ZFIN ID: ZDB-PUB-140513-491
Simultaneous Raman microspectroscopy and fluorescence imaging of bone mineralization in living zebrafish larvae
Bennet, M., Akiva, A., Faivre, D., Malkinson, G., Yaniv, K., Abdelilah-Seyfried, S., Fratzl, P., Masic, A.
Date: 2014
Source: Biophysical journal   106: L17-9 (Journal)
Registered Authors: Abdelilah-Seyfried, Salim, Malkinson, Guy, Yaniv, Karina
Keywords: none
MeSH Terms:
  • Animals
  • Calcification, Physiologic*
  • Larva/physiology
  • Microscopy, Fluorescence/methods*
  • Optical Imaging/methods*
  • Spectrum Analysis, Raman/methods*
  • Zebrafish
PubMed: 24560001 Full text @ Biophys. J.
ABSTRACT
Confocal Raman microspectroscopy and fluorescence imaging are two well-established methods providing functional insight into the extracellular matrix and into living cells and tissues, respectively, down to single molecule detection. In living tissues, however, cells and extracellular matrix coexist and interact. To acquire information on this cell-matrix interaction, we developed a technique for colocalized, correlative multispectral tissue analysis by implementing high-sensitivity, wide-field fluorescence imaging on a confocal Raman microscope. As a proof of principle, we study early stages of bone formation in the zebrafish (Danio rerio) larvae because the zebrafish has emerged as a model organism to study vertebrate development. The newly formed bones were stained using a calcium fluorescent marker and the maturation process was imaged and chemically characterized in vivo. Results obtained from early stages of mineral deposition in the zebrafish fin bone unequivocally show the presence of hydrogen phosphate containing mineral phases in addition to the carbonated apatite mineral. The approach developed here opens significant opportunities in molecular imaging of metabolic activities, intracellular sensing, and trafficking as well as in vivo exploration of cell-tissue interfaces under (patho-)physiological conditions.
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