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Localization of Misprocessed Pulmonary Surfactant Protein C in Tubular Myelin Enriched Fractions By Cryo Immunogold Labeling

Published online by Cambridge University Press:  02 July 2020

C.-L. Na
Affiliation:
The Children's Hospital Research Foundation, Division of Pulmonary Biology, Cincinnati, OH45229
E. A. Evans
Affiliation:
The Children's Hospital Research Foundation, Division of Pulmonary Biology, Cincinnati, OH45229
H. T. Akinbi
Affiliation:
The Children's Hospital Research Foundation, Division of Pulmonary Biology, Cincinnati, OH45229
T. E. Weaver
Affiliation:
The Children's Hospital Research Foundation, Division of Pulmonary Biology, Cincinnati, OH45229
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Extract

Pulmonary surfactant is secreted by alveolar type II cells and reduces the surface tension at the air-liquid interface of alveoli. After pulmonary surfactant is secreted into the alveolar space, it transforms into tubular myelin, a highly ordered 3-dimensional lattice-like structure. Pulmonary surfactant protein C (SP-C), one of four pulmonary surfactant associated proteins, is synthesized as a proprotein which is processed to biologically active 35 amino acid mature peptide by proteolytic cleavage of N- and C-terminal peptides from the SP-C propeptide (Weaver, 1998). Processing of SP-C is linked to the expression of pulmonary surfactant protein B (SP-B): In SP-B deficient mice, SP-C is misprocessed and present in the bronchoalveolar lavage (BAL; Vorbroker et. al., 1995a). Although the intracellular localization of SP-C is well established (Vorbroker et. al., 1995b), there is no ultrastructure study available regarding the localization of misprocessed SP-C in the airway. In this study, we used transgenic mice expressing a truncated human SP-B propeptide (hSP-BΔC+/+) bred into the murine granulocyte macrophage colony stimulating factor (GMCSF) and SP-B double knockout background (hSP-BΔC+/+: GMCSF-/-: mSP-B-/-) as a model to localize the misprocessed SP-C by cryoimmunogold labeling.

Type
Biological Structure (Cells, Tissues, Organ Systems)
Copyright
Copyright © Microscopy Society of America

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References

References:

1.Akinbi, et. al., J. Biol. Chem. 272 (1997) 9640.CrossRefGoogle Scholar
2.Liou, et al., Histochem. Cell Biol. 106 (1996) 41.CrossRefGoogle Scholar
3.Putman, et. al, Biochem. J. 320 (1996) 599.CrossRefGoogle Scholar
4.Voorhout, et al., Microsc. Res. Tech. 26 (1993) 366.CrossRefGoogle Scholar
5.Vorbroker, et. al., Am. J. Physiol. 268 (1995) L647.Google Scholar
6.Vorbroker, et. al., Am. J. Physiol. 269 (1995) L727.Google Scholar
7.Weaver, , Biochim. Biophys. Acta 1408 (1998) 173.CrossRefGoogle Scholar