This technology is a conditional-knockout mouse line that deletes the retinol-binding protein 2 (Rbp2) gene in intestinal enteroendocrine cells, allowing for the study of retinoid-dependent regulation of gut hormone secretion and its downstream metabolic phenotypes.
Several platforms investigate intestinal-endocrine hormone function, yet none reliably replicate human physiology or inform personalized therapies. Cell‑type-specific models are required to define how Rbp2 in enteroendocrine cells influences hormone release and metabolic outcomes, which global knockouts cannot isolate.
This technology describes a knockout mouse line that deletes retinol-binding protein 2 (Rbp2) specifically in gut endocrine cells. This model was created by introducing loxP sites flanking Rbp2 exon 1 and generating targeted embryonic stem cells that yield a floxed Rbp2 allele. The design permits cell-specific, Cre-driven excision of Rbp2 exon 1. This line is being used in ongoing in vivo studies to assess enteroendocrine-specific effects on hormone secretion and systemic metabolic readouts.
Rossana M. Calderon, M.D.
IR CU25453
Licensing Contact: Joan Martinez