Innovations, challenges, and minimal information for standardization of humanized mice.
Renata StripeckeChristian MünzJan Jacob SchuringaKarl-Dimiter BissigBrian SoperTerrence MeehamLi-Chin YaoJames P Di SantoMichael BrehmEstefania RodriguezAnja Kathrin WegeDominique BonnetSilvia GuionaudKristina E HowardScott KitchenFlorian KleinKourosh Saeb-ParsyJohannes SamAmar Deep SharmaFlavia Carla MeottiLivio TrusolinoCarol BultLeonard ShultzPublished in: EMBO molecular medicine (2020)
Mice xenotransplanted with human cells and/or expressing human gene products (also known as "humanized mice") recapitulate the human evolutionary specialization and diversity of genotypic and phenotypic traits. These models can provide a relevant in vivo context for understanding of human-specific physiology and pathologies. Humanized mice have advanced toward mainstream preclinical models and are now at the forefront of biomedical research. Here, we considered innovations and challenges regarding the reconstitution of human immunity and human tissues, modeling of human infections and cancer, and the use of humanized mice for testing drugs or regenerative therapy products. As the number of publications exploring different facets of humanized mouse models has steadily increased in past years, it is becoming evident that standardized reporting is needed in the field. Therefore, an international community-driven resource called "Minimal Information for Standardization of Humanized Mice" (MISHUM) has been created for the purpose of enhancing rigor and reproducibility of studies in the field. Within MISHUM, we propose comprehensive guidelines for reporting critical information generated using humanized mice.
Keyphrases
- endothelial cells
- high fat diet induced
- induced pluripotent stem cells
- pluripotent stem cells
- gene expression
- stem cells
- emergency department
- adipose tissue
- dna methylation
- young adults
- copy number
- skeletal muscle
- transcription factor
- health information
- electronic health record
- smoking cessation
- replacement therapy
- genome wide identification