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Here, we describe a method to transplant and identify human cell spheroids into chick embryos. This xenograft model uses the embryonic microenvironment as a source of instructive signals to assay cell migration, differentiation, and tropism and is especially suited for the study of primary and/or heterogeneous cell populations.
Xenografts are valuable methods to investigate the behavior of human cells in vivo. In particular, the embryonic environment provides cues for cell migration, differentiation, and morphogenesis, with unique instructive signals and germ layer identity that are often absent from adult xenograft models. In addition, embryonic models cannot discriminate self versus non-self tissues, eliminating the risk of rejection of the graft and the need for immune suppression of the host. This paper presents a methodology for transplantation of spheroids of human cells into chicken embryos, which are accessible, amenable to manipulation, and develop at 37 °C.
Spheroids allow the selection of a specific region of the embryo for transplantation. After being grafted, the cells become integrated into the host tissue, allowing the follow-up of their migration, growth, and differentiation. This model is flexible enough to allow the utilization of different adherent populations, including heterogeneous primary cell populations and cancer cells. To circumvent the need for prior cell labeling, a protocol for the identification of donor cells through hybridization of human-specific Alu probes is also described, which is particularly important when investigating heterogeneous cell populations. Furthermore, DNA probes can be easily adapted to identify other donor species. This protocol will describe the general methods for preparing spheroids, grafting into chicken embryos, fixing and processing tissue for paraffin sectioning, and finally identifying the human cells using DNA in situ hybridization. Suggested controls, examples of interpretation of results and various cell behaviors that can be assayed will be discussed in addition to the limitations of this method.
Xenografts are useful tools to investigate the behavior of human cells in vivo. These models have provided invaluable information for a wide range of scientific topics, such as the biology of human stem cells1, the observation of cellular events in real time2, and the investigation of tumoral angiogenesis and metastasis3. In addition, several aspects of cancer biology, including the tumorigenesis of patient-specific xenografts, have been studied4,5. Each of these xenograft models has their advantages and disadvantages and, thus, e....
All in vivo procedures used in this study complied with all relevant experimental guidelines for animal testing and research, in accordance with the Brazilian experimental animal use guidelines (L11794). The protocols used for handling chicken embryos were all approved by the Ethics Committee on the Use of Animals in Scientific Experimentation (Health Sciences Centre of the Federal University of Rio de Janeiro). The use of human cells was approved by the Ethics Committee of the University Hospital Clementino Fra.......
Identification of Alu-positive ADSCs in histological sections
Alu sequences are repetitive elements that comprise ~10% of the human genome and thus are excellent targets for identifying human cells in a species-specific manner43. In situ hybridization with DNA probes can be used to identify genomic elements on histological sections, including primary human cells29,
The protocol described here (Figure 1) presents a feasible option for screening the behavior of primary populations of human cells in vivo, using chick embryos as a model. This paper describes the formation of cell spheroids (Figure 2), transplantation of the spheroid into the chick embryo (Figure 3), processing of specimens and in situ hybridization (Figure 4), representative results .......
This work was supported by Universidade Federal de Rio de Janeiro (UFRJ for J.B.), Conselho Nacional de Desenvolvimento CientÃfico e Tecnológico (CNPq for J.B.) and Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro (FAPERJ for J.B.). We thank T. Jaffredo (CNRS, Paris, France) for the Runx2 (Cbfa1) probe. The HNK1 antibody was obtained from the Developmental Studies Hybridoma Bank developed under the auspices of the NICHD and maintained by The University of Iowa, Department of Biological Sciences, Iowa City, IA 52242 USA. We thank V. Moura-Neto for granting access to the microtome and R. Lent for gr....
Name | Company | Catalog Number | Comments |
Animals | |||
Gallus gallus eggs | Granja Tolomei | SPF-free | White leghorn chicken |
Reagents | |||
Alcian Blue 8GX | Sigma-aldrich | A5268 | |
AluFw primers | Sigma-aldrich | OLIGO | 5’-CGA GGC GGG TGG ATC ATG AGG T-3’ |
AluRev primers | Sigma-aldrich | OLIGO | 5’-TTT TTT GAG ACG GAG TCT CGC-3’ |
Aluminum sulphate | Sigma-aldrich | 368458 | For Nuclear fast red solution preparation |
Anti-Digoxigenin-AP, Fab fragments | Roche | 11093274910 | Antibody Registry ID: AB_514497 |
Anti-Human Natural Killer 1 antibody (HNK1, CD57) | Developmental Studies Hybridoma Bank | 3H5 | Antibody Registry ID: AB_2314644 |
Anti-mouse, goat IgM-HRP | Santa Cruz Biotechnology | sc-2973 | Antibody Registry ID: AB_650513 |
