Summary

Sequentiële Toepassing van dekglaasjes naar de Samenpersende stijfheid van de Muis Lens Assess: Strain en Morfometrische Analyses

Published: May 03, 2016
doi:

Summary

Age-related increases in eye lens stiffness are linked to presbyopia. This protocol describes a simple, cost-effective method for measuring mouse lens stiffness. Mouse lenses, like human lenses, become stiffer with age. This method is precise and can be adapted for lenses from larger animals.

Abstract

De ooglens is een transparante orgaan dat breekt en richt zich licht om een ​​helder beeld op het netvlies te vormen. Bij mensen ciliaire spieren opdracht aan de lens vervormen, wat leidt tot een toename in optische sterkte van de lens te focussen op nabije objecten, een proces dat bekend staat als accommodatie. Leeftijd-gerelateerde veranderingen in lens stijfheid zijn gekoppeld aan presbyopie, een vermindering van de lens vermogen tot accommoderen, en daarmee de noodzaak van een leesbril. Hoewel de muis lenzen niet geschikt of te ontwikkelen presbyopie, kan muismodellen een waardevol hulpmiddel voor genetische begrip lens pathologieën te bieden, en de versnelde veroudering waargenomen in muizen maakt de studie van aan leeftijd gerelateerde veranderingen in de lens. Dit protocol toont op een eenvoudige, nauwkeurige en rendabele werkwijze voor het bepalen muis lens stijfheid, middels dekglaasjes sequentieel toenemende toepassing drukkrachten op de lens. Representatieve gegevens bevestigen dat de muis lenzen worden stijver met de leeftijd, zoalsmenselijke lenzen. Deze werkwijze is sterk reproduceerbaar en kan mogelijk worden opgeschaald naar onderzoekslenzen van mechanisch op grotere dieren.

Introduction

The lens is a transparent and avascular organ in the anterior chamber of the eye that is responsible for fine focusing of light onto the retina. A clear basement membrane, called the lens capsule, surrounds a bulk of elongated fiber cells covered by an anterior monolayer of epithelial cells1,2. Life-long growth of the lens depends on the continuous proliferation and differentiation of epithelial cells at the lens equator into new fiber cells that are added onto previous generations of fiber cells in a concentric manner2. Over time, lens fiber cells undergo compaction, resulting in a rigid center in the middle of the lens called the nucleus1. Accommodation, defined as a dioptric change in the optical power of the eye, occurs in humans when the ciliary muscles contract to deform the lens and allow a true increase in optical power to focus on near objects3-5. In the unaccommodated eye, the lens is held in a relatively flattened state due to tension from zonular fibers. When the ciliary muscles contract, the tension on the lens is released, leading to decreased lens equatorial diameter and increased axial thickness. Age-related changes in the lens cause presbyopia, a progressive loss of lens accommodation, which leads to the need for reading glasses.

Several studies have linked presbyopia to age-related increase in the intrinsic stiffness of the lens6-11. Stiffness is defined as the resistance of an elastic object to deform under applied load. A variety of methods have been used to examine stiffness of human lenses, including spin compression12-14, actuator compression15, probe indentation16, dynamic mechanical analysis 6,10 and bubble-based acoustic radiation force17. While mouse lenses do not accommodate or develop presbyopia, mouse models for lens pathologies are valuable tools because mice are less expensive than larger animals, well characterized genetically and undergo accelerated age-related changes due to rapid aging. A handful of studies have examined mouse lens stiffness with compression methods and demonstrated changes in lens stiffness due to aging or targeted genetic disruptions18-21. Thus, mouse lenses are good models for studying age-related changes in lens stiffness.

This protocol describes a simple and inexpensive, yet precise and reproducible, compression method for determining mouse lens stiffness based on application of glass coverslips onto the lens in conjunction with photographing the lens through a dissection microscope and mirror. This method yields robust strain and morphometric data with an easily fabricated and assembled apparatus. The representative results confirm that mouse lenses increase in stiffness with age.

Protocol

Alle dierlijke procedures werden uitgevoerd in overeenstemming met de aanbevelingen in de gids voor de zorg en het gebruik van proefdieren door de National Institutes of Health en onder een goedgekeurd protocol door de Institutional Animal Care en gebruik Comite op het Scripps Research Institute. 1. Lens Dissection Euthanaseren muizen volgens de aanbevelingen in de National Institutes of Health "Gids voor de Zorg en gebruik van proefdieren" en erkende instelling dier geb…

Representative Results

De stijfheid en de afmetingen van 2-, 4- en 8-maanden oude muizen lenzen werden gemeten. Muizen waren allemaal wild-type dieren op een zuivere C57BL6 stam achtergrond verkregen uit de TSRI Animal Breeding Facility, en elke lens was geladen met 1-10 dekglaasjes. De axiale en equatoriale stammen werden berekend als een functie van de toegepaste belasting door het meten van de axiale en equatoriale diameter van de lens na het toevoegen van elk dekglaasje en vervolgens normaliseren elke wijz…

Discussion

Er zijn een aantal belangrijke overwegingen bij het gebruik van deze methode om de lens stijfheid te meten. Eerst worden de dekglaasjes aangebracht op de lens op een enigszins schuine hoek (8-8,5 °) ten opzichte van de bodem van de kamer (θ). Dit zal een klein bestanddeel van de toepassing equatoriale plaats van axiaal. Echter, dit equatoriale belasting als verwaarloosbaar omdat sin θ ≈ 0,1 19. Wanneer deze methode wordt aangepast voor grotere lenzen, zou de hoek van de dekglaasjes naar de bodem van de k…

Divulgazioni

The authors have nothing to disclose.

Acknowledgements

This work was supported by National Eye Institute Grant R01 EY017724 (VMF) and National Institute of Arthritis and Musculoskeletal and Skin Diseases Grant K99 AR066534 (DSG).

Materials

Fine tip straight forceps Fine Scientific Tools 11252-40
Microdissection scissors, straight edge Fine Scientific Tools 15000-00
Curved forceps Fine Scientific Tools 11272-40
Seizing forceps Hammacher HSC 702-93 Optional
Dissection dish Fisher Scientific 12565154
60mm petri dish Fisher Scientific 0875713A
1X phosphate buffered saline (PBS) Life Technologies 14190
18mm x 18mm glass coverslips Fisher Scientific 12-542A
Measurement chamber with divots to hold lenses Custom-made (see Figure 1)
Right-angle mirror Edmund Optics 45-591
Light source Schott/Fostec 8375
Illuminated dissecting microscope Olympus SZX-ILLD100 With SZ-PT phototube
Digital camera Nikon Coolpix 990

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Citazione di questo articolo
Cheng, C., Gokhin, D. S., Nowak, R. B., Fowler, V. M. Sequential Application of Glass Coverslips to Assess the Compressive Stiffness of the Mouse Lens: Strain and Morphometric Analyses. J. Vis. Exp. (111), e53986, doi:10.3791/53986 (2016).

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