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Publication : PSP expression in murine lacrimal glands and function as a bacteria binding protein in exocrine secretions.

First Author  Robinson CP Year  1997
Journal  Am J Physiol Volume  272
Issue  4 Pt 1 Pages  G863-71
PubMed ID  9142919 Mgi Jnum  J:40020
Mgi Id  MGI:87359 Doi  10.1152/ajpgi.1997.272.4.G863
Citation  Robinson CP, et al. (1997) PSP expression in murine lacrimal glands and function as a bacteria binding protein in exocrine secretions. Am J Physiol 272(4 Pt 1):G863-71
abstractText  Nonobeese diabetic (NOD) mice, an animal model for type I autoimmune diabetes and autoimmune sialoadenitis, abnormally express parotid secretory protein (PSP) in the submandibular glands (Robinson, C. P, Il. Yamamoto, A. B. Peck, and IM. G. Humphreys-Beher. Clin. Immunol. Immunopathol. 79: 50-59, 1996). To evaluate possible PSP gene dysregulation in the NOD mouse, we have examined a number of organs and tissues for PSP mRNA transcripts and protein expression. Results indicate that PSP is produced in the lacrimal glands of NOD mice as well as most laboratory mouse strains. Although purified salivary PSP from C3H/HeJ or BALB/c mice fails to affect amylase enzyme activity in in vitro assays, PSP bound to whole bacteria in a Zn2+-dependent manner. Additionally, radiolabeled protein bound to specific bacterial membrane proteins using a ligand binding assay. PSP gene transcription, but not protein production, was observed in the heart and pancreas from NOD mice, indicating abnormal transcription of the PSP gene. Sequence analysis of PSP cDNA from NOD mice revealed numerous base differences (compared with the published PSP sequence) capable of leading to significant amino acid substitutions, suggestive of strain-specific differences for the protein in mice. Together these results suggest that there exists in the NOD mouse a dysregulation of PSP transcription in various tissues. However, except for C3H/HeJ mice, PSP appears as a normal product of the lacrimal glands where, as in saliva, it may function as a nonimmune antimicrobial agent in the protection of tissue surfaces exposed to the external environment.
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