Anti-mouse, goat IgG (H+L)-HRP | Novex | G-21040 | Antibody Registry ID: AB_2536527 |
Anti-Smooth Muscle Actin/ACTA2 antibody | Dako | M085129 | Antibody Registry ID: AB_2811108 |
Aquatex | Merck | 1085620050 | Aqueous mounting agent |
5-Bromo-4-chloro-3-indolyl phosphate p-toluidine salt (BCIP) | Sigma-aldrich | B8503-100MG | |
Blocking Reagent | Roche | 11096176001 | |
Citric acid | VETEC | 238 | For SSC buffer preparation |
Collagenase type IA | Sigma-aldrich | SCR103 | |
dCTP, dGTP, dATP, dTTP set | Roche | 11969064001 | |
Denhardt solution 50X | Invitrogen | 750018 | For hybridization buffer preparation |
Dextran sulphate sodium salt | Thermo Scientific | 15885118 | For hybridization buffer preparation |
DIG RNA Labeling Mix | Roche | 11277073910 | Contains Dig-11-dUTP |
DMEM low-glucose | Sigma-aldrich | D5523 | |
3,3′-Diaminobenzidine tetrahydrochloride (DAB) | Sigma-aldrich | D5905-50TAB | |
N,N-Dimethylformamide (DMF) | Sigma-aldrich | 227056 | For NBT and BCIP solution preparation |
Ethylenediaminetetraacetic acid (EDTA) | Sigma-aldrich | E6758 | For trypsin solution preparation |
Entellan new | Merck | 107961 | Non-aqueous mounting medium |
Ethanol | ProquÃmios | N/A | |
Fetal bovine serum | ThermoFisher | 12657029 | Inactivate at 56 °C before use |
Formaldehyde 37% solution | ProquÃmios | N/A | |
Formamide | Vetec | V900064 | |
Glacial acetic acid | ProquÃmios | N/A | |
India ink | Pelikan | 221143 | |
L-glutamine solution (200 mM) | Gibco | 25030-149 | |
Magnesium chloride | Merck | 8147330100 | For NTM buffer preparation |
Maleic acid | Sigma-aldrich | M0375-500G | For MAB buffer preparation |
Methanol | ProquÃmios | ||
Normal Goat Serum | Sigma-aldrich | NS02L | Inactivate at 56 °C before use |
4-Nitro blue tetrazolium chloride (NBT) | Roche | 11585029001 | |
Nuclear fast red | Sigma-aldrich | 60700 | |
Paraplast Plus | Sigma-aldrich | P3558 | |
Penicillin G sodium salt | Sigma-aldrich | P3032 | |
Phosphate buffered saline (PBS) | Sigma-aldrich | P3813 | |
Phosphomolybdic acid | Merck | 100532 | |
Proteinase K | Gibco BRL | 25530-015 | |
Salmon sperm DNA | Invitrogen | 15632011 | For hybridization buffer preparation |
Sodium chloride | Sigma-aldrich | S9888 | For SSC, MAB and NTM buffer preparation |
Streptomycin Sulfate | Sigma-aldrich | S6501 | |
Taq Polymerase kit | Cenbiot Enzimas | N/A | |
Tris-HCl | Sigma-aldrich | T5941 | |
Trypsin | Sigma-aldrich | T4799 | |
Tween 20 | Sigma-aldrich | P1379 | |
Xylene | ProquÃmios | N/A | |
Microscope and equipments | |||
Axioplan upright microscope | Carl Zeiss Microscopy | N/A | |
Axiovision software | Carl Zeiss Microscopy | N/A | |
Cell incubator | ThermoForma | 3110 | |
Egg incubator- 50 eggs | GP | ||
Gooseneck lamp | Biocam | N/A | For egg manipulation |
Fiji software; Cell Counter plugin | ImageJ | https://imagej.net/software/fiji/ | |
Laminar flow hood | TROX | 1385 | |
Nanodrop Lite | Thermo Scientific | ND-LITE-PR | |
Rotary microtome | Leica Biosystems | RM2125 RTS | For sectioning |
Stereomicroscope | Labomed | Luxeo 4D | For egg manipulation |
Sterilization oven | REALIS | 7261690 | For sterelization of surgical materials |
Consumables | |||
0.2 mL (PCR) polypropylene centrifuge tubes | Eppendorf | 30124707 | |
15 mL polypropylene conical centrifuge tubes | Corning | CLS430791 | |
1.5 mL polypropylene centrifuge tubes | Axygen | MCT-150-C | |
2 mL polypropylene centrifuge tubes | Axygen | MCT-200-C | |
50 mL polypropylene conical centrifuge tubes | Corning | CLS430829 | |
Barrier (Filter) Tips, 200 μL size | Invitrogen | AM12655 | For egg manipulation |
Excavated Glass Block (Staining Block) with Cover Glass | Hecht Karl | 42020010 | |
Embedding cassettes | Simport | M480 | Used as a paraffin block holder |
Glass coverslides, 24 x 40 mm | Kasvi | K5-2440 | |
Glass Pasteur pipettes 230 mm | NORMAX | 5426023 | For preparation of glass capillaries |
Microtome blades | Leica Biosystems | HIGH-PROFILE-DISPOSABLE-BLADES-818 | For sectioning |
Parafilm M | Parafilm | P7793 | |
Plastic Petri dish, 30 mm | Kasvi | K13-0035 | For egg manipulation |
Plastic Petri dish, 60 mm | Prolab | 0303-8 | For cell spheroids preparation. Should not be treated for cell adhesion. |
Silanized glass slides (Starfrost) | Knittel Glass | 198 | For sectioning |
Syringe 1 mL , Needles 26 G (0.45 x 13 mm) | Descarpack | 32972 | For egg manipulation (albumen aspiration) |
Surgical tools | |||
Aspirator tube | Drummond | 2-000-000 | For egg manipulation |
Dissection scissors | Fine Science Tools | 14061-11 | For egg manipulation |
Microforceps (tweezers) | Fine Science Tools | 00108-11 | For egg manipulation and preparation of glass capillaries |
Needle holder (adjustable dissection needle chuck) | Fisherbrand | 8955 | For egg manipulation |
Oil whetstone, 10.000 grit | N/A | N/A | For sharpening needles |
Pair of small paint brushes | N/A | N/A | For handling paraffin sections. Any brand may be used. |
Sewing needles | N/A | N/A | For sharpening into microscalpels. Any brand may be used. |
Sterile disposable scalpel No. 23 | Swann-Norton | 110 | For sectioning |
Surgical scalpel handle | Swann-Norton | 914 | For sectioning |
Wecker iris scissors, sharp/sharp | Surtex | SS-641-11 | For egg manipulation |
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