Jump to: Page Content, Section Navigation, Site Navigation, Site Search, Account Information, or Site Tools.
|
|
Technical CommentsResponse to Comment on "Molecular Correlates of Primate Nuclear Transfer Failures"Space constraints precluded publication of bovine nuclear transfer (NT) data (Fig. 1) that may allay the concerns of Lanza et al (1). After primate NT, disorganized spindles with chaotically distributed chromosomes are always observed (2). Bovine NTs, however, organize a single microtubule aster emanating from the juxtanuclear NT centrosome at first interphase (Fig. 1A). Mitotic bovine NTs frequently assemble symmetrical bipolar spindles with precisely aligned chromosomes [Fig. 1B, blue and (2)], a situation never observed after primate NT. These and centrosome and kinesin NT data are subjects of a forthcoming report (3).
Without benefit of this additional knowledge, Lanza et al. fairly raise the uncertainty in interpreting NT results, especially in extrapolating assisted reproductive technology (ART) successes or failures between species. For example, >90% fertilization is routinely achieved using intracytoplasmic sperm injection (ICSI) in both humans and nonhuman primates (resulting in the global adoption of ICSI by ART clinics), whereas ICSI has produced few mice or cattle (4). Because NT successes vary, comparisons between Dolly's birth after 29 embryo transfers into 13 ewes (5) and our lack of established pregnancies after 33 rhesus embryo transfers are not reasonable. Primate ART, including NT, is uniquely challenging (6): Oocyte availability and quality, synchronized surrogates, cleavage-stage embryo transfers versus blastocysts transfers, and reproductive seasonality all present practical limitations. And unlike mice and domestic mammals, primates carry singletons. Finally, while the protocols for mouse and bovine NT are species-specific, primate laboratories must extrapolate from human ART clinics for simian-specific optimizations. Although human embryonic stem cells (hESCs) derived after NT might overcome immune rejection, NT epigenetic abnormalities (7) and microchimerism in transplantation patients (8) encourage alternate strategies for tolerance or managing incompatibilities. In light of the available evidence, we maintain our original conclusion (2) that "[w]ith current approaches, [primate] NT to produce embryonic stem cells may prove difficultand reproductive cloning unachievable." We agree with Lanza et al. (1) that interpretations regarding both NT and hESC data in primates, human (9, 10) and nonhuman (5, 11) alike, should be "tempered with abundant caution."
References
Received for publication 9 June 2003. Accepted for publication 8 August 2003.
The editors suggest the following Related Resources on Science sites:In Science Magazine
|
Science. ISSN 0036-8075 (print), 1095-9203 (online)