In this application we introduce a novel family of molecules, the PLUNC protein family. PLUNC stands for palate, lung and nasal epithelium clone, as first named in mice. Genomic surveys predict at least nine of these proteins in humans and multiple homologs have been identified in other mammals such as rats, mice and cows. All are small, secreted proteins. Several lines of evidence support the PLUNCs as a discrete mammalian gene family with a role in innate immunity. These include their conserved genomic locus, their similar intron-exon structure, their tissue-specific expression patterns and their predicted protein folds. Specifically, the three-dimensional structure of the PLUNCs is similar to that of an important immune defender, BPI (bactericidal/permeability-increasing protein). BPI dampens the body's response to infection by binding to lipopoylsaccharide (LPS), a component of the outer wall of Gram-negative bacteria. BPI neutralizes LPS and reduces the risk of catastrophic inflammatory responses, including septic shock and death. Given the similarity of PLUNCs to BPI, we propose three specific aims to understand more about this poorly known but diverse mammalian protein family: 1) locate the tissue-specific expression of PLUNC genes in mice, 2) construct mammalian cell lines that secrete multiple isoforms of PLUNC, and 3) test whether these secreted proteins can bind LPS, removing it from the inflammatory cascade. Taken together, the PLUNC proteins represent a novel family of therapeutic targets for the study of innate immunity and the treatment of infection.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Academic Research Enhancement Awards (AREA) (R15)
Project #
2R15HL067220-02
Application #
6953822
Study Section
Special Emphasis Panel (ZRG1-F07 (20))
Program Officer
Berberich, Mary Anne
Project Start
2001-04-20
Project End
2008-12-30
Budget Start
2005-07-15
Budget End
2008-12-30
Support Year
2
Fiscal Year
2005
Total Cost
$107,250
Indirect Cost
Name
De Paul University
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
045694130
City
Chicago
State
IL
Country
United States
Zip Code
60604
Bingle, Lynne; Wilson, Kirsty; Musa, Maslinda et al. (2012) BPIFB1 (LPLUNC1) is upregulated in cystic fibrosis lung disease. Histochem Cell Biol 138:749-58
Musa, Maslinda; Wilson, Kirsty; Sun, Le et al. (2012) Differential localisation of BPIFA1 (SPLUNC1) and BPIFB1 (LPLUNC1) in the nasal and oral cavities of mice. Cell Tissue Res 350:455-64
LeClair, E E; Nomellini, V; Bahena, M et al. (2004) Cloning and expression of a mouse member of the PLUNC protein family exclusively expressed in tongue epithelium. Genomics 83:658-66
Bingle, Colin D; LeClair, Elizabeth E; Havard, Suzanne et al. (2004) Phylogenetic and evolutionary analysis of the PLUNC gene family. Protein Sci 13:422-30
Leclair, E E (2003) Four BPI (bactericidal/permeability-increasing protein)-like genes expressed in the mouse nasal, oral, airway and digestive epithelia. Biochem Soc Trans 31:801-5