实验动物

不同品系小鼠介绍

SWR小鼠介绍
Introduction of SWR mouse

SWR小鼠(SWR mouse)广泛作为一般实验动物使用,但在肾脏、肺、神经系统、肿瘤、感染、免疫等方面有特殊的研究用途。

毛色:白色。

SWR小鼠的诞生

129小鼠是由Lynch(Clara J Lynch)在1926年前后用Swiss小鼠进行近交筛选培育而成的小鼠。

SWR小鼠的特点与应用

(1) 用于建立转基因小鼠

SWR小鼠具有独特的优势:对外源性激素敏感,核仁大,因而比较适合转基因鼠的母本。

(2) 用于自身免疫性糖尿病的对照

自身免疫性糖尿病小鼠(NOD/ShiLtJ 小鼠)也是来自Swiss小鼠,因此,在该小鼠中研究免疫功能异常的时常采用SWR小鼠作为对照(免疫功能正常)。

(3) 糖尿病相关的肾功能不足

随着年龄增加,发生多饮、多尿等尿崩症表现,主要由于肾小管对抗利尿激素(ADH)的反应能力相对不足,又称为肾源性糖尿病性尿崩症(nephrogenic diabetic insipidus)。

(4) 对实验性脑脊髓炎高度敏感。

SWR小鼠对多发性硬化和实验性脑脊髓炎(experimental allergic encephalomyelitis,EAE)比较敏感,可用于EAE模型建立,详见“Mouse Models of Multiple Sclerosis”。

(5) 对实验性动脉粥样硬化中度敏感

采用高脂高胆固醇模型饲料可以诱导动脉粥样硬化,呈现中度敏感性。

(6)对结核杆菌敏感

感染结核杆菌后,进展速度快,存活时间短,肺中淋巴细胞较多,淋巴细胞分化不明显,CD4+的IFN-γ阳性淋巴细胞少。因此,适合用于进行性致死性肺结核的模型动物。

(7)自发性肿瘤

在4~6周龄时发生自发性卵巢颗粒细胞瘤(Granulosa cell tumors,GCT),因此,用于人类婴儿、儿童和年轻女性的卵巢颗粒细胞瘤模型动物。

老年时肺肿瘤和乳腺肿瘤发生率较高。

(8)用于复苏的动物模型

与其他品系小鼠比较,SWJ小鼠在低氧情况下不容易发生自主复苏反应(autoresuscitation),因而可以作为研究复苏方法的动物模型。由于在12-22日龄期间不能发生自主复苏反应,因而被认为特别适用于SIDS(Sudden Infant Death Syndrome)模型。

(9)对胶原诱导不敏感

胶原虽然能够诱导抗体生成,但是,不能诱导形成关节炎。

SWR小鼠还是唯一的携带Soaa基因的近交小鼠,能够对低浓度蔗糖八乙酸酯(sucrose octaacetate)溶液发生回避反应。

在选择购买饲料时如果有任何疑问,可以与南通特洛菲饲料科技有限公司技术部咨询。

 

参考文献:

BT Thach, JP Kenney-Hunt, TC Simon, JL Stratman, SB Thach, KA Harris, S Saunders, JM Cheverud. Sex-specific quantitative trait loci linked to autoresuscitation failure in SWR/J mice. Heredity (Edinb). 2009 December; 103(6): 469–475. 

Oliver C. Turner, Robert G. Keefe, Isamu Sugawara, Hiroyuki Yamada, Ian M. Orme. SWR Mice Are Highly Susceptible to Pulmonary Infection with Mycobacterium tuberculosis. Infect Immun. 2003 September; 71(9): 5266–5272.

Xie S, Chang SH, Yang P, Jacob C, Kaliyaperumal A, Datta SK, Mohan C. Genetic contributions of nonautoimmune SWR mice to lupus nephritis. J Immunol. 2001;167:7141–7149 

Osman GE; Hannibal MC; Anderson JP; Cheunsuk S; Lasky SR; Liggitt HD; Ladiges WC; Hood LE. T-cell receptor vbeta deletion and valpha polymorphism are responsible for the resistance of SWR mouse to arthritis induction. Immunogenetics 1999, 49(9):764-72.

