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Hydrogel-Mediated Release of TRPV1 Modulators to Fine Tune Osteoclastogenesis

[Image: see text] Bone defects, including bone loss due to increased osteoclast activity, have become a global health-related issue. Osteoclasts attach to the bone matrix and resorb the same, playing a vital role in bone remodeling. Ca(2+) homeostasis plays a pivotal role in the differentiation and...

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Autores principales: Chakraborty, Ranabir, Acharya, Tusar Kanta, Tiwari, Nikhil, Majhi, Rakesh Kumar, Kumar, Satish, Goswami, Luna, Goswami, Chandan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8945112/
https://www.ncbi.nlm.nih.gov/pubmed/35350319
http://dx.doi.org/10.1021/acsomega.1c06915
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author Chakraborty, Ranabir
Acharya, Tusar Kanta
Tiwari, Nikhil
Majhi, Rakesh Kumar
Kumar, Satish
Goswami, Luna
Goswami, Chandan
author_facet Chakraborty, Ranabir
Acharya, Tusar Kanta
Tiwari, Nikhil
Majhi, Rakesh Kumar
Kumar, Satish
Goswami, Luna
Goswami, Chandan
author_sort Chakraborty, Ranabir
collection PubMed
description [Image: see text] Bone defects, including bone loss due to increased osteoclast activity, have become a global health-related issue. Osteoclasts attach to the bone matrix and resorb the same, playing a vital role in bone remodeling. Ca(2+) homeostasis plays a pivotal role in the differentiation and maturation of osteoclasts. In this work, we examined the role of TRPV1, a nonselective cation channel, in osteoclast function and differentiation. We demonstrate that endogenous TRPV1 is functional and causes Ca(2+) influx upon activation with pharmacological activators [resiniferatoxin (RTX) and capsaicin] at nanomolar concentration, which enhances the generation of osteoclasts, whereas the TRPV1 inhibitor (5′-IRTX) reduces osteoclast differentiation. Activation of TRPV1 upregulates tartrate-resistant acid phosphatase activity and the expression of cathepsin K and calcitonin receptor genes, whereas TRPV1 inhibition reverses this effect. The slow release of capsaicin or RTX at a nanomolar concentration from a polysaccharide-based hydrogel enhances bone marrow macrophage (BMM) differentiation into osteoclasts whereas release of 5′-IRTX, an inhibitor of TRPV1, prevents macrophage fusion and osteoclast formation. We also characterize several subcellular parameters, including reactive oxygen (ROS) and nitrogen (RNS) species in the cytosol, mitochondrial, and lysosomal profiles in BMMs. ROS were found to be unaltered upon TRPV1 modulation. NO, however, had elevated levels upon RTX-mediated TRPV1 activation. Capsaicin altered mitochondrial membrane potential (ΔΨm) of BMMs but not 5′-IRTX. Channel modulation had no significant impact on cytosolic pH but significantly altered the pH of lysosomes, making these organelles less acidic. Since BMMs are precursors for osteoclasts, our findings of the cellular physiology of these cells may have broad implications in understanding the role of thermosensitive ion channels in bone formation and functions, and the TRPV1 modulator-releasing hydrogel may have application in bone tissue engineering and other biomedical sectors.
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spelling pubmed-89451122022-03-28 Hydrogel-Mediated Release of TRPV1 Modulators to Fine Tune Osteoclastogenesis Chakraborty, Ranabir Acharya, Tusar Kanta Tiwari, Nikhil Majhi, Rakesh Kumar Kumar, Satish Goswami, Luna Goswami, Chandan ACS Omega [Image: see text] Bone defects, including bone loss due to increased osteoclast activity, have become a global health-related issue. Osteoclasts attach to the bone matrix and resorb the same, playing a vital role in bone remodeling. Ca(2+) homeostasis plays a pivotal role in the differentiation and maturation of osteoclasts. In this work, we examined the role of TRPV1, a nonselective cation channel, in osteoclast function and differentiation. We demonstrate that endogenous TRPV1 is functional and causes Ca(2+) influx upon activation with pharmacological activators [resiniferatoxin (RTX) and capsaicin] at nanomolar concentration, which enhances the generation of osteoclasts, whereas the TRPV1 inhibitor (5′-IRTX) reduces osteoclast differentiation. Activation of TRPV1 upregulates tartrate-resistant acid phosphatase activity and the expression of cathepsin K and calcitonin receptor genes, whereas TRPV1 inhibition reverses this effect. The slow release of capsaicin or RTX at a nanomolar concentration from a polysaccharide-based hydrogel enhances bone marrow macrophage (BMM) differentiation into osteoclasts whereas release of 5′-IRTX, an inhibitor of TRPV1, prevents macrophage fusion and osteoclast formation. We also characterize several subcellular parameters, including reactive oxygen (ROS) and nitrogen (RNS) species in the cytosol, mitochondrial, and lysosomal profiles in BMMs. ROS were found to be unaltered upon TRPV1 modulation. NO, however, had elevated levels upon RTX-mediated TRPV1 activation. Capsaicin altered mitochondrial membrane potential (ΔΨm) of BMMs but not 5′-IRTX. Channel modulation had no significant impact on cytosolic pH but significantly altered the pH of lysosomes, making these organelles less acidic. Since BMMs are precursors for osteoclasts, our findings of the cellular physiology of these cells may have broad implications in understanding the role of thermosensitive ion channels in bone formation and functions, and the TRPV1 modulator-releasing hydrogel may have application in bone tissue engineering and other biomedical sectors. American Chemical Society 2022-03-09 /pmc/articles/PMC8945112/ /pubmed/35350319 http://dx.doi.org/10.1021/acsomega.1c06915 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Chakraborty, Ranabir
Acharya, Tusar Kanta
Tiwari, Nikhil
Majhi, Rakesh Kumar
Kumar, Satish
Goswami, Luna
Goswami, Chandan
Hydrogel-Mediated Release of TRPV1 Modulators to Fine Tune Osteoclastogenesis
title Hydrogel-Mediated Release of TRPV1 Modulators to Fine Tune Osteoclastogenesis
title_full Hydrogel-Mediated Release of TRPV1 Modulators to Fine Tune Osteoclastogenesis
title_fullStr Hydrogel-Mediated Release of TRPV1 Modulators to Fine Tune Osteoclastogenesis
title_full_unstemmed Hydrogel-Mediated Release of TRPV1 Modulators to Fine Tune Osteoclastogenesis
title_short Hydrogel-Mediated Release of TRPV1 Modulators to Fine Tune Osteoclastogenesis
title_sort hydrogel-mediated release of trpv1 modulators to fine tune osteoclastogenesis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8945112/
https://www.ncbi.nlm.nih.gov/pubmed/35350319
http://dx.doi.org/10.1021/acsomega.1c06915
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