Literature DB >> 3355002

Localization of surfactant protein synthesis in human lung by in situ hybridization.

D S Phelps1, J Floros.   

Abstract

In order to investigate the sites of synthesis of the pulmonary surfactant-associated proteins, we performed tissue in situ hybridization. We used frozen sections of human lung tissue and 35S-UTP-labeled cRNA probes to localize mRNAs for the 35 kDa surfactant-associated protein (PSP-A) and for the precursor of one of the hydrophobic, low molecular weight surfactant-associated proteins (PSP-B). We found that PSP-A mRNA is present only in the alveolar epithelial type II cells with alveolar macrophages, bronchiolar epithelium, and other cells of the interstitutium being negative. PSP-B mRNA is present in both alveolar type II cells and in some cells of the bronchiolar epithelium. Macrophages and other cells were negative. The data in this report demonstrate that: (1) type II pneumonocytes are capable of synthesizing both PSP-A and PSP-B, (2) some cells of the human bronchiolar epithelium contain PSP-B mRNA but not PSP-A, and (3) human alveolar macrophages do not synthesize either PSP-A or PSP-B.

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Year:  1988        PMID: 3355002     DOI: 10.1164/ajrccm/137.4.939

Source DB:  PubMed          Journal:  Am Rev Respir Dis        ISSN: 0003-0805


  35 in total

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Review 3.  Function and regulation of expression of pulmonary surfactant-associated proteins.

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Review 5.  Surfactant replacement therapy.

Authors:  M J Kresch; W H Lin; R S Thrall
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6.  Regulation of messenger RNAs for the hydrophobic surfactant proteins in human lung.

Authors:  H G Liley; R T White; R G Warr; B J Benson; S Hawgood; P L Ballard
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7.  Immunogold localization of SP-A in lungs of infants dying from respiratory distress syndrome.

Authors:  D E deMello; S Heyman; D S Phelps; J Floros
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8.  Cap-independent translation of human SP-A 5'-UTR variants: a double-loop structure and cis-element contribution.

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9.  Purification, characterization and cDNA cloning of human lung surfactant protein D.

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10.  Successful establishment of primary small airway cell cultures in human lung transplantation.

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