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Here, we describe a protocol for separating yolk, granulosa cells, and theca cells in avian preovulatory follicles. This precision handling enables critical investigations into the role of these layers in reproductive function, aiding the understanding of follicular development, hormonal regulation, and disease research for enhanced agricultural yield and biomedical insights.
Layer hens (egg-laying chickens) and broiler breeders (breeding stock for meat-producing chickens) are crucial to the world's food supply as a reliable source of protein. They are also an emerging animal model for the study of human reproductive disease. As the field of poultry research develops, the health and function of the layer hen and broiler breeder ovary will be an important point of study for both agricultural and biomedical researchers. One of the challenges presented by this emerging interest is the need for replicable techniques that all researchers can employ in ovarian specimen collection. In particular, a detailed visual process must be established to define the proper separation of the specialized granulosa and theca cell layers from hen follicles to achieve agreement and consistency among researchers.
This study describes the extraction of preovulatory follicles and ovary tissue in white leghorn hens of prime reproductive age. The separation of these follicles is performed under cold, liquid conditions to congeal the yolk for easier manipulation and to prevent the follicle's own weight from tearing apart cell layers during the separation process. Once the separation is complete, the desired cell layers can be further digested for tissue culture approaches or can be cryopreserved for genomic and proteomic analyses.
Egg-producing chickens are a key component of the world food supply chain and are an evolving animal model for the study of fertility and ovarian cancer. The chicken has a long history of laboratory use, from in ovo studies of influenza vaccines1 to the study of cancerous tumor growth2, and is a key animal for insight into gonadal development3,4,5. Understanding the role of a hen's reproductive system, in particular, the cyclical nature of ovarian follicular development and the types of cells involved, is an area of....
All animals used in this study were maintained and euthanized per the protocol approved by the University of Delaware's Institutional Animal Care and Use Committee (IACUC Protocol 110R).
1. Preparation
This protocol yields the separation of granulosa and thecal cell layers from the ovarian follicle (Figure 5 and Figure 6). These layers can then be prepared for histological examination to confirm successful separation. These histological images, reviewed and captured by a board-certified veterinary pathologist (EMB), clearly demonstrate the effective separation of the granulosa and theca layers for both the F1 and F5 preovulatory follicles (
This study outlines the procedure for the distinct separation of both granulosa and thecal cell layers from preovulatory follicles in poultry. Unlike the existing method established by Gilbert et al. in 1977, the adaptations made in this method allow for a more controlled environment when manually separating the granulosa cell layer from the theca layer from all preovulatory follicles15. Furthermore, it enables researchers to visualize the granulosa cell layer throughout the whole procedure, enhan.......
We are grateful to Milos Markis (AviServe) for assistance with animal husbandry, Nicole Guarino (University of Delaware) for assistance with manuscript preparation, Evelyn Weaver and Ramesh Ramachandran (The Pennsylvania State University) for assistance with procedure demonstration and manuscript preparation. Figure 2A and Figure 3 were created using BioRender.com using an institutional license sponsored by the University of Delaware Research Office. This work was supported by the UD CANR Comparative Pathology Laboratory. KME is supported by USDA NIFA grant 2023-67011-40333. This work was supported by grants from the University of Del....
Name | Company | Catalog Number | Comments |
3.5 in. Small Glass Bowls, 5 oz | Amazon | B0BXP5PJTN | Autoclavable glass bowls of at least 3.5 in. diameter |
Aluminum Foil | Costco | 720 | Cover autoclave bowls |
Amazon Pet Training Pads, Regular, 100-Count | Amazon | B0B58WTPFS | For use as necrospy pads, any absorbant pad will work |
Autoclave Tape | Fisherbrand | 15-901-111 | |
Cole-Parmer LED Fiber Optic Illuminators | Cole-Parmer | EW-41723-02 | |
Curved Very Fine Precision Tip Forceps | Fisherbrand | 16-100-123 | Non-Serrated |
Dissecting Microscope | Leica | S6E | |
Fine Precision Scissors | Fisherbrand | 12-000-155 | Non-Serrated |
Food Container Boxes with Lid Set of 17 Clear/Green Microwave Freezer Dishwasher Safe | Amazon | B09QGZCRDB | Use any container that can hold ice AND an 3.5 in. small glass bowl |
High Precision 45 Degree Curved Tapered Very Fine Point Tweezers/Forceps | Fisherbrand | 12-000-125 | Non-Serrated |
High Precision Straight Very Fine Point Tweezers/Forceps | Fisherbrand | 16-100-120 | Non-Serrated |
Isopropanol | Fisherbrand | A426P-4 | |
McKesson Specimen Container, Sterile, Screw Cap, Leak-Resistant, 120 mL | McKesson | 16-9526 | 4 oz. / 120 cc, graduated |
Phosphate-buffered saline (PBS, 10x), pH 7.6 | ThermoFisher | J62692.K7 | Will need to be made into 1x PBS |
Spray Bottle | Cole-Parmer | EW-06091-01 | For 70% Isopropanol |
Sterile Surgical Blades #22 | Cincinnati Surgical | 122 | |
Sterilization Pouches 10" x 16" | Amazon | B07MFB455C | |
Tapered Ultrafine Tip Forceps Fisherbrand | Fisherbrand | 16-100-121 | Non-Serrated |
Foam Biopsy Pads, Rectangular | Fisherbrand | 22-038-221 | |
Formalin Solution, 10% (Histological) | Fisher Chemical | SF98-4 | |
Tissue processing/embedding cassettes with lid | Simport M490-2 | Z672122 |
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