Hydrogel-Mediated Release of TRPV1 Modulators to Fine Tune Osteoclastogenesis

Ranabir Chakraborty; Tusar Kanta Acharya; Nikhil Tiwari; Rakesh Kumar Majhi; Satish Kumar; Luna Goswami; Chandan Goswami

doi:10.1021/acsomega.1c06915

Hydrogel-Mediated Release of TRPV1 Modulators to Fine Tune Osteoclastogenesis

ACS Omega. 2022 Mar 9;7(11):9537-9550. doi: 10.1021/acsomega.1c06915. eCollection 2022 Mar 22.

Authors

Ranabir Chakraborty¹, Tusar Kanta Acharya^{1

2}, Nikhil Tiwari^{1

2}, Rakesh Kumar Majhi^{1

2}, Satish Kumar³, Luna Goswami^{3

4}, Chandan Goswami^{1

2}

Affiliations

¹ School of Biological Sciences, National Institute of Science Education and Research Bhubaneswar, P.O. Jatni, Khurda, Odisha 752050, India.
² Homi Bhabha National Institute, Training School Complex, Anushakti Nagar, Mumbai 400094, India.
³ School of Biotechnology, Kalinga Institute of Industrial Technology (KIIT), Deemed to be University, Bhubaneswar, Odisha 751024, India.
⁴ School of Chemical Technology, Kalinga Institute of Industrial Technology (KIIT), Deemed to be University, Bhubaneswar, Odisha 751024, India.

Abstract

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. Ca²⁺ 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 Ca²⁺ 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.