Two-Photon Excited Fluorescence Lifetime Imaging of Tetracycline-Labeled Retinal Calcification.

FLIM FLIO age-related macular degeneration calcification chlortetracycline doxycycline drusen fluorescence lifetime imaging hydroxyapatite retina whitlockite

Journal

Sensors (Basel, Switzerland)
ISSN: 1424-8220
Titre abrégé: Sensors (Basel)
Pays: Switzerland
ID NLM: 101204366

Informations de publication

Date de publication:
24 Jul 2023
Historique:
received: 07 04 2023
revised: 14 06 2023
accepted: 19 07 2023
medline: 31 7 2023
pubmed: 29 7 2023
entrez: 29 7 2023
Statut: epublish

Résumé

Deposition of calcium-containing minerals such as hydroxyapatite and whitlockite in the subretinal pigment epithelial (sub-RPE) space of the retina is linked to the development of and progression to the end-stage of age-related macular degeneration (AMD). AMD is the most common eye disease causing blindness amongst the elderly in developed countries; early diagnosis is desirable, particularly to begin treatment where available. Calcification in the sub-RPE space is also directly linked to other diseases such as Pseudoxanthoma elasticum (PXE). We found that these mineral deposits could be imaged by fluorescence using tetracycline antibiotics as specific stains. Binding of tetracyclines to the minerals was accompanied by increases in fluorescence intensity and fluorescence lifetime. The lifetimes for tetracyclines differed substantially from the known background lifetime of the existing natural retinal fluorophores, suggesting that calcification could be visualized by lifetime imaging. However, the excitation wavelengths used to excite these lifetime changes were generally shorter than those approved for retinal imaging. Here, we show that tetracycline-stained drusen in

Identifiants

pubmed: 37514920
pii: s23146626
doi: 10.3390/s23146626
pmc: PMC10386431
pii:
doi:

Substances chimiques

Tetracycline F8VB5M810T
Anti-Bacterial Agents 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NIA NIH HHS
ID : P01 AG081167
Pays : United States
Organisme : NEI NIH HHS
ID : R01 EY 030443
Pays : United States
Organisme : NEI NIH HHS
ID : R01 EY030443
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI172487
Pays : United States
Organisme : NIA NIH HHS
ID : NIA 030443-03S1
Pays : United States

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Auteurs

Kavita R Hegde (KR)

Department of Natural Sciences, Coppin State University, Baltimore, MD 21216, USA.

Krishanu Ray (K)

Department of Biochemistry and Molecular Biology, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
Institute of Human Virology, University of Maryland School of Medicine, Baltimore, MD 21201, USA.

Henryk Szmacinski (H)

Department of Biochemistry and Molecular Biology, University of Maryland School of Medicine, Baltimore, MD 21201, USA.

Sharon Sorto (S)

Department of Neurobiology, University of Maryland School of Medicine, Baltimore, MD 21201, USA.

Adam C Puche (AC)

Department of Neurobiology, University of Maryland School of Medicine, Baltimore, MD 21201, USA.

Imre Lengyel (I)

The Wellcome-Wolfson Institute for Experimental Medicine, School of Medicine, Dentistry and Biomedical Science, Queen's University Belfast, Belfast BT9 7BL, UK.

Richard B Thompson (RB)

Department of Biochemistry and Molecular Biology, University of Maryland School of Medicine, Baltimore, MD 21201, USA.

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Classifications MeSH