Two-step Approach to Explore Early- and Late-stages of Organ Formation in the Avian Model: The Thymus and Parathyroid Glands Organogenesis Paradigm

Summary

This article provides an updated approach to the classical quail-chicken chimera system to study organ formation, by combining novel in vitro and in ovo experimental procedures.

Abstract

The avian embryo, as an experimental model, has been of utmost importance for seminal discoveries in developmental biology. Among several approaches, the formation of quail-chicken chimeras and the use of the chorioallantoic membrane (CAM) to sustain the development of ectopic tissues date back to the last century. Nowadays, the combination of these classical techniques with recent in vitro methodologies offers novel prospects to further explore organ formation.

Here we describe a two-step approach to study early- and late-stages of organogenesis. Briefly, the embryonic region containing the presumptive territory of the organ is isolated from quail embryos and grown in vitro in an organotypic system (up to 48 h). Cultured tissues are subsequently grafted onto the CAM of a chicken embryo. After 10 days of in ovo development, fully formed organs are obtained from grafted tissues. This method also allows the modulation of signaling pathways by the regular administration of pharmacological agents and tissue genetic manipulation throughout in vitro and in ovo developmental steps. Additionally, developing tissues can be collected at any time-window to analyze their gene-expression profile (using quantitative PCR (qPCR), microarrays, etc.) and morphology (assessed with conventional histology and immunochemistry).

The described experimental procedure can be used as a tool to follow organ formation outside the avian embryo, from the early stages of organogenesis to fully formed and functional organs.

Introduction

Avian embryos have been widely used in seminal developmental biology studies. The main advantages of the avian model include the possibility to open the egg, the relatively easy access to the embryo, and the ability to perform micromanipulation. Some examples comprise the classic quail-chicken chimera system for studying cell fate¹, application of specific growth factors to the embryo², and the growth of ectopic cellular structures in the CAM^1,3,4.

To get new insights into distinct stages of organ formation, we have recently developed a method which combines grafting techniques with in vitro manipulation of embryonic tissues⁵. The two-step approach enables the discrimination and exploration of both early- and late-stages of organogenesis, which are often limited due to highly dynamic and complex tissue interactions². Moreover, the lack of suitable tissue-specific markers frequently limits the use of genetically modified animal models⁶. This novel method of the two-step approach largely overcomes such limitations.

To study early-stages of organ formation, in the first step, the quail embryonic territory comprising the prospective organ rudiment is isolated and grown in an in vitro organotypic system for 48 h. During this period, pharmacological modulation of specific signaling pathways can be performed by adding drugs to the culture medium^5,7. Additionally, cultured tissues can be collected at any stage of in vitro growth and probed for gene-expression (using methods such as qPCR, microarrays, etc.).

In the second step, 48 h-cultured tissues are then grafted onto the CAM of a chicken (c) embryo at embryonic day (E) 8 (cE8) (Hamburger and Hamilton (HH)-stages 33-35)⁸. The CAM behaves as a vascular supplier of nutrients and allows gas exchanges^1,3,4 to grafted tissues enabling its development in ovo for longer periods of time. This experimental step is especially well suited to study late-stages of organogenesis, as fully formed organs can be obtained after 10 days of in ovo development^5,9,10,11. Morphological analysis is easily performed by conventional histology to confirm proper organ formation and donor origin of cells can be identified by immunohistochemistry using species-specific antibodies (i.e., MAb Quail PeriNuclear (QCPN)). During the CAM incubation period, grafts can also be grown in the presence of pharmacological agents and collected at any stage of development to evaluate the progression of organogenesis.

The two-step approach, described here in depth, has already been employed in Figueiredo et al.⁵ to explore the avian parathyroid/thymus common primordium development. Accordingly, the inherent particularities of the embryonic territories and stages of development involved in the organogenesis of the thymus and parathyroid glands will be presented below.

The thymus and parathyroid glands epithelia, though functionally distinct, derive from the endoderm of the pharyngeal pouches (PP)¹². In avian, the epithelia of these organs originate from the third and fourth PP endoderm (3/4PP)¹², while in mammals the thymic epithelium derives from the 3PP and the epithelium of parathyroid glands derives from the 3PP and 3/4PP in mouse and human, respectively^13,14.

One of the earliest stages in the formation of these organs is the emergence of discrete thymus and parathyroid domains in the common primordium. In chicken, these domains can be identified by in situ hybridization, with specific molecular markers, at E4.5¹⁵. As development proceeds, these organ rudiments individualize and separate from the pharynx, while a thin mesenchymal capsule, formed by neural crest-derived cells, surrounds them (at E5; HH-stage 27). Later on, the thymic epithelium is colonized by hematopoietic progenitor cells (at E6.5; HH-stage 30)¹².