Fischer Lindahl K. . On naming H2 haplotypes: functional significance of MHC class Ib alleles. Immunogenetics 1997, 46(1):53-62.

Osman GE; Jacobson DP; Li SW; Hood LE; Liggitt HD; Ladiges WC.  SWR: an inbred strain suitable for generating transgenic mice. Lab Anim Sci 1997, 47(2):167-71.

Lindsey JW. Characteristics of initial and reinduced experimental autoimmune encephalomyelitis. Immunogenetics 1996, 44(4):292-7.

Kirk EA; Moe GL; Caldwell MT; Lernmark JA; Wilson DL; LeBoeuf RC. Hyper- and hypo-responsiveness to dietary fat and cholesterol among inbred mice: searching for level and variability genes. J Lipid Res 1995, 36(7):1522-32.

Paigen B. Genetics of responsiveness to high-fat and high- cholesterol diets in the mouse. Am J Clin Nutr 1995, 62(2):458S-462S.

Ortman RA; Holderbaum D; Qu XM; Banerjee S; Haqqi TM.  BUB/BnJ (H-2q) is a TCR deletion mutant mouse strain (TCR V beta a, KJ16-) that is susceptible to type II collagen-induced arthritis. J Immunol 1994, 152(8):4175-82.

Nishina PM; Wang J; Toyofuku W; Kuypers FA; Ishida BY; Paigen B. Atherosclerosis and plasma and liver lipids in nine inbred strains of mice. 1993, Lipids 28(7):599-605.

Reife RA, Loutis N, Watson WC, Hasty KA, Stuart JM. SWR mice are resistant to collagen-induced arthritis but produce potentially arthritogenic antibodies. Arthritis Rheum. 1991;34:776–81. 

Jiao S; Cole TG; Kitchens RT; Pfleger B; Schonfeld G.  Genetic heterogeneity of plasma lipoproteins in the mouse: control of low density lipoprotein particle sizes by genetic factors. J Lipid Res 1990, 31(3):467-77.

Paigen B; Ishida BY; Verstuyft J; Winters RB; Albee D. Atherosclerosis susceptibility differences among progenitors of recombinant inbred strains of mice. Arteriosclerosis 1990, 10(2):316-23.

Serreze DV; Leiter EH.  Defective activation of T suppressor cell function in nonobese diabetic mice. Potential relation to cytokine deficiencies. J Immunol 1988, 140(11):3801-7.

Beamer WG, Hoppe PC, Whitten WK. Spontaneous malignant granulosa cell tumors in ovaries of young SWR mice.Cancer Res. 1985 Nov;45(11 Pt 2):5575-81.  

Paigen B; Morrow A; Brandon C; Mitchell D; Holmes P. Variation in susceptibility to atherosclerosis among inbred strains of mice. Atherosclerosis 1985,57(1):65-73.

Shen FW; Chorney MJ; Boyse EA.  Further polymorphism of the Tla locus defined by monoclonal TL antibodies. Immunogenetics 1982,15(6):573-8.   

Kutscher CL; Miller M; Schmalbach NL. Renal deficiency associated with diabetes insipidus in the SWR/J mouse. Physiol Behav 1975, 14(6):815-8.

Kutscher CL; Schmalbach NL.  Effects of water deprivation, NaCl injection, and seven aversive taste stimuli on drinking in two normal mouse strains and one with diabetes insipidus. Physiol Behav 1975, 15(6):659-67.

Kutscher CL; Miller DG.  Age-dependent polydipsia in the SWR-J mouse. Physiol Behav 1974, 13(1):71-9.

Levine S; Sowinski R.  Experimental allergic encephalomyelitis in inbred and outbred mice. J Immunol 1973, 110(1):139-43.

Deringer MK.  Mammary tumors in strains BL-LyDe and SWR-LyDe mice. J Natl Cancer Inst 1970,45(2):215-8.

Lynch CJ. The so-called Swiss mouse. Lab Anim Care 1969, 19(2):214-20.



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