» Articles » PMID: 28542339

Bioenergetic Profile of Human Coronary Artery Smooth Muscle Cells and Effect of Metabolic Intervention

Overview
Journal PLoS One
Date 2017 May 26
PMID 28542339
Citations 18
Authors
Affiliations
Soon will be listed here.
Abstract

Bioenergetics of artery smooth muscle cells is critical in cardiovascular health and disease. An acute rise in metabolic demand causes vasodilation in systemic circulation while a chronic shift in bioenergetic profile may lead to vascular diseases. A decrease in intracellular ATP level may trigger physiological responses while dedifferentiation of contractile smooth muscle cells to a proliferative and migratory phenotype is often observed during pathological processes. Although it is now possible to dissect multiple building blocks of bioenergetic components quantitatively, detailed cellular bioenergetics of artery smooth muscle cells is still largely unknown. Thus, we profiled cellular bioenergetics of human coronary artery smooth muscle cells and effects of metabolic intervention. Mitochondria and glycolysis stress tests utilizing Seahorse technology revealed that mitochondrial oxidative phosphorylation accounted for 54.5% of ATP production at rest with the remaining 45.5% due to glycolysis. Stress tests also showed that oxidative phosphorylation and glycolysis can increase to a maximum of 3.5 fold and 1.25 fold, respectively, indicating that the former has a high reserve capacity. Analysis of bioenergetic profile indicated that aging cells have lower resting oxidative phosphorylation and reduced reserve capacity. Intracellular ATP level of a single cell was estimated to be over 1.1 mM. Application of metabolic modulators caused significant changes in mitochondria membrane potential, intracellular ATP level and ATP:ADP ratio. The detailed breakdown of cellular bioenergetics showed that proliferating human coronary artery smooth muscle cells rely more or less equally on oxidative phosphorylation and glycolysis at rest. These cells have high respiratory reserve capacity and low glycolysis reserve capacity. Metabolic intervention influences both intracellular ATP concentration and ATP:ADP ratio, where subtler changes may be detected by the latter.

Citing Articles

Tracking fructose 1,6-bisphosphate dynamics in liver cancer cells using a fluorescent biosensor.

Perez-Chavez I, Koberstein J, Malo Pueyo J, Gilglioni E, Vertommen D, Baeyens N iScience. 2024; 27(12):111336.

PMID: 39640569 PMC: 11617404. DOI: 10.1016/j.isci.2024.111336.


Variable bioenergetic sensitivity of neurons and astrocytes to insulin and extracellular glucose.

Sims S, Frazier H, Case S, Lin R, Trosper J, Vekaria H NPJ Metab Health Dis. 2024; 2(1):33.

PMID: 39524535 PMC: 11549053. DOI: 10.1038/s44324-024-00037-y.


The Role of Mitochondrial Dysfunction in CKD-Related Vascular Calcification: From Mechanisms to Therapeutics.

Huang J, Hao J, Wang P, Xu Y Kidney Int Rep. 2024; 9(9):2596-2607.

PMID: 39291213 PMC: 11403042. DOI: 10.1016/j.ekir.2024.05.005.


Addressing Cardiovascular Toxicity Risk of Electronic Nicotine Delivery Systems in the Twenty-First Century: "What Are the Tools Needed for the Job?" and "Do We Have Them?".

Chandy M, Hill 3rd T, Jimenez-Tellez N, Wu J, Sarles S, Hensel E Cardiovasc Toxicol. 2024; 24(5):435-471.

PMID: 38555547 PMC: 11485265. DOI: 10.1007/s12012-024-09850-9.


Wnt16 Promotes Vascular Smooth Muscle Contractile Phenotype and Function via Taz (Wwtr1) Activation in Male LDLR-/- Mice.

Behrmann A, Zhong D, Li L, Xie S, Mead M, Sabaeifard P Endocrinology. 2023; 165(2).

PMID: 38123514 PMC: 10765280. DOI: 10.1210/endocr/bqad192.


References
1.
Dranka B, Benavides G, Diers A, Giordano S, Zelickson B, Reily C . Assessing bioenergetic function in response to oxidative stress by metabolic profiling. Free Radic Biol Med. 2011; 51(9):1621-35. PMC: 3548422. DOI: 10.1016/j.freeradbiomed.2011.08.005. View

2.
Flagg T, Enkvetchakul D, Koster J, Nichols C . Muscle KATP channels: recent insights to energy sensing and myoprotection. Physiol Rev. 2010; 90(3):799-829. PMC: 3125986. DOI: 10.1152/physrev.00027.2009. View

3.
Berg J, Hung Y, Yellen G . A genetically encoded fluorescent reporter of ATP:ADP ratio. Nat Methods. 2009; 6(2):161-6. PMC: 2633436. DOI: 10.1038/nmeth.1288. View

4.
Paul R . Functional compartmentalization of oxidative and glycolytic metabolism in vascular smooth muscle. Am J Physiol. 1983; 244(5):C399-409. DOI: 10.1152/ajpcell.1983.244.5.C399. View

5.
Pung Y, Sam W, Hardwick J, Yin L, Ohanyan V, Logan S . The role of mitochondrial bioenergetics and reactive oxygen species in coronary collateral growth. Am J Physiol Heart Circ Physiol. 2013; 305(9):H1275-80. PMC: 3840244. DOI: 10.1152/ajpheart.00077.2013. View