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Improving the visualization of fluorescently tagged nanoparticles and fluorophore-labeled molecular probes by treatment with CuSO(4) to quench autofluorescence in the rat inner ear

Improving the visualization of fluorescently tagged nanoparticles and fluorophore-labeled molecular probes by treatment with CuSO(4) to quench autofluorescence in the rat inner ear
Improving the visualization of fluorescently tagged nanoparticles and fluorophore-labeled molecular probes by treatment with CuSO(4) to quench autofluorescence in the rat inner ear
Fluorescent tags and fluorophore-conjugated molecular probes have been extensively employed in histological studies to demonstrate nanoparticle distribution in inner ear cell populations. However, autofluorescence that exists in the rodent cochleae disturbs visualization of the fluorescent tags and fluorophore labeling.

In the present work, we aimed to improve the visualization of fluorescently tagged nanoparticles and fluorophore-labeled molecular probes by treatment with CuSO4 to quench autofluorescence in the rat inner ear. The in vivo study was performed on eight- to nine-month-old rats using confocal laser scanning microscopy, and the in vitro study was carried out with DiI-tagged poly(ethylene glycol) and poly(capro-lactone) polymersomes and different fluorescent-labeling agents using a spectrofluorometer. The nanoparticles were intratympanically administered using either an osmotic pump or transtympanic injection.

Abundant autofluorescence was detected in spiral ganglion cells (SGCs), stria marginal cells, spiral ligament fibrocytes (SL) and the subcuticular cytoplasm of inner hair cells (IHCs). Sparsely distributed faint autofluorescence was also visualized in outer hair cells (OHCs). The autofluorescence was eliminated by treatment with 1 mM CuSO4 (in 0.01 M ammonium acetate buffer) for 70–90 min, while the fluorescent tag in the nanoparticle was absolutely preserved and the labeling fluorescence signals of the molecular probes were mostly retained.
0378-5955
1-11
Zhang, Ya
1820fb16-8a49-4749-9964-12bcbded2641
Zhang, Weikai
d742f246-a5f8-4b4f-b249-7676d4769fa7
Johnston, Alexander H.
b3325b84-67c4-4d9c-ba97-57f2fdf017ba
Newman, Tracey A.
322290cb-2e9c-445d-a047-00b1bea39a25
Pyykko, Iimari
5c1ca702-cb89-46c5-adf8-e4a34cfb7dd3
Zou, Jing
00c594ea-0fc7-447c-88af-014ee31f1454
Zhang, Ya
1820fb16-8a49-4749-9964-12bcbded2641
Zhang, Weikai
d742f246-a5f8-4b4f-b249-7676d4769fa7
Johnston, Alexander H.
b3325b84-67c4-4d9c-ba97-57f2fdf017ba
Newman, Tracey A.
322290cb-2e9c-445d-a047-00b1bea39a25
Pyykko, Iimari
5c1ca702-cb89-46c5-adf8-e4a34cfb7dd3
Zou, Jing
00c594ea-0fc7-447c-88af-014ee31f1454

Zhang, Ya, Zhang, Weikai, Johnston, Alexander H., Newman, Tracey A., Pyykko, Iimari and Zou, Jing (2010) Improving the visualization of fluorescently tagged nanoparticles and fluorophore-labeled molecular probes by treatment with CuSO(4) to quench autofluorescence in the rat inner ear. Hearing Research, 269 (1-2), 1-11. (doi:10.1016/j.heares.2010.07.006). (PMID:20659540)

Record type: Article

Abstract

Fluorescent tags and fluorophore-conjugated molecular probes have been extensively employed in histological studies to demonstrate nanoparticle distribution in inner ear cell populations. However, autofluorescence that exists in the rodent cochleae disturbs visualization of the fluorescent tags and fluorophore labeling.

In the present work, we aimed to improve the visualization of fluorescently tagged nanoparticles and fluorophore-labeled molecular probes by treatment with CuSO4 to quench autofluorescence in the rat inner ear. The in vivo study was performed on eight- to nine-month-old rats using confocal laser scanning microscopy, and the in vitro study was carried out with DiI-tagged poly(ethylene glycol) and poly(capro-lactone) polymersomes and different fluorescent-labeling agents using a spectrofluorometer. The nanoparticles were intratympanically administered using either an osmotic pump or transtympanic injection.

Abundant autofluorescence was detected in spiral ganglion cells (SGCs), stria marginal cells, spiral ligament fibrocytes (SL) and the subcuticular cytoplasm of inner hair cells (IHCs). Sparsely distributed faint autofluorescence was also visualized in outer hair cells (OHCs). The autofluorescence was eliminated by treatment with 1 mM CuSO4 (in 0.01 M ammonium acetate buffer) for 70–90 min, while the fluorescent tag in the nanoparticle was absolutely preserved and the labeling fluorescence signals of the molecular probes were mostly retained.

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More information

e-pub ahead of print date: 24 July 2010
Published date: 1 October 2010
Organisations: Clinical Neurosciences

Identifiers

Local EPrints ID: 163115
URI: http://eprints.soton.ac.uk/id/eprint/163115
ISSN: 0378-5955
PURE UUID: 39717b12-b49b-448b-8eb9-1c289cac6226
ORCID for Tracey A. Newman: ORCID iD orcid.org/0000-0002-3727-9258

Catalogue record

Date deposited: 03 Sep 2010 10:00
Last modified: 14 Mar 2024 02:39

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Contributors

Author: Ya Zhang
Author: Weikai Zhang
Author: Alexander H. Johnston
Author: Iimari Pyykko
Author: Jing Zou

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