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Association between congenital defects in papillary outgrowth and functional obstruction in Crim1 mutant mice
Author(s) -
Wilkinson Lorine,
Kurniawan Nyoman D,
Phua Yu Leng,
Nguyen Michael J,
Li Joan,
Galloway Graham J,
Hashitani Hikaru,
Lang Richard J,
Little Melissa H
Publication year - 2012
Publication title -
the journal of pathology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.964
H-Index - 184
eISSN - 1096-9896
pISSN - 0022-3417
DOI - 10.1002/path.4036
Subject(s) - major duodenal papilla , renal papilla , kidney , endocrinology , fibrosis , biology , pathology , medicine
Crim1 hypomorphic ( Crim1 $^{KST264/KST264}$ ) mice display progressive renal disease characterized by glomerular defects, leaky peritubular vasculature, and progressive interstitial fibrosis. Here we show that 27% of these mice also present with hydronephrosis, suggesting obstructive nephropathy. Dynamic magnetic resonance imaging using Magnevist showed fast development of hypo‐intense signal in the kidneys of Crim1 $^{KST264/KST264}$ mice, suggesting pooling of filtrate within the renal parenchyma. Rhodamine dextran (10 kDa) clearance was also delayed in Crim1 $^{KST264/KST264}$ mice. Pyeloureteric peristalsis, while present, was less co‐ordinated in Crim1 $^{KST264/KST264}$ mice. However, isolated renal pelvis preparations suggest normal pelvic smooth muscle contractile responses. An analysis of maturation during the immediate postnatal period [postnatal day (P) 0‐15] revealed defects in papillary extension in Crim1 $^{KST264/KST264}$ mice. While Crim1 expression is weak in pelvic smooth muscle, strong expression is seen in the interstitium and loops of Henle of the extending papilla, commencing at the tip of the P1 papilla and disseminating throughout the papilla by P15. These results, as well as implicating Crim1 in papillary extension and pelvic smooth muscle contractility, highlight the previously unrecognized association between defects in papillary development and progression to chronic kidney disease later in life. Copyright © 2012 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.