As in classical quail-chicken studies^1,12, the two-step approach is particularly useful to study the formation of hematopoietic/lymphoid organs, namely the thymus⁵. As the quail explant, with the organ rudiment, is grafted in the chicken embryo prior to hematopoietic progenitor cell colonization, a chimeric thymus is formed with chicken blood-borne progenitor cells infiltrating a quail thymic epithelial counterpart. This method is, therefore, a useful tool to explore the contribution of hematopoietic cells in the development of the avian hemato/lymphoid system.

Protocol

All these experiments follow the animal care and ethical guidelines of the Centro Académico de Medicina de Lisboa.

1. Incubation of Fertilized Quail and Chicken Eggs

1. Incubate Japanese quail (Coturnix coturnix japonica) and chicken (Gallus gallus) fertilized eggs for 3 and 8 days, respectively.
   1. Place the eggs with the air chamber (egg blunt end) facing up in a humidified incubator at 38 °C.
   2. Use around 20 quail eggs and 40 chicken eggs to perform this experiment.
      NOTE: These numbers should be doubled when establishing this procedure for the first time.

2. Isolation of Quail Embryonic Region Containing the Presumptive Territory of Thymic and Parathyroid Rudiments

Note: Perform egg manipulation procedures in sterile conditions using a horizontal laminar flow hood and sterilized instruments and materials.

1. Prepare a large borosilicate glass bowl about 3/4 filled with cold phosphate-buffered saline (PBS) solution.
2. Open a quail egg after 3 days of incubation by tapping the shell and cutting a circular opening on the opposite side of its blunt end with curved scissors. Carefully remove pieces of shell and transfer the embryo to the glass bowl filled with cold PBS.
3. Hold the quail (q) embryo at E3 (qE3) (the quail stage corresponding to the HH-stage 21 of the chicken) with the help of thin forceps. Make a cut into the vitelline membrane enveloping the yolk using curved scissors. Continue to cut around and externally to the circumference of extra-embryonic vessels.
4. Transfer the embryo to a small bowl about 3/4 filled with cold PBS with the help of thin forceps. Thoroughly wash the embryo from the remaining attached yolk.
5. Use a skimmer to transfer the embryo to a 100 mm glass Petri dish with black base (see Table of Materials) containing 10 mL of cold PBS.
6. Place the Petri dish under a stereomicroscope.
   Note: From this point forward, perform the microsurgery procedures under a stereomicroscope for progressive magnification. As an illumination source, it is advised to use LED lights incorporated in the stereomicroscope or in the optic fibers, considering the limited heat load.
7. Hold the embryo to the bottom of the plate with thin insect pins. Place four pins forming a square shape in the extra-embryonic region.
8. Remove the extra-embryonic membranes of the cephalic region with the help of thin forceps and place a fifth pin there.
   Note: If the embryo is correctly positioned, then the otic vesicle, the heart tube, and the 1^st, 2^nd, and 3^rd pharyngeal arches (PAs) should be visible.
9. Dissect the embryonic region of interest, i.e., the 3^rd and 4^th pharyngeal arch region (3/4PAR), using Wecker eye scissors.
   1. Start cutting longitudinally and parallel to the embryo axis, between the somite/neural tube area and the PAs.
   2. Remove the ventrally positioned heart tube by cutting it. Keeping the scissors in the same position, rotate the Petri dish to reposition the embryo according to the direction of the cut.
   3. Cut between the 2^nd and 3^rd PAs and below the 4^th PA.
   4. Detach the remaining membranes from the 3/4PAR with the help of thin forceps.
10. Aspirate the isolated tissues (the 3/4PAR) and transfer them to a glass dish 3/4 filled with cold PBS using a 2 mL sterile plastic pipette.
    Note: Hereafter, tissues can be grown in vitro up to 48 h or be immediately grafted onto the CAM of a chicken embryo at E8.
11. Keep the glass dish containing the isolated 3/4PAR on ice during the preparation of the in vitro assay.

3. In Vitro Organotypic Assay: Culture of the Embryonic Region Containing the Presumptive Territory of Thymic and Parathyroid Rudiments

