Tracking protein function with sodium multi quantum spectroscopy in a 3D-tissue culture based on microcavity arrays
Abstract:
The aim of this study was to observe the effects of strophanthin induced inhibition of the Na-/KATPase
in liver cells using a magnetic resonance (MR) compatible bioreactor. A microcavity array with
a high density three-dimensional cell culture served as a functional magnetic resonance imaging (MRI)
phantom for sodium multi quantum (MQ) spectroscopy. Direct contrast enhanced (DCE) MRI revealed
the homogenous distribution of biochemical substances inside the bioreactor. NMR experiments using
advanced bioreactors have advantages with respect to having full control over a variety of physiological
parameters such as temperature, gas composition and fluid flow. Simultaneous detection of single
quantum (SQ) and triple quantum (TQ) MR signals improves accuracy and was achieved by application
of a pulse sequence with a time proportional phase increment (TQTPPI). The time course of the Na-/KATPase
inhibition in the cell culture was demonstrated by the corresponding alterations of sodium TQ/
SQ MR signals.
in liver cells using a magnetic resonance (MR) compatible bioreactor. A microcavity array with
a high density three-dimensional cell culture served as a functional magnetic resonance imaging (MRI)
phantom for sodium multi quantum (MQ) spectroscopy. Direct contrast enhanced (DCE) MRI revealed
the homogenous distribution of biochemical substances inside the bioreactor. NMR experiments using
advanced bioreactors have advantages with respect to having full control over a variety of physiological
parameters such as temperature, gas composition and fluid flow. Simultaneous detection of single
quantum (SQ) and triple quantum (TQ) MR signals improves accuracy and was achieved by application
of a pulse sequence with a time proportional phase increment (TQTPPI). The time course of the Na-/KATPase
inhibition in the cell culture was demonstrated by the corresponding alterations of sodium TQ/
SQ MR signals.
| Zugehörige Institution(en) am KIT | Institut für Biologische Grenzflächen (IBG) Institut für Funktionelle Grenzflächen (IFG) |
| Publikationstyp | Zeitschriftenaufsatz |
| Publikationsjahr | 2017 |
| Sprache | Englisch |
| Identifikator | ISSN: 2045-2322 urn:nbn:de:swb:90-717915 KITopen-ID: 1000071791 |
| HGF-Programm | 47.02.05 (POF III, LK 01) Zellpopul.auf Biofunk.Oberflächen IBG-5 |
| Erschienen in | Scientific reports |
| Verlag | Nature Research |
| Band | 7 |
| Seiten | Art. Nr. 3943 |
| Vorab online veröffentlicht am | 21.06.2017 |
| Nachgewiesen in | Web of Science Scopus Dimensions |