Rauner Gat, Barash Itamar
Institute of Animal Science, ARO, The Volcani Center, P.O. Box 6, Bet-Dagan, 50250, Israel; The Robert H. Smith Faculty of Agriculture, Food and Environment, The Hebrew University of Jerusalem, Israel.
Institute of Animal Science, ARO, The Volcani Center, P.O. Box 6, Bet-Dagan, 50250, Israel.
Exp Cell Res. 2014 Oct 15;328(1):186-196. doi: 10.1016/j.yexcr.2014.06.017. Epub 2014 Jun 30.
The challenge in manipulating the proportion of somatic stem cells lies in having to override tissue homeostasis. Xanthosine infusion via the teat canal has been reported to augment the number of label-retaining cells in the mammary gland of 3-month-old bovine calves. To further delineate xanthosine׳s effect on defined stem cells in the mammary gland of heifers-which are candidates for increased prospective milk production following such manipulation-bovine mammary parenchymal tissue was transplanted and integrated into the cleared mammary fat pad of immunodeficient mice. Xanthosine administration for 14 days did not affect the number of label-retaining cells after 10- and 11-week chases. No change in stem cell proportion, analyzed according to CD49f and CD24 expression, was noted. Clone formation and propagation rate of cultured cells, as well as expression of stem cell markers, were also unaffected. In contrast, a latent 50% decrease in bovine mammary cell proliferation rate was observed 11 weeks after xanthosine administration. Tumor development in mice was also limited by xanthosine administration. These effects may have resulted from an initial decrease in expression of the rate-limiting enzyme in guanine synthesis, IMPDH. The data indicate that caution should be exerted when considering xanthosine for stem cell manipulation.
操纵体干细胞比例的挑战在于必须打破组织稳态。据报道,通过乳头管注入黄苷可增加3月龄犊牛乳腺中标记保留细胞的数量。为了进一步阐明黄苷对小母牛乳腺中特定干细胞的影响(这些小母牛是经过此类操作后预期产奶量增加的候选对象),将牛乳腺实质组织进行移植,并整合到免疫缺陷小鼠清除后的乳腺脂肪垫中。在进行10周和11周的追踪后,给予黄苷14天并未影响标记保留细胞的数量。根据CD49f和CD24表达分析,干细胞比例没有变化。培养细胞的克隆形成和增殖率以及干细胞标志物的表达也未受影响。相比之下,在给予黄苷11周后,观察到牛乳腺细胞增殖率潜在下降了50%。给予黄苷也限制了小鼠肿瘤的发展。这些影响可能是由于鸟嘌呤合成限速酶IMPDH的表达最初下降所致。数据表明,在考虑将黄苷用于干细胞操纵时应谨慎行事。