Avian air capillaries are delicate structures compared to the mammalia
n pulmonary alveolus. A transmission and scanning electron microscopic
study was carried out on several species of birds with the aim of det
ermining the support structures of the avian gas-exchange mantle. Lung
tissue of two bird species belonging to strong flying birds (pigeon a
nd barn owl) and two relatively flightless species (domestic fowl and
quail) was subjected to standard processing for transmission and scann
ing electron microscopy after intratracheal inflation, Twisted profile
s of lipoproteinaceous trilaminar substance as specific secretory prod
uct of avian squamous respiratory cells can be seen in the cell body a
nd cytoplasmic extensions that are wedged between the blood capillarie
s, partly surrounding them, The intracytoplasmatically located trilami
nar complexes from a three-dimensional intricate spiderweb-like system
between the blood capillaries and air capillaries, which presumably f
unction as an anchoring and support structure of the gas-exchange tiss
ue. This system is strengthened by retinacula -pairs of attenuated par
allel processes of squamous respiratory cells that project to the airw
ay lumen -expanding and bridging the opposite side of air capillaries,
The trilaminar substance is discharged in the form of a 15-nm-thick a
cellular lining layer which is uniquely adapted to the extremely thin
respiratory epithelium. The trilaminar substance arises in the cytopla
sm of squamous respiratory cells from profiles of granular and smooth
endoplasmic reticulum. The integrity and stability of the gas-exchange
tissue is likely to be guaranteed by a specific arrangement of the sq
uamous respiratory cells, in which the trilaminar substance plays a pa
ramount role, This general pattern can be observed in strong flying bi
rd species as in the relatively flightless birds.