We used an antisense oligonucleotide (ODN) to inhibit laminin (LM) β1 chain synthesis in mouse embryonic lung explants and cell cultures. The ODN spanned 17 bases located 13 bases downstream the initiation codon and contained phosphorothioate and C-5 propynyl pyrimidine modifications. Penetration of the ODN into the lung explants was confirmed by fluorescein isothiocyanate (FITC) tagging. 50 μM of antisense ODN decreased LM β1 chain synthesis by 82±6.9% with no significant changes in the synthesis of other LM chains. The same antisense probe but without C-5 propynyl pyrimidine modification, another 17-mer ODN complementary to the LM β1 initiation codon, and a 17-mer ODN complementary to the LM α1 initiation codon had no antisense activity. Lung explants exposed to the active LM β1 antisense ODN showed decreased LM-1 and collagen type IV deposition at the epithelial–mesenchymal interface and an arrest in bronchial smooth muscle (SM) development. Histological examination and cell motility assays suggested that this arrest was due to impaired spreading and migration of SM cell precursors over the defective basement membrane (BM). Our studies indicate that β1-chain containing LMs play a role in bronchial myogenesis.