In an effort to develop a suitable bioassay for testing lung growth fa
ctors that might be operative during compensatory lung growth followin
g partial pneumonectomy, a simple and inexpensive lung organ culture s
ystem was characterized. The culture employs lung tissue slices obtain
ed by means of a device allowing thicknesses of 500 mu m to be cut rep
roducibly. To avoid the collapse of the organ, the alveolar spaces wer
e filled prior to culture with Noble agar containing Eagle's-Dulbecco'
s modified medium. Lung tissue sections could be maintained ultrastruc
turally intact for at least one week. The results showed that upon cul
ture, a part of the type II pneumocytes undergo differentiation into t
ype I pneumocytes, thus demonstrating that the culture system may be s
uited for differentiation studies. One surprising feature of this cult
ure system was the mitogenic impulse associated with culture. Radioact
ively labeled thymidine incorporation was strongly stimulated in the c
ulture, mainly affecting the epithelial cells, as could be established
by ''back-to-back'' autoradiography. With a reconstruction experiment
, it was possible to demonstrate the local release of a mitogenic fact
or following slicing, mincing; or dissection of the lung tissue, which
could be assayed by its ability to induce serum-starved Balb/c 3T3 ce
lls to synthesize DNA in culture.