Rat alveolar type II cells were isolated following elastase digestion
and cultured on polycarbonate filters at various densities and in diff
erent media. Two days after seeding, the cells formed a monolayer on t
he filters which consisted predominately of type II cells, these then
de-differentiated to a alveolar type I-like cell monolayer by day 6. T
he seeding density and media utilized affected the transepithelial ele
ctrical resistance (TEER) generated by the monolayer. Only certain cul
ture conditions allowed the production of a monolayer that mimics, put
atively, the in vivo alveolar epithelium (TEER greater than 1000 Ohm c
m(2)). V-max and K-m values for the uptake of putrescine by monolayers
exhibiting low and high TEERs on day 6 were determined. The capacity
of the putrescine uptake mechanisms was greater in cell monolayers exh
ibiting a high TEER than those exhibiting a low TEER, suggesting that
the TEER does not only measure the ''tightness'' of the monolayer but
contains an element representative of the viability of the cell monola
yer. The selection of appropriate TEERs for cell culture investigation
s is discussed.