Mouse Models of Mineral Bone Disorders Associated with Chronic Kidney Disease

被引:3
|
作者
Zaloszyc, Ariane [1 ,2 ]
Bernardor, Julie [3 ,4 ,5 ]
Bacchetta, Justine [5 ,6 ,7 ,8 ]
Laverny, Gilles [9 ,10 ,11 ,12 ,13 ]
Schmitt, Claus Peter [14 ]
机构
[1] Hop Hautepierre, Hop Univ Strasbourg, Serv Pediat, F-67000 Strasbourg, France
[2] UMR 7515 CNRS Univ Strasbourg, Inst Chim & Proc Energie Environm & St ICPEES, F-67087 Strasbourg, France
[3] Hop Archet, Serv Nephrol Pediat, CHU Nice, F-06202 Nice, France
[4] Univ Cote Azur, Fac Medecine, F-06107 Nice, France
[5] INSERM UMR S1033 Res Unit, F-69008 Lyon, France
[6] Hop Femme Mere Enfant, Reference Ctr Rare Renal Dis, Pediat Nephrol Rheumatol & Dermatol Unit, F-69500 Bron, France
[7] Hop Femme Mere Enfant, Reference Ctr Rare Dis Calcium & Phosphate Metab, Pediat Nephrol Rheumatol & Dermatol Unit, F-69500 Bron, France
[8] Univ Claude Bernard Lyon 1, Lyon Est Med Sch, F-69003 Lyon, France
[9] Inst Genet & Biol Mol & Cellulaire, F-67400 Illkirch Graffenstaden, France
[10] Ctr Natl Rech Sci, UMR7104, F-67400 Illkirch Graffenstaden, France
[11] Inst Natl St & Rech Med, U1258, F-67400 Illkirch Graffenstaden, France
[12] Univ Strasbourg, IGBMC, F-67400 Illkirch Graffenstaden, France
[13] French Network Rare Bone Dis, OSCAR, F-94270 Le Kremlin Bicetre, France
[14] Univ Hosp Heidelberg, Ctr Pediat & Adolescent Med, D-69120 Heidelberg, Germany
关键词
CKD; mice; CKD-MBD; renal osteodystrophy; VASCULAR CALCIFICATION; RENAL OSTEODYSTROPHY; CKD-MBD; PARATHYROID-HORMONE; 5/6; NEPHRECTOMY; KNOCKOUT MICE; ANIMAL-MODEL; TURNOVER; MICROARCHITECTURE; HISTOMORPHOMETRY;
D O I
10.3390/ijms24065325
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Patients with chronic kidney disease (CKD) inevitably develop mineral and bone disorders (CKD-MBD), which negatively impact their survival and quality of life. For a better understanding of underlying pathophysiology and identification of novel therapeutic approaches, mouse models are essential. CKD can be induced by surgical reduction of a functional kidney mass, by nephrotoxic compounds and by genetic engineering specifically interfering with kidney development. These models develop a large range of bone diseases, recapitulating different types of human CKD-MBD and associated sequelae, including vascular calcifications. Bones are usually studied by quantitative histomorphometry, immunohistochemistry and micro-CT, but alternative strategies have emerged, such as longitudinal in vivo osteoblast activity quantification by tracer scintigraphy. The results gained from the CKD-MBD mouse models are consistent with clinical observations and have provided significant knowledge on specific pathomechanisms, bone properties and potential novel therapeutic strategies. This review discusses available mouse models to study bone disease in CKD.
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页数:20
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