Scientists in Japan develop novel microscopy to analyze oxygenation within living murine bone tissue, with implications for bone resorption
Without doubt, the future of life sciences is sure to have technology that can measure biological parameters real-time in living organisms. This would definitely help monitor tissue homeostasis, on the go. One important component of such homeostasis is the tissue oxygen concentration.
Under normoxic conditions, the tissues have enough oxygen for the upkeep of biological functions. But in hypoxic conditions—the state of oxygen deprivation inducible in real life during travels at high altitudes or through asphyxiation—the tissue may not have enough oxygen for such upkeep. This triggers a hypoxic response. The cells involved are likely to activate mechanisms that ensure hypoxia mitigation.
To explore further the intricacies of cellular response to variable oxygen concentrations in the living body, as a first futuristic step, scientists have successfully developed an advanced imaging technique involving two-photon phosphorescence lifetime imaging microscopy. They applied this microscopy technique in live mice to measure oxygen concentration in situ within multinucleated giant cells called osteoclasts that facilitate bone resorption. Their findings have been published as a research article in EMBO Reports.
The lead author of the study, explains the motivation behind their research, thus: “Through this study, we suggest a new approach to understand the physiological mechanisms of living organisms by accurately measuring the concentration of biomolecules deep in biological tissues. We believe ours is the first quantitative research attempt in the life sciences, similar to the that applied in the physical and chemical sciences to understand natural phenomena mathematically.”
Accordingly, through their work, the scientists were able to determine the physiological range of oxygen tension within osteoclasts of live mice, which they note to be from 17.4 to 36.4 mmHg, under hypoxic and normoxic conditions, respectively. This means that physiological normoxia corresponds to 5% and hypoxia to 2% oxygen in osteoclasts.
Also, their independent analysis of hypoxic conditions in bone tissue showed that the dearth of oxygen severely limits osteoclastogenesis or the process by which new osteoclasts grow. Further, they were able to identify that hypoxia interferes with the activity of ten-eleven translocation (TET) enzymes, which play a vital role in osteoclastogenesis through oxygen-dependent DNA methylation. Mechanistically, Tet2/3 cooperatively induces Prdm1 expression via oxygen-dependent DNA demethylation, which in turn activates NFATc1 required for osteoclastogenesis. Thus, the scientists suggest that osteoclastogenesis may be limited independent of energy metabolism and hypoxia-inducible factor activity under conditions of 2% oxygen in osteoclasts.
Overall, the study has not only put forth a novel imaging technique to measure oxygen concentration but has also deciphered a key molecular mechanism involved in osteoclastogenesis. The importance of TET enzymes in regulating osteoclastogenesis within the physiological range of oxygen tension may help unravel hitherto unreported mechanisms of physiological response to oxygen perturbation.
https://www.embopress.org/doi/full/10.15252/embr.202153035
http://sciencemission.com/site/index.php?page=news&type=view&id=publications%2Fosteoclasts-adapt-to&filter=22
Imaging epigenetic mechanisms that help bone resorbing cells handle oxygen stress
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