C. Risco et al., TYPE-II PNEUMOCYTES REVISITED - INTRACELLULAR MEMBRANOUS SYSTEMS, SURFACE CHARACTERISTICS, AND LAMELLAR BODY SECRETION, Laboratory investigation, 70(3), 1994, pp. 407-417
BACKGROUND: Type II pneumocytes, the producers of pulmonary surfactant
, have been extensively studied during the last 20 years because of th
e importance of their metabolism in lung function and integrity. The u
ltrastructural studies of the 1970s and 1980s have shown that these ce
lls present unique elements. EXPERIMENTAL DESIGN: In this work, we use
d thin-section, freeze-fracture, and fracture-flip electron microscopy
techniques to obtain new information on the ultrastructural peculiari
ties of isolated rat type II pneumocytes, focusing our study on the in
tracellular membranous systems and their interrelationships and the mi
croanatomy of their plasma membrane during secretory process. RESULTS:
In thin-sections of pneumocytes postfixed with osmium tetroxide and p
otassium ferricyanide, we observed that lamellar bodies (LBs) are usua
lly connected to membranes of the endoplasmic reticulum, and seem to e
merge and grow from them. Unusual connections between the endoplasmic
reticulum and mitochondria were detected, as well as numerous ''bar-li
ke structures'' (BLSs), most of them in the early stages of developmen
t and often generating from the nuclear membrane. Membranes of the smo
oth endoplasmic reticulum that closely follow the outlines of mitochon
dria also appear to be the origin of some BLSs. Possible transition fo
rms, BLS --> LB, were also detected, although they were rare. New imag
es of the surface of the pneumocytes and its changes during LB secreti
on showed a segregation and clearing of membrane particles at the area
s of LB extrusion. CONCLUSIONS: We propose that LBs can originate dire
ctly from membranes of the endoplasmic reticulum or from BLSs. An indi
rect participation of mitochondria appears possible. The plasma membra
ne of pneumocytes displays structural changes associated with the secr
etion of LBs as visualized by a redistribution of intramembrane and su
rface particles.