Organized development from human embryonic stem cells after injection into immunodeficient mice

被引:48
作者
Gertow, K [1 ]
Wolbank, S
Rozell, B
Sugars, R
Andäng, M
Parish, CL
Imreh, MP
Wendel, M
Ährlund-Richter, L
机构
[1] Karolinska Inst, MBB, Dept Lab Med, Clin Res Ctr, S-14157 Stockholm, Sweden
[2] Karolinska Inst, MBB, Dept Lab Med, Div Pathol, S-14157 Stockholm, Sweden
[3] Karolinska Inst, MBB, Ctr Oral Biol, S-14157 Stockholm, Sweden
[4] Karolinska Inst, MBB, Mol Neurobiol Unit, S-14157 Stockholm, Sweden
关键词
D O I
10.1089/1547328041797499
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Information concerning the development and differentiation of human embryonic stem (hES) cells in vivo is limited. The present study has focused on the in vivo outcome and differentiation of the hESC line HS181, after injection into SCID/beige mice. hES cell-derived teratomas were explored using histological evaluation and by the identification of markers for differentiated cells and tissues. The analyses identified predominant differentiation along a neuronal lineage, the formation of bone/cartilage and epithelia. Fluorescent in situ hybridization ( FISH) analysis with a human-specific probe showed the teratomas to be mainly of human origin, with the most organized areas being exclusively human. Importantly, the study revealed interactions between mouse and human tissues, most notably in the formation of vessels. Both mouse and human cells contributed to specific microstructures in which mouse cells could be observed to take on the appropriate histiotypic appearance. Hence, HS181 cells were able to develop into defined mature tissues, supporting the relevant use of this hES cells model for studies of early human development, given the use of appropriate controls for host contribution. Although extensive mitotic activity implicated progenitor cell activity, no detectable multipotent or malignant areas were observed during the observation period. Persisting undifferentiated hESC were not detected.
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页码:421 / 435
页数:15
相关论文
共 39 条
[1]   Clonally derived human embryonic stem cell lines maintain pluripotency and proliferative potential for prolonged periods of culture [J].
Amit, M ;
Carpenter, MK ;
Inokuma, MS ;
Chiu, CP ;
Harris, CP ;
Waknitz, MA ;
Itskovitz-Eldor, J ;
Thomson, JA .
DEVELOPMENTAL BIOLOGY, 2000, 227 (02) :271-278
[2]   From teratocarcinomas to embryonic stem cells [J].
Andrews, PW .
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 2002, 357 (1420) :405-417
[3]   Early nephron formation in the developing mouse kidney [J].
Bard, JBL ;
Gordon, A ;
Sharp, L ;
Sellers, WI .
JOURNAL OF ANATOMY, 2001, 199 :385-392
[4]   EXPRESSION AND LOCALIZATION OF THE 2 SMALL PROTEOGLYCANS BIGLYCAN AND DECORIN IN DEVELOPING HUMAN SKELETAL AND NONSKELETAL TISSUES [J].
BIANCO, P ;
FISHER, LW ;
YOUNG, MF ;
TERMINE, JD ;
ROBEY, PG .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1990, 38 (11) :1549-1563
[5]  
BYRNE C, 1994, DEVELOPMENT, V120, P2369
[6]   Surface antigens of human embryonic stem cells: changes upon differentiation in culture [J].
Draper, JS ;
Pigott, C ;
Thomson, JA ;
Andrews, PW .
JOURNAL OF ANATOMY, 2002, 200 (03) :249-258
[7]   Development of melanocyte precursors from the vertebrate neural crest [J].
Dupin, E ;
Le Douarin, NM .
ONCOGENE, 2003, 22 (20) :3016-3023
[8]  
Fang JM, 1999, INT J DEV BIOL, V43, P335
[9]   NEURAL CELL-ADHESION MOLECULE (NCAM) IN ADULT VERTEBRATE RETINAS - TISSUE LOCALIZATION AND EVIDENCE AGAINST ITS ROLE IN RETINA PIGMENT-EPITHELIUM ADHESION [J].
FLIESLER, SJ ;
COLE, GJ ;
ADLER, AJ .
EXPERIMENTAL EYE RESEARCH, 1990, 50 (05) :475-482
[10]   Bone sialoprotein [J].
Ganss, B ;
Kim, RH ;
Sodek, J .
CRITICAL REVIEWS IN ORAL BIOLOGY & MEDICINE, 1999, 10 (01) :79-98