Nonhuman primate parthenogenetic stem cells

被引:123
作者
Vrana, KE
Hipp, JD
Goss, AM
McCool, BA
Riddle, DR
Walker, SJ
Wettstein, PJ
Studer, LP
Tabar, V
Cunniff, K
Chapman, K
Vilner, L
West, MD
Grant, KA
Cibelli, JB [1 ]
机构
[1] Wake Forest Univ, Sch Med, Dept Physiol & Pharmacol, Ctr Neurobehav Study Alcohol, Winston Salem, NC 27157 USA
[2] Wake Forest Univ, Sch Med, Dept Neurobiol & Anat, Winston Salem, NC 27157 USA
[3] Mayo Clin, Dept Microbiol & Immunol, Rochester, MN 55905 USA
[4] Mem Sloan Kettering Canc Ctr, New York, NY 10021 USA
[5] Adv Cell Technol, Worcester, MA 01605 USA
[6] Millennium Pharmaceut Inc, Cambridge, MA 02139 USA
[7] Michigan State Univ, Dept Anim Sci Physiol, E Lansing, MI 48824 USA
关键词
D O I
10.1073/pnas.2034195100
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Parthenogenesis is the biological phenomenon by which embryonic development is initiated without male contribution. Whereas parthenogenesis is a common mode of reproduction in lower organisms, the mammalian parthenote fails to produce a successful pregnancy. We herein describe in vitro parthenogenetic development of monkey (Macaca fascicularis) eggs to the blastocyst stage, and their use to create a pluripotent line of stem cells. These monkey stem cells (Cyno-1 cells) are positive for telomerase activity and are immunoreactive for alkaline phosphatase, octamer-binding transcription factor 4 (Oct-4), stage-specific embryonic antigen 4 (SSEA-4), tumor rejection antigen 1-60 (TRA 1-60), and tumor rejection antigen 1-81 (TRA 1-81) (traditional markers of human embryonic stem cells). They have a normal chromosome karyotype (40 + 2) and can be maintained in vitro in an undifferentiated state for extended periods of time. Cyno-1 cells can be differentiated in vitro into dopaminergic and serotonergic neurons, contractile cardiomyocyte-like cells, smooth muscle, ciliated epithelia, and adipocytes. When Cyno-1 cells were injected into severe combined immunodeficient mice, teratomas with derivatives from all three embryonic germ layers were obtained. When grown on fibronectin/laminin-coated plates and in neural progenitor medium, Cyno-1 cells assume a neural precursor phenotype (immunoreactive for nestin). However, these cells remain proliferative and express no functional ion channels. When transferred to differentiation conditions, the nestin-positive precursors assume neuronal and epithelial morphologies. Over time, these cells acquire electrophysiological characteristics of functional neurons (appearance of tetrodotoxin-sensitive, voltage-dependent sodium channels). These results suggest that stem cells derived from the parthenogenetically activated nonhuman primate egg provide a potential source for autologous cell therapy in the female and bypass the need for creating a competent embryo.
引用
收藏
页码:11911 / 11916
页数:6
相关论文
共 45 条
[1]  
ALLEN ND, 1994, DEVELOPMENT, V120, P1473
[2]  
ALTINTAS A, 1993, J IMMUNOL, V151, P2803
[3]   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
[4]  
[Anonymous], 1994, MANIPULATING MOUSE E
[5]   mTert expression correlates with telomerase activity during the differentiation of murine embryonic stem cells [J].
Armstrong, L ;
Lako, M ;
Lincoln, J ;
Cairns, PM ;
Hole, N .
MECHANISMS OF DEVELOPMENT, 2000, 97 (1-2) :109-116
[6]   Safety and tolerability assessment of intrastriatal neural allografts in five patients with Huntington's disease [J].
Bachoud-Lévi, AC ;
Bourdet, C ;
Brugières, P ;
Nguyen, JP ;
Grandmougin, T ;
Haddad, B ;
Jény, R ;
Bartolomeo, P ;
Boissé, MF ;
Dalla Barba, G ;
Degos, JD ;
Ergis, AM ;
Lefaucheur, JP ;
Lisovoski, F ;
Pailhous, E ;
Rémy, P ;
Palfi, S ;
Defer, GL ;
Cesaro, P ;
Hantraye, P ;
Peschanski, M .
EXPERIMENTAL NEUROLOGY, 2000, 161 (01) :194-202
[7]   Medical progress - Chorionic tumors [J].
Berkowitz, RS ;
Goldstein, DP .
NEW ENGLAND JOURNAL OF MEDICINE, 1996, 335 (23) :1740-1748
[8]  
Boediono A, 1999, MOL REPROD DEV, V53, P159, DOI 10.1002/(SICI)1098-2795(199906)53:2&lt
[9]  
159::AID-MRD5&gt
[10]  
3.0.CO