Abstract

Osteoblastic mineralization occurs during the early stages of bone formation. During this mineralization, hydroxyapatite (HA), a major component of bone, is synthesized, generating hard tissue. Many of the mechanisms driving biomineralization remain unclear because the traditional biochemical assays used to investigate them are destructive techniques incompatible with viable cells. To determine the temporal changes in mineralization-related biomolecules at mineralization spots, we performed time-lapse Raman imaging of mouse osteoblasts at a subcellular resolution throughout the mineralization process. Raman imaging enabled us to analyze the dynamics of the related biomolecules at mineralization spots throughout the entire process of mineralization. Here, we stimulated KUSA-A1 cells to differentiate into osteoblasts and conducted time-lapse Raman imaging on them every 4 hours for 24 hours, beginning 5 days after the stimulation. The HA and cytochrome c Raman bands were used as markers for osteoblastic mineralization and apoptosis. From the Raman images successfully acquired throughout the mineralization process, we found that β-carotene acts as a biomarker that indicates the initiation of osteoblastic mineralization. A fluctuation of cytochrome c concentration, which indicates cell apoptosis, was also observed during mineralization. We expect time-lapse Raman imaging to help us to further elucidate osteoblastic mineralization mechanisms that have previously been unobservable.

Highlights

  • Osteoblastic mineralization begins with the differentiation of mesenchymal stem cells (MSCs) into osteoblasts

  • We report here the longitudinal time-lapse Raman imaging analysis of individual osteoblasts throughout the process of mineralization

  • Our results suggest that β -carotene was used as a biomarker to indicate the initiation of osteoblastic mineralization

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Summary

Introduction

Osteoblastic mineralization begins with the differentiation of mesenchymal stem cells (MSCs) into osteoblasts. The intensity of spontaneous Raman scattering from sample molecules is typically weak because only a tiny amount of scattered photons, approximately 1 in 10 million, has a different frequency than the incident light, when the frequency of the incident light is close to the electronic transition energy of a specific molecule, the Raman scattering intensity from that molecular species greatly increases. This phenomenon, known as resonance Raman scattering, has an intensity about 103–105 times larger than the spontaneous Raman intensity. Okada et al monitored the release of cytochrome c from mitochondria during stimulation of the apoptosis pathways by detecting the resonance Raman signal from cytochrome c at an excitation wavelength of 532 nm

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