

13. Pan LN, Zhu W, Li C, Xu XL, Guo LJ, Lu Q. Tolllike receptor 3 agonist Poly I:C protects against simulated cerebral ischemia in vitro and in vivo. Acta Рharmacologica Sinica. 2012;33(10):1246-1253. https://doi.org/10.1038/aps.2012.122

14. Boitsova EB, Morgun AV, Osipova ED, Pozhilenkova EA, Mar-tinova GP, Frolova OV, Olovannikova RY, Tohidpour A, Gorina YV, Panina YA, Salmina AB.The inhibitory effect of LPS on the expression of GPR81 lactate receptor in blood-brain barrier model in vitro. J Neuroinflammation. 2018;15(1):196. https://doi.org/10.1186/s12974-018-1233-2


Review

For citations:


Boytsova E.B., Morgun A.V., Osipova E.D., Martinova G.P., Salmina A.B. Change of reception and lactate transport by cerebral endothelium under the influence of viral and bacterial inflammation in vitro. Fundamental and Clinical Medicine. 2020;5(1):8-14. (In Russ.) https://doi.org/10.23946/2500-0764-2020-5-1-8-14

Views: 628


Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 License.


ISSN 2500-0764 (Print)
ISSN 2542-0941 (Online)