Cultures of respiratory epithelial cells were obtained from nasal poly
ps collected in patients with and without primary ciliary defect. The
ciliary beating frequency and the ciliary beating heterogeneity were d
etermined on native and cultured tissues. We observed a significantly
higher (p < 0.01) ciliary beating frequency of cultured ciliated cells
, when compared with ciliated cells from the native tissue. The ciliar
y beating frequency of the cultured ciliated cells from the patient wi
th primary defect (7.9 +/- 2.1 Hz) was significantly lower when compar
ed with the beating frequency of the ciliated cells from the control s
ubject (12.4 +/- 2.0 Hz). In addition, the percentage of ciliated cell
s characterized by a beating frequency lower than 8 Hz was 90.7% in th
e native tissue and 47.5% in the cultured tissue from the patient with
ciliary primary defect. In the patient without ciliary primary defect
, 90% of the cultured ciliated cells had a homogeneous ciliary beating
, whereas in the patient with primary ciliary defect, only 47% of the
ciliated cells had a homogeneous ciliary beating. These results sugges
t that the culture of respiratory cells associated with the functional
activity measurement of the ciliated cells represent another way of p
recisely determining the extent of the primary ciliary dyskinesia defe
ct.