Summary

Microdissection of the Rodent Eye

Published: April 21, 2023
doi:

Summary

This paper presents a protocol for ocular micro-dissection in rodents. The process involves the enucleation of the eyeball along with the nictitating membrane (i.e., the third eyelid). This is then followed by the separation of the posterior and anterior eye cups.

Abstract

The ocular micro-dissection of the rodent eye involves the segmentation of the enucleated eyeball with the attached nictitating membrane, or third eyelid, to obtain the anterior and posterior eyecups. With this technique, the sub-parts of the eye, including the corneal tissue, neural tissue, retinal pigment epithelial (RPE) tissue, and lens, can be obtained for wholemounts, cryo-sectioning, and/or single-cell suspensions of a specific ocular tissue. The presence of the third eyelid presents unique and significant advantages, as it benefits the maintenance of the orientation of the eye, which is important for understanding eye physiology following any localized intervention or in studies involving ocular analysis relating to the eye's spatial topography.

In this method, we enucleated the eyeball at the socket along with the third eyelid by carefully and slowly cutting through the extraocular muscles and severing the optic nerve. The eyeball was pierced through the corneal limbus using a microblade. The incision was used as the point of entry, allowing for cutting along the corneal-scleral junction by inserting micro-scissors through the incision point. Small and continuous cuts along the circumference were made until the cups separated. These could be further dissected by gently peeling the translucent layer of the neural retina using Colibri suturing forceps to obtain the neural retina and RPE layers. Further, three/four equidistant cuts were made from the periphery perpendicularly to the optic center until the optic nerve was reached. This opened the hemispherical cups into a floret shape so that they fell flat and could be easily mounted. This technique has been used in our lab for corneal wholemounts and retinal sections. The presence of the third eyelid delineates the nasal-temporal orientation, which allows for the study of various cell therapy interventions post-transplantation and, thus, the targeted physiological validation vital for visualization and accurate representation in such studies.

Introduction

Ocular dissection is an important technique in ophthalmic research and has allowed investigators to access the segments of the eye for targeted studies. Previously, ocular researchers relied on the ocular tissue from diseased individuals for their studies. However, the progressively growing number of strains of ophthalmic rodent models1 over the years has diminished the need for human ocular tissue. These mouse strains have permitted a deeper understanding of ocular disease and interventions. Yet, they have also generated a need for innovative techniques of ocular micro-dissection. The small size and limited area of operation severely constrain effective access to the ocular sub-parts. Further, owing to the homogenous cellular assembly of the posterior and anterior eyecups, it is difficult to conduct targeted interventions post-dissection. The current micro-dissection techniques of laser2 and surgical microdissection3,4 are inadequate in meeting such requirements of ocular research. Laser micro-dissection is very effective in single-cell analysis, but the specific tissue needs to be micro-dissected before the laser procedure2. The technique can isolate small regions of interest from a pre-dissected tissue for molecular analysis. Thus, the technique is not suitable for preparing wholemounts or for the isolation of axially packed ocular layers for optimum visualization.

The surgical method is the most widely used technique; this method involves immobilizing the eye via the optic nerve5 and then performing the dissection. This practice is arduous and can damage any fragile tissue, as the spherical eye continues to move during dissection. Despite being beneficial for isolating the various sections of the retinal layers, the technique cannot demarcate the spatial orientation of the tissue upon dissection.

During dissection, maintaining the presence of the attached nictitating membrane or the third eyelid (Figure 1) presents unique and significant advantages. In this method, first, the eyeball is enucleated with the third eyelid. Then, the third eyelid is used to immobilize the eye6 (Figure 2A). This is followed by piercing the eyeball through the corneal limbus and using the incision as the point of entry (Figure 2B,C). Then, the eyecups are separated by cutting along the circumference anteriorly and posteriorly (Figure 2DG). By dissecting the posterior eyecup further, the translucent layer of the neural retina can be identified and gently peeled off. Three or four equidistant cuts are then made in the obtained hemispherical anterior and posterior cups, which allow these flower-shaped cups to fall flat onto a slide (Figure 2H).

The third eyelid aids in easy and efficient handling during the dissection, thus ensuring minimal damage to the tissue while accessing the various ocular layers and when producing wholemounts. Further, the presence of the third eyelid helps to locate and examine localized interventions during visualization.

The procedure, in our lab, has been performed on a CBA/J or an rd1 mouse strain at P28 of any sex. The procedure can be performed on any strain, age, or sex of animal and has no bias according to these characteristics.

