bioRxiv Science⌕ Search

Biology subjects

Katsamenis, O. L.

Publications and source records attributed to Katsamenis, O. L..

2 recordsLinked to original sources

In vivo X-ray Computed Microtomography: A Novel Approach to Assess Coral Skeletal Construction

Scleractinian (stony) corals build reef frameworks through calcium carbonate deposition, yet all methods for assessing skeletal growth - staining, SEM, or ex vivo {micro}CT - are limited to endpoint measurements on dead specimens. Here, we utilise in vivo X-ray computed microtomography ({micro}CT) to non-destructively quantify skeletal growth in the reef-building coral Stylophora pistillata for the first time. Our in vivo {micro}CT approach applied to one individual over 16 days revealed a volume increase from [~]630 to [~]700 mm3 that can be partitioned into external vertical extension and internal lateral thickening, generating high-resolution 4D reconstructions of the evolving skeletal architecture. These measurements were consistent with established approaches but provide additional unique insights into internal growth dynamics. We demonstrate that in vivo CT enables micron-scale monitoring of calcification processes of living stony corals, thereby representing a powerful new tool to probe coral growth dynamics in the face of rapidly changing environmental conditions.

bioengineering↗

68Ga-Bisphosphonates for the Imaging of Extraosseous Calcification by Positron Emission Tomography

Radiolabelled bisphosphonates (BPs) and [18F]NaF (18F-fluoride) are the two types of radiotracers available to image calcium mineral in vivo (e.g. bone), yet only [18F]NaF has been widely explored for the non-invasive molecular imaging of extraosseous calcification (EC) using the highly sensitive nuclear imaging technique positron emission tomography (PET). These two radiotracers bind calcium mineral deposits via different mechanisms, with BPs chelating to calcium ions and thus being non-selective, and [18F]NaF being selective for hydroxyapatite (HAp) which is the main component of bone mineral. Taking into account that the composition of EC has been reported to include a diverse range of non-HAp calcium minerals, we hypothesised that BPs may be more sensitive for imaging EC due to their ability to bind to both HAp and non-HAp deposits. To test this hypothesis, we report a comparison between the 68Ga-labelled BP tracer [68Ga]Ga-THP-Pam and [18F]NaF for PET imaging in a rat model of EC that develops macro- and microcalcifications in several organs. The presence of macrocalcifications was identified using preclinical computed tomography (CT) and microcalcifications were identified using CT-based 3D X-ray histology (XRH) on isolated organs ex vivo. The morphological and mineral analysis of individual calcified deposits was performed using scanning electron microscopy (SEM) and energy-dispersive X-ray spectroscopy (EDX). The PET imaging and ex vivo analysis results demonstrated that while both radiotracers behave similarly for bone imaging, the BP-based radiotracer [68Ga]Ga-THP-Pam was able to detect EC more sensitively in several organs in which the mineral composition departs from that of HAp. We conclude that BP-based PET radiotracers such as [68Ga]Ga-THP-Pam have a particular advantage for the sensitive imaging and early detection of EC by being able to detect a wider array of relevant calcium minerals in vivo than [18F]NaF, and should be evaluated clinically for this purpose.

pharmacology and toxicology↗