In Vivo Noninvasive Monitoring of a Tissue Engineered Construct Using 1H NMR Spectroscopy

Direct, noninvasive monitoring of tissue engineered substitutes containing live, functional cells would provide valuable information on dynamic changes that occur postimplantation. Such changes include remodeling both within the construct and at the interface of the implant with the surrounding host...

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Main Authors: C. L. Stabler, R. C. Long, I. Constantinidis, A. Sambanis Ph.D.
Format: Article
Language:English
Published: SAGE Publishing 2005-02-01
Series:Cell Transplantation
Online Access:https://doi.org/10.3727/000000005783983197
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author C. L. Stabler
R. C. Long
I. Constantinidis
A. Sambanis Ph.D.
author_facet C. L. Stabler
R. C. Long
I. Constantinidis
A. Sambanis Ph.D.
author_sort C. L. Stabler
collection DOAJ
description Direct, noninvasive monitoring of tissue engineered substitutes containing live, functional cells would provide valuable information on dynamic changes that occur postimplantation. Such changes include remodeling both within the construct and at the interface of the implant with the surrounding host tissue, and may result in changes in the number of viable cells in the construct. This study investigated the use of 1H NMR spectroscopy in noninvasively monitoring the viable cell number within a tissue engineered construct in vivo. The construct consisted of mouse βTC3 insulinomas in a disk-shaped agarose gel, surrounded by a cell-free agarose gel layer. Localized 1H NMR spectra were acquired from within implanted constructs, and the total choline resonance was measured. Critical issues that had to be addressed in accurately quantifying total choline from the implanted cells included avoiding signal from host tissue and correcting for interfering signal from diffusing solutes. In vivo NMR measurements were correlated with MTT assays and NMR measurements performed in vitro on explanted constructs. Total choline measurements accurately and noninvasively quantified viable βTC3 cell numbers in vivo, in the range of 1 × 106 to more than 14 × 106 cells, and monitored changes in viable cell number that occurred in the same construct over time. This is the first study using NMR techniques to monitor viable cell numbers in an implanted tissue substitute. It established architectural characteristics that a construct should have to be amenable to NMR monitoring, and it set the foundation for future in vivo investigations with other tissue engineered implants.
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spelling doaj.art-156bcfdf5d524e94bd7b8e0a255d63fa2022-12-21T19:11:44ZengSAGE PublishingCell Transplantation0963-68971555-38922005-02-011410.3727/000000005783983197In Vivo Noninvasive Monitoring of a Tissue Engineered Construct Using 1H NMR SpectroscopyC. L. Stabler0R. C. Long1I. Constantinidis2A. Sambanis Ph.D.3Department of Biomedical Engineering, Georgia Institute of Technology/Emory University, 313 Ferst Drive, Atlanta, GA 30332-0363Fredrik Philips Magnetic Resonance Research Center, Department of Radiology, Emory University, 1639 Pierce Drive, Atlanta, GA 30322National High Magnetic Field Laboratory, 1800 E. Paul Dirac Dr., Tallahassee, FL 32310-3706School of Chemical and Biomolecular Engineering, Georgia Institute of Technology, 311 Ferst Drive, Atlanta, GA 30332-0100Direct, noninvasive monitoring of tissue engineered substitutes containing live, functional cells would provide valuable information on dynamic changes that occur postimplantation. Such changes include remodeling both within the construct and at the interface of the implant with the surrounding host tissue, and may result in changes in the number of viable cells in the construct. This study investigated the use of 1H NMR spectroscopy in noninvasively monitoring the viable cell number within a tissue engineered construct in vivo. The construct consisted of mouse βTC3 insulinomas in a disk-shaped agarose gel, surrounded by a cell-free agarose gel layer. Localized 1H NMR spectra were acquired from within implanted constructs, and the total choline resonance was measured. Critical issues that had to be addressed in accurately quantifying total choline from the implanted cells included avoiding signal from host tissue and correcting for interfering signal from diffusing solutes. In vivo NMR measurements were correlated with MTT assays and NMR measurements performed in vitro on explanted constructs. Total choline measurements accurately and noninvasively quantified viable βTC3 cell numbers in vivo, in the range of 1 × 106 to more than 14 × 106 cells, and monitored changes in viable cell number that occurred in the same construct over time. This is the first study using NMR techniques to monitor viable cell numbers in an implanted tissue substitute. It established architectural characteristics that a construct should have to be amenable to NMR monitoring, and it set the foundation for future in vivo investigations with other tissue engineered implants.https://doi.org/10.3727/000000005783983197
spellingShingle C. L. Stabler
R. C. Long
I. Constantinidis
A. Sambanis Ph.D.
In Vivo Noninvasive Monitoring of a Tissue Engineered Construct Using 1H NMR Spectroscopy
Cell Transplantation
title In Vivo Noninvasive Monitoring of a Tissue Engineered Construct Using 1H NMR Spectroscopy
title_full In Vivo Noninvasive Monitoring of a Tissue Engineered Construct Using 1H NMR Spectroscopy
title_fullStr In Vivo Noninvasive Monitoring of a Tissue Engineered Construct Using 1H NMR Spectroscopy
title_full_unstemmed In Vivo Noninvasive Monitoring of a Tissue Engineered Construct Using 1H NMR Spectroscopy
title_short In Vivo Noninvasive Monitoring of a Tissue Engineered Construct Using 1H NMR Spectroscopy
title_sort in vivo noninvasive monitoring of a tissue engineered construct using 1h nmr spectroscopy
url https://doi.org/10.3727/000000005783983197
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