» Articles » PMID: 37108162

Construction of Bone Hypoxic Microenvironment Based on Bone-on-a-Chip Platforms

Overview
Journal Int J Mol Sci
Publisher MDPI
Date 2023 Apr 28
PMID 37108162
Authors
Affiliations
Soon will be listed here.
Abstract

The normal physiological activities and functions of bone cells cannot be separated from the balance of the oxygenation level, and the physiological activities of bone cells are different under different oxygenation levels. At present, in vitro cell cultures are generally performed in a normoxic environment, and the partial pressure of oxygen of a conventional incubator is generally set at 141 mmHg (18.6%, close to the 20.1% oxygen in ambient air). This value is higher than the mean value of the oxygen partial pressure in human bone tissue. Additionally, the further away from the endosteal sinusoids, the lower the oxygen content. It follows that the construction of a hypoxic microenvironment is the key point of in vitro experimental investigation. However, current methods of cellular research cannot realize precise control of oxygenation levels at the microscale, and the development of microfluidic platforms can overcome the inherent limitations of these methods. In addition to discussing the characteristics of the hypoxic microenvironment in bone tissue, this review will discuss various methods of constructing oxygen gradients in vitro and measuring oxygen tension from the microscale based on microfluidic technology. This integration of advantages and disadvantages to perfect the experimental study will help us to study the physiological responses of cells under more physiological-relevant conditions and provide a new strategy for future research on various in vitro cell biomedicines.

Citing Articles

Nanoparticles and bone microenvironment: a comprehensive review for malignant bone tumor diagnosis and treatment.

Guan Y, Zhang W, Mao Y, Li S Mol Cancer. 2024; 23(1):246.

PMID: 39487487 PMC: 11529338. DOI: 10.1186/s12943-024-02161-1.


Tumor-on-chip platforms for breast cancer continuum concept modeling.

Neagu A, Whitham D, Bruno P, Versaci N, Biggers P, Darie C Front Bioeng Biotechnol. 2024; 12:1436393.

PMID: 39416279 PMC: 11480020. DOI: 10.3389/fbioe.2024.1436393.


Differential but complementary roles of HIF-1α and HIF-2α in the regulation of bone homeostasis.

Lee S, Kim S, Park K, Lee G, Oh Y, Ryu J Commun Biol. 2024; 7(1):892.

PMID: 39039245 PMC: 11263705. DOI: 10.1038/s42003-024-06581-z.


Advances in Red Blood Cells Research.

Bogdanova A, Kaestner L Cells. 2024; 13(4.

PMID: 38391972 PMC: 10887574. DOI: 10.3390/cells13040359.

References
1.
Kan C, Lu X, Zhang R . Effects of hypoxia on bone metabolism and anemia in patients with chronic kidney disease. World J Clin Cases. 2022; 9(34):10616-10625. PMC: 8686129. DOI: 10.12998/wjcc.v9.i34.10616. View

2.
Melnikov P, Alexandrovskaya A, Naumova A, Arlyapov V, Kamanina O, Popova N . Optical Oxygen Sensing and Clark Electrode: Face-to-Face in a Biosensor Case Study. Sensors (Basel). 2022; 22(19). PMC: 9572888. DOI: 10.3390/s22197626. View

3.
Wu L, Chen Y, Chen Y, Yang W, Han Y, Lu L . Effect of HIF-1α/miR-10b-5p/PTEN on Hypoxia-Induced Cardiomyocyte Apoptosis. J Am Heart Assoc. 2019; 8(18):e011948. PMC: 6818010. DOI: 10.1161/JAHA.119.011948. View

4.
Kim E, Yoo Y, Yang W, Lim Y, Na T, Lee I . Transcriptional activation of HIF-1 by RORalpha and its role in hypoxia signaling. Arterioscler Thromb Vasc Biol. 2008; 28(10):1796-802. DOI: 10.1161/ATVBAHA.108.171546. View

5.
Wan C, Shao J, Gilbert S, Riddle R, Long F, Johnson R . Role of HIF-1alpha in skeletal development. Ann N Y Acad Sci. 2010; 1192:322-6. PMC: 3047468. DOI: 10.1111/j.1749-6632.2009.05238.x. View