The animals were procured from commercial sources (see Table of Materials) and maintained at the Small Animal Facility (SAF) at the National Institute of Immunology (NII). They were kept in individual ventilated cages (IVC) and received ad libitum access to acidified autoclaved water and food. They were maintained at 21-23 °C and with a 14 h/10 h light/dark cycle.

Given below is a modified surgical method for the micro-dissection of a mouse eye.

Protocol

This procedure was approved by the Institutional Animal Ethics Committee of the National Institute of Immunology, New Delhi. The serial reference number of the approval is IAEC#480/18. The experiments were performed in accordance with the regulation guidelines of the Committee for Control and Supervision of Experiments on Animals, Ministry of Fisheries, Animal Husbandry and Dairying, Government of India, under the supervision of a professional Veterinarian at the SAF, NII. 1. Preparation…

Representative Results

A wholemount of rd1 mouse eye/corneal tissue was prepared to study potential lymph-angiogenesis in the anterior/corneal tissue in a diseased state. The attached conjunctival tissue from the third eyelid acted as a positive control, since the cornea lacks lymphatic vessels. For the study, the corneal tissue was dissected with the conjunctiva and was fixed with 4% PFA, followed by permeabilization and blocking. The tissue was then stained with a primary antibody against the lymphatic endothelial marker (LYVE1)<sup class="x…

Discussion

Ocular microdissection has been found to be a difficult task owing to the small size and spherical shape of the rodent eye, and the rodent eye requires innovative techniques for efficient handling8.

In the current demonstrated method, the enucleated mouse eyeball is obtained with the third eyelid attached for effective and easy handling. Using the third eyelid, the eyeball can be immobilized completely, which allows the dissection to proceed with ease and with minimal …

Offenlegungen

The authors have nothing to disclose.

Acknowledgements

Dr. Alaknanda Mishra, Department of Cell Biology and Human Anatomy, University of California Davis, USA, trained us in this method at the National Institute of Immunology, New Delhi. This work was supported by the core grant received from the Department of Biotechnology, Government of India to the National Institute of Immunology, New Delhi. P.S. was granted a research fellowship by the Department of Biotechnology.

Materials

Acetaminophen (Biocetamol) EG Pharmaceuticals No specific Catalog Number (Local Procurement)
Alkaline Phosphatase Kit (DEA) Coral Clinical System, India No specific Catalog Number (Local Procurement)
Automated analyser Tulip, Alto Santracruz, India Screen Maaster 3000 Biochemical analyser for liver functional test
Betadine (Povidon-Iodine Solution) Win-Medicare;  India No specific Catalog Number (Local Procurement)
Biological safety cabinet ( Class I) Kartos international; India No specific Catalog Number (Local Procurement)
Bright Field Microscope Olympus, Japan LX51
CBA/J inbred mice The Jackson Laboratory Stock No. 000654
Cefotaxime (Taxim) AlKem ; India cefotaxime sodium injection, No specific Catalog Number (Local Procurement)
Cell Strainer Sigma ; US CLS431752
Collagenase Type I Gibco by Life Technologies 17100-017
Cotton Buds Pure Swabs Pvt Ltd ; India No specific Catalog Number (Local Procurement)
DPX Mountant Sigma ; US 6522
Drape Sheet JSD Surgicals, Delhi, India No specific Catalog Number (Local Procurement)
Eosin Y solution, alcoholic Sigma ; US HT110132
Forceps Major Surgicals; India No specific Catalog Number (Local Procurement)
Gas Anesthesia System Ugo Basile; Italy 211000
Glucose Himedia, India GRM077
Hair removing cream (Veet) Reckitt Benckiser , India No specific Catalog Number (Local Procurement)
Hematoxylin Solution, Mayer's Sigma ; US MHS16
Heparin sodium salt Himedia; India RM554
Hyaluronidase From Sheep Testes Sigma ; US H6254
I.V. Cannula (Plusflon) Mediplus, India Ref 1732411420
Insulin Syringes BD ; US REF 303060
Isoflurane ( Forane) Asecia Queenborough No B506 Inhalation Anaesthetic
Ketamine (Ketamax) Troikaa Pharmaceuticals Ltd. Ketamine hydrochloride IP, No specific Catalog Number (Local Procurement)
Meloxicam (Melonex) Intas Pharmaceuticals Ltd; India No specific Catalog Number (Local Procurement)
Micro needle holders straight & curved Mercian ;  England BS-13-8
Micro needle holders straight &
curved
Mercian ;  England BS-13-8
Microtome Histo-Line Laboratories, Italy MRS3500
Nylon Thread Mighty ; India No specific Catalog Number (Local Procurement)
Paraformaldehyde Himedia; India GRM 3660
Percoll GE Healthcare 17-0891-01
Refresh Tears/Eyemist Gel Allergan India Private Limited/Sun Pharma, India P3060 No specific Catalog Number
RPMI Himedia; India No specific Catalog Number (Local Procurement)
Scalpel Major Surgicals; India No specific Catalog Number (Local Procurement)
Scissors Major Surgicals; India No specific Catalog Number (Local Procurement)
SGOT (ASAT) KIT Coral Clinical System, India No specific Catalog Number (Local Procurement)
SGPT (ALAT) KIT Coral Clinical System, India No specific Catalog Number (Local Procurement)
Shandon Cryotome E Cryostat Thermo Electron Corporation ; US No specific Catalog Number
Sucrose Sigma ; US S0389
Surgical Blade No. 22 La Medcare, India No specific Catalog Number (Local Procurement)
Surgical Board Locally made No specific Catalog Number (Local Procurement)
Surgical White Tape 3M India ; India 1530-1 Micropore Surgical Tape
Sutures Ethicon, Johnson & Johnson, India NW 5047
Syringes (1ml, 26 G) Dispo Van; India No specific Catalog Number (Local Procurement)
Trimmer (Clipper) Philips NL9206AD-4 DRACHTEN QT9005
Weighing Machine Braun No specific Catalog Number (Local Procurement)
William's E Media Himedia; India AT125
Xylazine (Xylaxin) Indian Immunologicals Limited Sedative, Pre-Anaesthetic, Analgesic and muscle relaxant

