Degree Type
Honors Capstone Project
Date of Submission
Spring 5-1-2014
Capstone Advisor
Dr. Guirong Wang
Honors Reader
Dr. John Belote
Capstone Major
Biology
Capstone College
Arts and Science
Audio/Visual Component
no
Capstone Prize Winner
no
Won Capstone Funding
no
Honors Categories
Sciences and Engineering
Subject Categories
Biology
Abstract
Surfactant protein B (SP-B, gene name: sftpb) is essential for normal lung function. It reduces alveoli surface tension, thereby preventing the lung from collapse. A single nucleotide polymorphism (SP-B 1580 C/T) is associated with several lung diseases and altered N-linked glycosylation site at Asn129 of SP-B. This change, present in the human population, has been associated with negative effects on SP-B precursor (proSP-B) processing and function. In this study, hSP-B humanized transgenic mice were generated without mouse SP-B background. Four founding lines, showing only the hSP-B gene, were selected via PCR-based DNA analysis. Genomic sequencing of these mice revealed which allele variant (hSP-B-C/T) they carried. Western blot analysis of BALF samples revealed these hTG mice expressed hSP-B protein in levels significant for survival and comparable to that of a healthy human lung. Characterization of the two hSP-B allele variant hTG strains revealed significant differences in their relative alveolar size and total lipid concentration.
Recommended Citation
Schoenborn, Mark C., "Human Surfactant Protein B Expression in Humanized Transgenic Mice" (2014). Renée Crown University Honors Thesis Projects - All. 767.
https://surface.syr.edu/honors_capstone/767
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