1. Prepare the culture medium with RPMI-1640 Medium supplemented with 10% FBS and 1% penicillin/streptomycin.
   NOTE: Soluble pharmacological reagents can be added to the medium (for example, LY-411.575 (Ly) and di-benzazepine or cyclopamine and vismodegib, to inhibit Notch and Hedgehog (Hh) signaling pathways, respectively. For this assay, use 50-200 nM of Ly or 5-15 µM of Di-benzazepine to inhibit Notch signaling in the 3/4PAR. Use 20 µM of cyclopamine or 10 µM of vismodegib to inhibit Hh signaling in the 3/4PAR⁵.
2. Prepare the in vitro culture of the 3/4PP explant in a 6-well plate.
   1. Fill one well from the 6-well plate with 5 mL of culture medium. Place a 24 mm Polycarbonate Membrane Insert (see Table of Materials) on the well with the help of thin forceps.
   2. Under the stereomicroscope, transfer the 3/4PAR explant from the glass dish to the membrane surface by gently sliding with the help of a transplantation spoon (or spatula) and thin forceps. Place the explants with the ventral side up and the dorsal side in contact with the membrane. Add up to seven explants per membrane insert. Proceed to step 3.4.
3. Alternatively, culture explants in floating membrane filters.
   1. Prepare a 35 mm Petri dish with 5 mL of culture medium. With the help of thin forceps, float a membrane filter (see Table of Materials) and keep a dry surface in contact with air.
   2. Under the stereomicroscope, transfer the 3/4PAR explant from the glass dish to the membrane filter by gentle sliding with the help of a transplantation spoon (or spatula) and thin forceps. Place the explants with the ventral side up and the dorsal side in contact with the membrane. Add up to 8 explants per membrane filter.
4. Carefully place the explants prepared in steps 3.2 and 3.3 in a humidified incubator at 37 °C with 5% CO₂.
5. After a 48 h incubation period, remove the 6-well plate and the 35 mm Petri dish from the incubator.
   1. Collect the cultured explants from the membrane insert of the 6-well plate.
      1. Add PBS at room temperature (RT) to the membrane insert.
      2. Detach the explants from the membrane by vigorous flushing using a 2 mL sterile plastic pipette.
      3. With the help of the spatula and thin forceps, transfer the cultured explants to a glass dish 3/4 filled with PBS at RT.
   2. Similarly, collect the cultured explants from the floating membrane filter in the 35 mm Petri dish.
      1. Transfer the membrane filter with thin forceps to a new 35 mm Petri dish filled with PBS at RT.
      2. Detach the explants from the membrane filter by vigorous pipetting using a 2 mL sterile plastic pipette.
      3. With the help of thin forceps, discharge the explant-free membrane filter after confirming that no explants remained attached to it.
      4. With a spatula and thin forceps, transfer the explants to a glass dish filled with PBS at RT.
6. Transfer the cultured explants with a spatula to 1 mL of a reagent for total RNA isolation and use for gene-expression studies.
   CAUTION: Exposure to this reagent (see Table of Materials) can be a serious health hazard. Wear appropriate protective eyewear, clothing, and gloves. Follow the handling instructions and read the safety data sheets provided by the manufacturer.
7. Alternatively, graft the cultured tissues onto CAM of chicken embryos at E8. Follow to step 4.

4. Preparation of the CAM

1. Remove the chicken eggs with 8 days of embryonic development from the incubator.
   NOTE: Eggs were incubated with air chamber facing upwards at 38 °C in a humidified incubator.
2. Cover the blunt end of the egg with clear plastic tape to prevent pieces of the shell from falling into the air chamber. Tap the shell and cut a circular opening in the egg with curved scissors. The air chamber should be visible.
3. Remove with caution the white membrane of the air chamber with thin forceps. CAM is then visible and accessible for ectopic tissue transplantation.
   Note: Do not use PBS to hydrate the CAM, before or after transplantation, since PBS promotes sliding and misplacement of the explants. If the membrane dries out, discard the egg.

5. Grafting of Cultured Explants onto the CAM

1. Create small vascular lesions/wounds in the smaller vessels of the CAM with a microscalpel in a holder.
   Note: Use the tip of a Pasteur pipette to remove blood by capillarity in the case of excess bleeding.
2. Use a spatula and thin forceps to transfer the cultured explant to the wounded area of the CAM.
3. Cut a piece of a filter paper slightly larger than the explant and place it on the top of the explant.
   Note: The filter paper helps tracking the explant location after its development in the CAM. Also, it allows daily drug delivery to the explant during in ovo development, if necessary (described in step 5.6).
4. Seal the egg window with clear plastic tape and identify it using a charcoal pencil.
   Note: The plastic tape protects the embryo from dehydration during the incubation period.
5. Incubate the manipulated egg for 10 days in a humidified incubator at 38 °C. Follow to step 6.
6. Optional Step: Daily drug administration during incubation period.
   1. To access the filter, partially lift the plastic tape. Add 100 µL of drug solution, drop by drop, on top of the paper. Re-seal the window and place the egg back in the humidified incubator at 38 °C.
      Note: For this assay, the dose of 20 µM of cyclopamine will inhibit Hh signaling during in ovo development⁵.

