Recently, gut K cells have been shown to express glucokinase,the glucose se
nsor of pancreatic beta cells, and transgenic mice expressing human insulin
under the control of a K cell-specific promoter are resistant to diabetes
development induced by the beta -cell toxin streptozotocin. These novel fin
dings suggest that gut K cells might be a suitable target for gene therapeu
tic treatment of type 1 diabetes mellitus.