Medizinische Universität Graz Austria/Österreich - Forschungsportal - Medical University of Graz

Logo MUG-Forschungsportal

Gewählte Publikation:

Ayabe, T; Satchell, DP; Pesendorfer, P; Tanabe, H; Wilson, CL; Hagen, SJ; Ouellette, AJ.
Activation of Paneth cell alpha-defensins in mouse small intestine.
J Biol Chem. 2002; 277(7):5219-5228 Doi: 10.1074/jbc.M109410200 [OPEN ACCESS]
Web of Science PubMed FullText FullText_MUG

 

Autor*innen der Med Uni Graz:
Altmetrics:

Dimensions Citations:

Plum Analytics:

Scite (citation analytics):

Abstract:
Paneth cells in small intestine crypts secrete microbicidal alpha-defensins, termed cryptdins, as components of enteric innate immunity. The bactericidal activity of cryptdins requires proteolytic activation of precursors by matrix metalloproteinase-7 (MMP-7; matrilysin) (Wilson, C. L., Ouellette, A. J., Satchell, D. P., Ayabe, T., Lopez-Boado, Y. S., Stratman, J. L., Hultgren, S. J., Matrisian, L. M., and Parks, W. C. (1999) Science 286, 113-117). Here, we report on the intracellular processing of cryptdin proforms in mouse Paneth cells. Peptide sequencing of MMP-7 digests of purified natural procryptdins identified conserved cleavage sites in the proregion between Ser(43) and Val(44) as well as at the cryptdin peptide N terminus between Ser(58) and Leu(59). Immunostaining co-localized precursor prosegments and mature cryptdin peptides to Paneth cell granules, providing evidence of their secretion. Extensive MMP-7-dependent procryptdin processing occurs in Paneth cells, as shown by Western blot analyses of intestinal crypt proteins and proteins from granule-enriched subcellular fractions. The addition of soluble prosegments to in vitro antimicrobial peptide assays inhibited the bactericidal activities of cryptdin-3 and -4 in trans, suggesting possible cytoprotective effects by prosegments prior to secretion. Levels of activated cryptdins were normal in small bowel of germ-free mice and in sterile implants of fetal mouse small intestine grown subcutaneously. Thus, the initiation of procryptdin processing by MMP-7 does not require direct bacterial exposure, and the basal MMP-7 content of germ-free Paneth cells is sufficient to process and activate alpha-defensin precursors. MMP-7-dependent procryptdin activation in vivo provides mouse Paneth cells with functional peptides for apical secretion into the small intestine lumen.
Find related publications in this database (using NLM MeSH Indexing)
Amino Acid Sequence -
Animals -
Blotting, Western -
Cloning, Molecular -
DNA, Complementary - metabolism
Dose-Response Relationship, Drug - metabolism
Electrophoresis, Polyacrylamide Gel - metabolism
Immunohistochemistry - metabolism
Intestine, Small - metabolism
Leucine - chemistry
Matrix Metalloproteinase 7 - metabolism
Mice - metabolism
Mice, Inbred BALB C - metabolism
Mice, Inbred C57BL - metabolism
Molecular Sequence Data - metabolism
Paneth Cells - metabolism
Protein Binding - metabolism
Proteins - chemistry
Sequence Homology, Amino Acid - chemistry
Serine - chemistry
Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization - chemistry
Valine - chemistry
alpha-Defensins - metabolism

© Med Uni Graz Impressum