Referenzen

  1. Choi, Y., et al. Studying cancer immunotherapy using patient-derived xenografts (PDXs) in humanized mice. Experimental and Molecular Medicine. 50 (8), 1-9 (2018).
  2. Sutherland, C., et al. Laser Capture Microdissection of Highly Pure Trabecular Meshwork from Mouse Eyes for Gene Expression Analysis. J Vis Exp. (136), e57576 (2018).
  3. Fernandez-Godino, R., Garland, D. L., Pierce, E. A. Isolation, culture and characterization of primary mouse RPE cells. Nature Protocols. 11 (7), 1206-1218 (2016).
  4. Shang, P., Stepicheva, N. A., Hose, S., Zigler, J. S., Sinha, D. Primary cell cultures from the mouse retinal pigment epithelium. Journal of Visualized Experiments. (133), e56997 (2018).
  5. Claybon, A., Bishop, A. J. Dissection of a mouse eye for a whole mount of the retinal pigment epithelium. Journal of Visualized Experiments. (48), e2563 (2011).
  6. Steven, P., et al. Experimental induction and three-dimensional two-photon imaging of conjunctiva-associated lymphoid tissue. Investigative Ophthalmology and Visual Science. 49 (4), 1512-1517 (2008).
  7. Tual-Chalot, S., Allinson, K. R., Fruttiger, M., Arthur, H. M. Whole mount immunofluorescent staining of the neonatal mouse retina to investigate angiogenesis in vivo. Journal of Visualized Experiments. (77), e50546 (2013).
  8. Ullmann, J. F., Moore, B. A., Temple, S. E., Fernandez-Juricic, E., Collin, S. P. The retinal wholemount technique: A window to understanding the brain and behaviour. Brain, Behavior and Evolution. 79 (1), 26-44 (2012).
  9. Nakao, S., Hafezi-Moghadam, A., Ishibashi, T. Lymphatics and lymphangiogenesis in the eye. Journal of Ophthalmology. 2012, 783163 (2012).
  10. Mishra, A., et al. Peripheral blood-derived monocytes show neuronal properties and integration in immune-deficient rd1 mouse model upon phenotypic differentiation and induction with retinal growth factors. Stem Cell Research and Therapy. 11 (1), 412 (2020).

Play Video

Diesen Artikel zitieren
Mohan, K. V., Sinha, P., Swami, B., Muniyasamy, A., Nagarajan, P., Upadhyay, P. Microdissection of the Rodent Eye. J. Vis. Exp. (194), e64414, doi:10.3791/64414 (2023).

View Video