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Humanized mouse models provide a more accurate representation of the human immune microenvironment. This manuscript describes the process in which these models are created through a renal graft of human thymus, injection of human CD34+ cells, and the targeted delivery of human cytokine transgenes to promote CD34+ cell proliferation and differentiation.
Animal models provide a vital translation between in vitro and in vivo biomedical research. Humanized mouse models provide a bridge in the representation of human systems, thereby allowing for a more accurate study of pathogenesis, biomarkers, and many other scientific queries. In this method described, immune-deficient NOD-scid IL2Rγnull (NSG) mice are implanted with autologous thymus, injected with liver-derived CD34+ cells followed by a series of injected cytokine deliveries. In contrast to other models of a similar nature, the model described here promotes an improved reconstitution of immune cells by delivering cytokines and growth factors via transgenes encoded in AAV8 or pMV101 DNA-based vectors. Moreover, it offers long-term stability with reconstituted mice having an average lifespan of 30 weeks after CD34+ injections. Through this model, we hope to provide a stable and impactful method of studying immunotherapy and human disease in a murine model, thus demonstrating the need for predictive preclinical models.
While animal models have created a deeper understanding of cellular and molecular systems, the challenge remains in elucidating the intricacies of species-specific systems, such as immunity, physiology, and other areas of pathology. Non-human primates (NHP), such as chimpanzees, have historically been used to compensate for the wanting gaps in model research; however, the NHP model can be quite costly and inaccessible, particularly as their use has been banned in Europe1.
Following a successful grafting procedure, the murine system replicates the human immune system, as demonstrated through the repopulation of the ly....
All protocols involving the use of animals are closely monitored by the Wistar Institute's Institutional Animal Care and User Committee (IACUC). The laboratory adheres to the guidelines set by this committee and the attending veterinarian to ensure the health, safety, and wellbeing of the animals involved. Prior to following this protocol, veterinarian and IACUC approval are required, and individuals may have variations in the specific surgical techniques and animal handling compared to the protocol per the advice of.......
Following successful surgery and appropriate postoperative injections, CD34+ differentiation can be confirmed via flow cytometry. Approximately 8 weeks after surgery, mice are bled in preparation for FACS, recurring every 2 weeks until a specific threshold of human immune cells is met as is described previously10. Briefly, 100 mL of blood was collected in blood collection tubes coated with lithium and heparin. After the lysis of red blood cells using ACK lysis buffer, the cells were was.......
This manuscript has herein described generating humanized mice via human fetal thymus grafted under the renal capsule and subsequent CD34+ injection to recreate a human immune system.
While the protocol functions to create the best model possible, certain steps are essential to viability. For example, during the CD34+ isolation, it is essential that one looking through the microscope can identify CD34+ cells. Though it may seem redundant, automatic counting mac.......
Thanks to Wistar Flow-Cytometry, Molecular Screening, Vector Core, and Animal Facility for their support. This work was made possible with support from the Dr. Miriam and Sheldon G. Adelson Medical Research Foundation.
....Name | Company | Catalog Number | Comments |
ACK lysis buffer | Life Technologies Corporation | ||
BD Microcontainer | BD | blood collection tubes | |
Busulfan | Sigma | B2635-25g | Irradiating drug; light sensitive |
CD34 Microbeads | Miltenyi Biotec | 130-046-702 | antibody beads kit; stored at 4 °C |
CKIT | Aldevron | custom | cytokine; stored at -20 °C |
Collagenase/Dispase | Roche Diagnostics | 11097113001 | Stored at 4 °C |
FcR Blocking reagent | Miltenyi Biotec | 130-046-702 | antibody beads kit; stored at 4 °C |
Fetal tissue (liver and thymus) | Advanced Bioscience Resources | Delivered same day or overnight | |
Ficoll | GE Healthcare | 17-1440-03 | Stored at room temperature |
FLT3 | Aldevron | 125964 | cytokine; stored at -20 °C |
Forceps | Various | Various | |
Hamilton syringe needle | Various | Various | 22 G; 3 point; 2" length |
Hemostats | Various | Various | |
MS columns | Miltenyi Biotec | 130-042-201 | magnetic separator |
PBS | Gibco | 14190-136 | Stored at room temperature |
Primocin | Invivogen | amt-pm1 | antibiotic; stored at 4 °C |
RPMI | Corning | 10-040-CM | Stored at 4 °C |
SCF | Aldevron | 125962 | cytokine; stored at -20 °C |
Surgical scissors | Various | Various | |
THPO | Aldevron | 125963 | cytokine; stored at -20 °C |
Tissue treated petri dish | Corning | 430167 | |
VetBond glue | 3M | 1469SB | glue |
Visorb suture | Stoelting Co | 5046 | absorbable suture, size 4, 19 mm cutting |
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