6. Ectopic Organ Formation in the CAM After 10 Days of In Ovo Development

1. After 10 days of incubation, remove the egg from the incubator and carefully withdraw the plastic tape.
2. Cut the CAM around the filter region using curved scissors and transfer the CAM-derived explant with filter paper to a small glass bowl about 3/4 filled with cold PBS.
3. With the help of thin forceps transfer the CAM-derived explant to a 100 mm Petri dish with black base containing 10 mL of PBS. Gently remove the filter paper and the excess of membrane using Wecker eye scissors and thin forceps.
4. Transfer the CAM-explant to fixative solution (3.7% PFA in PBS) with a skimmer. Euthanize the chicken embryos without removing them from the egg by making a precise cut in the neck region of the embryo with the help of large scissors.
5. Assess the organ formation in paraffin sections of the CAM-derived explants by conventional histology and immunohistochemistry.

Results

The above described protocol details a method that allows the investigation of both early- and late-stages of organogenesis, often limited by complex cellular and molecular interactions.

This method was previously employed in Figueiredo et al.⁵ to unravel the role of Notch and Hh signaling in the avian parathyroid/thymus common primordium development.

Discussion

A crucial aspect for the success of this method is the quality of both the chicken and quail eggs. Considering the long incubation periods, particularly during the in ovo assay, a good quality of chicken eggs improves viability rates (up to 90%) by the end of the procedure. To achieve this, test eggs from different suppliers. Incubate unmanipulated eggs for long periods (up to 16-17 days) and check their development. To be considered a good quality batch, more than 80% of the embryos should present normal develo...

Materials

List of materials used in this article

Name	Company	Catalog Number	Comments
Chicken fertilized eggs (Gallus gallus)	Pintobar, Portugal		Poultry farm
Quail fertilized eggs (Coturnix coturnix)	Interaves, Portugal		Bird farm
15 mL PP centrifuge tubes	Corning	430052
50 mL PP centrifuge tubes	Corning	430290
60 x 20 mm pyrex dishes	Duran group	21 755 41
100 x 20 mm pyrex dishes	Duran group	21 755 48
Polycarbonate Membrane Insert	Corning	3412	24 mm transwell with 0.4 mm Pore Polycarbonate Membrane Insert
Membrane filter	Millipore	DTTP01300	0.6 mm Isopore membrane filter
6-well culture plates	Nunc, Thermo Fisher Scientific	140675
Petri dish, 35 x 10 mm	Sigma-Aldrich	P5112
Pyrex bowls			from supermarket
Transfer pipettes	Samco Scientific, Thermo Fisher Scientific	2041S	2 mL plastic pipet
Glass pasteur pipette	normax	5426015
Whatman qualitative filter paper	Sigma-Aldrich	WHA1001090	Filter paper
Clear plastic tape			from supermarket
Cytokeratin (pan; acidic and basic, type I and II cytokeratins), clone Lu-5	BMA Biomedicals	T-1302
Cyclopamine hydrate	Sigma-Aldrich	C4116	Pharmacological inhibitor of Hh signalling
Fetal Bovine Serum	Invitrogen, Thermo Fisher Scientific		Standart FBS
Paraformaldehyde	Sigma-Aldrich	P6148
Penicillin-Streptomycin	Invitrogen, Thermo Fisher Scientific	15140-122
Phosphate-Buffered Saline (PBS)	GIBCO, Thermo Fisher Scientific	10010023
QCPN antibody	Developmental Studies Hybridoma Bank	QCPN
RPMI 1640 Medium, GlutaMAX Supplement	GIBCO, Thermo Fisher Scientific	61870010
Bluesil RTV141A/B Silicone Elastomer 1.1Kg Kit	ELKEM/Silmid	RH141001KG	To prepare the back base for petri dish
Stemolecule LY411575	Stemgent	04-0054	Pharmacological inhibitor of Notch signalling
TRIzol Reagent	Invitrogen, Thermo Fisher Scientific	15596026	Reagent for total RNA isolation
Dumont #5 Forceps	Fine Science Tools	11251-30	Thin forceps
Extra fine Bonn scissors, curved	Fine Science Tools	14085-08	Curved scissors
Insect pins	Fine Science Tools	26001-30
Micro spatula	Fine Science Tools	10087-12	Transplantation spoon
Minutien Pins	Fine Science Tools	26002-20	Microscalpel
Moria Nickel Plated Pin Holder	Fine Science Tools	26016-12	Holder
Moria Perforated Spoon	Fine Science Tools	10370-17	Skimmer
Wecker Eye Scissor	Fine Science Tools	15010-11
Camera	Leica Microsystems	MC170 HD
Stereoscope	Leica Microsystems	Leica M80
Microscope	Leica Microsystems	DM2500