Rk. Coker et al., DIVERSE CELLULAR TGF-BETA(1) AND TGF-BETA(3) GENE-EXPRESSION IN NORMAL HUMAN AND MURINE LUNG, The European respiratory journal, 9(12), 1996, pp. 2501-2507
A role for transforming growth factor-beta(1) (TGF-beta(1)) has been p
roposed in lung development and in the pathogenesis of pulmonary disea
se, However, previous studies have not delineated the cells expressing
TGF-beta(1) in normal adult lung, nor compared its gene expression wi
th that of other TGF-beta isoforms. We used digoxigenin-labelled ribop
robes to localize TGF-beta(1) and TGF-beta(3) gene expression in norma
l adult human and mouse lung. This procedure was technically simple, p
roviding excellent resolution. TGF-beta(1) and TGF-beta(3) messenger r
ibonucleic acid (mRNA) transcripts were detected in a wide variety of
cells, In human lung, mRNA for both isoforms was localized to bronchio
lar epithelium and alveolar macrophages. TGF-beta(1), but not TGF-beta
(3) mRNA was detected in mesenchymal and endothelial cells, In murine
tissue, TGF-beta(1), mRNA was localized to bronchiolar epithelium, Cla
ra cells, mesenchymal cells, pulmonary endothelium and alveolar cells,
including macrophages. TGF-beta(3) mRNA was similarly distributed but
not detected in endothelium. In summary, using a nonisotopic techniqu
e in lung tissue, we have detailed the cells expressing the transformi
ng growth factor-beta(1) and beta(3) genes in human and murine lung, T
here was widespread expression of these cytokines in normal lung consi
stent with autocrine or paracrine roles in regulating cellular turnove
r, immune defence and matrix protein metabolism.