M. Bens et al., TRANSIMMORTALIZED MOUSE INTESTINAL-CELLS (M-ICCL2) THAT MAINTAIN A CRYPT PHENOTYPE, American journal of physiology. Cell physiology, 39(6), 1996, pp. 1666-1674
This study describes the properties of a clone of immortalized cells (
m-ICcl2 cells) derived from the bases of small intestinal villi from 2
0-day-old fetuses of L-type pyruvate kinase (L-PK)/TAg1 transgenic mic
e. The mice harbor the simian virus 40 large T antigen under the contr
ol of the 5' regulatory sequence from the L-PK gene. m-ICcl2 cells exp
ressed nuclear large T antigen, had a prolonged life span, and were no
ntumorigenic when injected into nude mice. They formed confluent monol
ayers of cuboid cells separated by tight junctions, developed dense, s
hort apical microvilli, and formed domes. They also possessed cytokera
tins, villin, aminopeptidase N, dipeptidyl-peptidase IV, and glucoamyl
ase and retained crypt cell features, including intracellular sucrase
isomaltase and alpha-L-fucose glycoconjugates accumulation and express
ion of the polymeric immunoglobulin receptor and the cystic fibrosis t
ransmembrane conductance regulator gene. Thus the m-ICcl2 cell line ob
tained by targeted oncogenesis in transgenic mice maintained in cultur
e several important properties and differentiated functions of intesti
nal crypt cells.