Establishment of an embryonic stem (ES) cell line derived from a non-obese diabetic (NOD) mouse: in vivo differentiation into lymphocytes and potential for germ line transmission

被引:28
作者
Nagafuchi, S
Katsuta, H
Kogawa, K
Akashi, T
Kondo, S
Sakai, Y
Tsukiyama, T
Kitamura, D
Niho, Y
Watanabe, T
机构
[1] Kyushu Univ, Med Inst Bioregulat, Sch Hlth Sci, Dept Med Technol,Higashi Ku, Fukuoka 8128582, Japan
[2] Kyushu Univ, Med Inst Bioregulat, Dept Internal Med 1, Fukuoka 8128582, Japan
[3] Kyushu Univ, Dept Mol Immunol, Fukuoka 8128582, Japan
[4] Kyushu Univ, Med Inst Bioregulat, Dept Mol & Cellular Biol, Fukuoka 8128582, Japan
[5] Sci Univ Tokyo, Res Inst Biol Sci, Div Mol Biol, Noda, Chiba 278, Japan
关键词
embryonic stem cell; non-obese diabetic mouse; germ line transmission; diabetes; insulitis;
D O I
10.1016/S0014-5793(99)00801-7
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
A non-obese diabetic (NOD) mouse-derived embryonic stem (ES) cell line has been stably maintained in an undifferentiated state with a characteristic ES cell-like morphology, expressing the stem cell marker alkaline phosphatase, and displaying a normal diploid karyotype, After injecting the NODES cells into blastocysts, chimeric mice were obtained. Small but significant numbers of lymphocytes expressed the NOD-derived MHC allele, When a chimeric mouse was mated with C57BL/6 mice, an agouti mouse was obtained, having the NOD-derived H-2 I-A(beta)(g7) haplotype. Thus, an NOD-ES cell line which cao differentiate into lymphocytes with potential for germ line transmission was successfully established. (C) 1999 Federation of European Biochemical Societies.
引用
收藏
页码:101 / 104
页数:4
相关论文
共 30 条
[1]   Direct evidence for the contribution of B cells to the progression of insulitis and the development of diabetes in non-obese diabetic mice [J].
Akashi, T ;
Nagafuchi, S ;
Anzai, K ;
Kondo, S ;
Kitamura, D ;
Wakana, S ;
Ono, J ;
Kikuchi, M ;
Niho, Y ;
Watanabe, T .
INTERNATIONAL IMMUNOLOGY, 1997, 9 (08) :1159-1164
[2]   INSULIN-DEPENDENT DIABETES-MELLITUS AS A BETA-CELL TARGETED DISEASE OF IMMUNOREGULATION [J].
BACH, JF .
JOURNAL OF AUTOIMMUNITY, 1995, 8 (04) :439-463
[3]  
BENDELAC AC, 1987, J EXP MED, V16, P823
[4]   FORMATION OF GERM-LINE CHIMERAS FROM EMBRYO-DERIVED TERATOCARCINOMA CELL-LINES [J].
BRADLEY, A ;
EVANS, M ;
KAUFMAN, MH ;
ROBERTSON, E .
NATURE, 1984, 309 (5965) :255-256
[5]   ADOPTIVE TRANSFER OF DIABETES INTO IMMUNODEFICIENT NOD-SCID SCID MICE - RELATIVE CONTRIBUTIONS OF CD4+ AND CD8+ T-CELLS FROM DIABETIC VERSUS PREDIABETIC NOD.NON-THY-1A DONORS [J].
CHRISTIANSON, SW ;
SHULTZ, LD ;
LEITER, EH .
DIABETES, 1993, 42 (01) :44-55
[6]   The nonobese diabetic mouse as a model of autoimmune diabetes: Immune dysregulation gets the NOD [J].
Delovitch, TL ;
Singh, B .
IMMUNITY, 1997, 7 (06) :727-738
[7]   ESTABLISHMENT IN CULTURE OF PLURIPOTENTIAL CELLS FROM MOUSE EMBRYOS [J].
EVANS, MJ ;
KAUFMAN, MH .
NATURE, 1981, 292 (5819) :154-156
[8]  
Fox CJ, 1997, J IMMUNOL, V158, P2414
[9]   TRANSGENESIS BY MEANS OF BLASTOCYST-DERIVED EMBRYONIC STEM-CELL LINES [J].
GOSSLER, A ;
DOETSCHMAN, T ;
KORN, R ;
SERFLING, E ;
KEMLER, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (23) :9065-9069
[10]   HPRT-DEFICIENT (LESCH-NYHAN) MOUSE EMBRYOS DERIVED FROM GERMLINE COLONIZATION BY CULTURED-CELLS [J].
HOOPER, M ;
HARDY, K ;
HANDYSIDE, A ;
HUNTER, S ;
MONK, M .
NATURE, 1987, 326 (6110) :292-295