Research Perspective Volume 2, Issue 7 pp 453—456

Figure 1. E4B transgenic (Tg) mice as a new obesity model with hypothalamic neurodegeneration. (A) Immunofluorescence analysis of the PVN region of 6-month-old wild-type (WT) or E4B(ΔU) Tg mice and of a 4-month-old E4B Tg mouse. Brain slices were stained with antibodies to polyubiquitin (green) and to p62 (red), and nuclei were stained with Hoechst 33258 (blue). Protein aggregates reacted with both types of antibody in the PVN region of E4B Tg mice, but not in that of WT or E4B(ΔU) Tg mice. (B) Immunofluorescence analysis of the PVN region of 10-week-old WT or E4B Tg mice with antibodies to glial fibrillary acidic protein (GFAP, red). Nuclei were stained with Hoechst 33258 (blue). SCN and 3V indicate the suprachiasmatic nucleus and third ventricle, respectively. The number of GFAP-positive glial cells in and around the PVN was increased in E4B Tg mice, indicative of gliosis associated with neurodegeneration. (C) Obesity in E4B Tg mice. The gross appearance of an E4B Tg mouse and a WT littermate at 9 months of age is shown on the left. The time course of body weight (BW) for WT mice and E4B Tg lines harboring one or two alleles of the transgene is shown on the right. The extent of obesity in the Tg animals harboring two alleles of the transgene was about twice that in littermates harboring only one allele, indicating that the obese phenotype is directly related to the expression level of the transgene. *P < 0.05, **P < 0.01 for the Tg line with two alleles of the transgene versus wild-type mice.