Table 1.
Cell line | Animal species | Organ | Cell morphology | ATPase |
---|---|---|---|---|
MDCK | Dog | Kidney | Epithelial | 100 |
CRFK | Cat | Kidney | Epithelial | 45 |
CF2TH | Dog | Thymus | NA | 37 |
PTK2 | Marsupial rat | Kidney | Epithelial | 10 |
LLCPK1 | Pig | Kidney | Epithelial | 6 |
Ma104 | Monkey | Kidney | Epithelial | 0 |
LLCMK2 | Monkey | Kidney | Epithelial | 0 |
NRK E52 | Rat | Kidney | Epithelial | 0 |
VERO | Monkey | Kidney | Epithelial | 0 |
293 | Human fetal | Kidney | Epithelial | 0 |
CHO | Chinese hamster | Ovary | Epithelial | 0 |
COS-7 | Monkey | Kidney | Fibroblast | 0 |
3T3 | Mouse | Embryo | Fibroblast | 0 |
Cells listed in the first column were labeled with CMTMR, mixed in 50:50 proportions with MDCK cells, plated at confluence and incubated overnight. Monolayers were then fixed, treated with a first antibody against the dog β1-subunit, and a second, fluoresceinated one. These were then observed by confocal microscopy as described in Figure 1. One or two hundred borders between MDCK/other cell type were analyzed and scored positive if they exhibited green fluorescence staining. Last column on the right shows the proportion of heterotypic borders exhibiting β1-subunit (except for the first line, where MDCK/MDCK have no heterotypic contacts). This subunit of Na+,K+-ATPase was present in 100% of the homotypic MDCK/MDCK contacts and in a lower proportion in heterotypic ones. NA, not available.