Phenotypic Characterization of the KK/HlJ Inbred Mouse Strain

被引:15
作者
Berndt, A. [1 ]
Sundberg, B. A. [2 ]
Silva, K. A. [2 ]
Kennedy, V. E. [2 ]
Richardson, M. A. [1 ]
Li, Q. [3 ]
Bronson, R. T. [2 ]
Uitto, J. [3 ]
Sundberg, J. P. [2 ]
机构
[1] Univ Pittsburgh, Dept Med, Pittsburgh, PA USA
[2] Jackson Lab, Bar Harbor, ME 04609 USA
[3] Thomas Jefferson Univ, Jefferson Med Coll, Dept Dermatol & Cutaneous Biol, Philadelphia, PA 19107 USA
基金
美国国家卫生研究院;
关键词
systemic mineralization; ectopic mineralization; PXE model; KK/HlJ mice; vibrissae dermal sheath; INDUCED AIRWAY HYPERRESPONSIVENESS; CONNECTIVE-TISSUE MINERALIZATION; GLYCEMIC CONTROL; DATA-CAPTURE; KK MOUSE; MICE; ABCC6; MODEL; RESPONSIVENESS; TOOL;
D O I
10.1177/0300985813501335
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Detailed histopathological diagnoses of inbred mouse strains are important for interpreting research results and defining novel models of human diseases. The aim of this study was to histologically detect lesions affecting the KK/HlJ inbred strain. Mice were examined at 6, 12, and 20 months of age and near natural death (ie, moribund mice). Histopathological lesions were quantified by percentage of affected mice per age group and sex. Predominant lesions were mineralization, hyperplasia, and fibro-osseous lesions. Mineralization was most frequently found in the connective tissue dermal sheath of vibrissae, the heart, and the lung. Mineralization was also found in many other organs but to a lesser degree. Hyperplasia was found most commonly in the pancreatic islets, and fibro-osseous lesions were observed in several bones. The percentage of lesions increased with age until 20 months. This study shows that KK/HlJ mice demonstrate systemic aberrant mineralization, with greatest frequency in aged mice. The detailed information about histopathological lesions in the inbred strain KK/HlJ can help investigators to choose the right model and correctly interpret the experimental results.
引用
收藏
页码:846 / 857
页数:12
相关论文
共 39 条
[1]  
[Anonymous], 1995, Mouse Genetics
[2]  
[Anonymous], 1996, PATHOBIOLOGY AGING M
[3]   The knockout mouse project [J].
Austin, CP ;
Battey, JF ;
Bradley, A ;
Bucan, M ;
Capecchi, M ;
Collins, FS ;
Dove, WF ;
Duyk, G ;
Dymecki, S ;
Eppig, JT ;
Grieder, FB ;
Heintz, N ;
Hicks, G ;
Insel, TR ;
Joyner, A ;
Koller, BH ;
Lloyd, KCK ;
Magnuson, T ;
Moore, MW ;
Nagy, A ;
Pollock, JD ;
Roses, AD ;
Sands, AT ;
Seed, B ;
Skarnes, WC ;
Snoddy, J ;
Soriano, P ;
Stewart, DJ ;
Stewart, F ;
Stillman, B ;
Varmus, H ;
Varticovski, L ;
Verma, IM ;
Vogt, TF ;
von Melchner, H ;
Witkowski, J ;
Woychik, RP ;
Wurst, W ;
Yancopoulos, GD ;
Young, SG ;
Zambrowicz, B .
NATURE GENETICS, 2004, 36 (09) :921-924
[4]  
Bechtold LS, 2000, SYSTEMATIC APPROACH TO EVALUATION OF MOUSE MUTATIONS, P121
[5]   The Mouse Tumor Biology Database (MTB): A Central Electronic Resource for Locating and Integrating Mouse Tumor Pathology Data [J].
Begley, D. A. ;
Krupke, D. M. ;
Neuhauser, S. B. ;
Richardson, J. E. ;
Bult, C. J. ;
Eppig, J. T. ;
Sundberg, J. P. .
VETERINARY PATHOLOGY, 2012, 49 (01) :218-223
[6]   A Single-Nucleotide Polymorphism in the Abcc6 Gene Associates with Connective Tissue Mineralization in Mice Similar to Targeted Models for Pseudoxanthoma Elasticum [J].
Berndt, Annerose ;
Li, Qiaoli ;
Potter, Christopher S. ;
Liang, Yanhua ;
Silva, Kathleen A. ;
Kennedy, Victoria ;
Uitto, Jouni ;
Sundberg, John P. .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2013, 133 (03) :833-836
[7]   Comparison of unrestrained plethysmography and forced oscillation for identifying genetic variability of airway responsiveness in inbred mice [J].
Berndt, Annerose ;
Leme, Adriana S. ;
Williams, Laura K. ;
Von Smith, Randy ;
Savage, Holly S. ;
Stearns, Timothy M. ;
Tsaih, Shirng-Wern ;
Shapiro, Steven D. ;
Peters, Luanne L. ;
Paigen, Beverly ;
Svenson, Karen L. .
PHYSIOLOGICAL GENOMICS, 2011, 43 (01) :1-11
[8]   Quantitative trait loci controlling allergen-induced airway hyperresponsiveness in inbred mice [J].
Ewart, SL ;
Kuperman, D ;
Schadt, E ;
Tankersley, C ;
Grupe, A ;
Shubitowski, DM ;
Peltz, G ;
Wills-Karp, M .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 2000, 23 (04) :537-545
[9]   Airway hyperresponsiveness to acetylcholine: Segregation analysis and evidence for linkage to murine chromosome 6 [J].
Ewart, SL ;
Mitzner, W ;
DiSilvestre, DA ;
Meyers, DA ;
Levitt, RC .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1996, 14 (05) :487-495
[10]  
Frith CH, 1988, COLOR ALAS NEOPLASTI