Smith Gilbert H
Basic Research Laboratory, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bldg. 37, Rm. 1122A, 37 Convent Drive, Bethesda, MD, 20892, USA.
J Mammary Gland Biol Neoplasia. 2016 Jun;21(1-2):21-3. doi: 10.1007/s10911-016-9356-5. Epub 2016 Jun 2.
In a recent paper (Rios et al. Nat Commun. 7:11400, 2016), it was reported that polyploid cells are frequent in lactating mammary tissues. This phenomenon was observed in mammary tissue sampled from five separate mammalian species. According to that report, these binucleated cells occur late in pregnancy and early in lactation. Unfortunately, this paper did not mention a number of earlier observations and findings that remain pertinent to this day (Banerjee et al. Life sciences Pt 2: Biochemistry, general and molecular biology. 10(15):867-77, 1971; Banerjee MR, Wagner JE. Biochem. Biophys. Res. Commun. 49(2):480-7, 1972). In these classical experiments, the authors demonstrated in vivo that DNA synthesis continued without commensurate cell division during late pregnancy and lactation, and that this DNA synthesis was imperative for functional differentiation of the mammary epithelium. Later studies showed that DNA synthesis was indispensable to the induction of milk protein production in explant cultures of mammary tissue from unprimed, nulliparous mice. This dependence on DNA synthesis in mammary explant cultures stimulated by lactogenic hormones was found to be dispensable following a single pregnancy. The absolute requirement for DNA synthesis in nulliparous mouse mammary explants stimulated to synthesize milk protein in vitro has remained unexplained, as has the need for DNA synthesis prior to the onset of lactation. From a historical perspective, it is more likely that binuclear secretory cells in the lactating mammary gland are a consequence of the DNA synthesis requirement for lactation, rather than an essential element.
在最近一篇论文(里奥斯等人,《自然通讯》,2016年,第7卷,第11400页)中,据报道多倍体细胞在哺乳期乳腺组织中很常见。在从五个不同哺乳动物物种采集的乳腺组织中观察到了这种现象。根据该报告,这些双核细胞出现在妊娠后期和哺乳早期。遗憾的是,这篇论文没有提及一些至今仍相关的早期观察结果和发现(巴纳吉等人,《生命科学》第2部分:生物化学、普通和分子生物学,1971年,第10卷,第15期,第867 - 877页;巴纳吉MR、瓦格纳JE,《生物化学与生物物理研究通讯》,1972年,第49卷,第2期,第480 - 487页)。在这些经典实验中,作者在体内证明,在妊娠后期和哺乳期,DNA合成持续进行,但细胞分裂并未相应增加,并且这种DNA合成对于乳腺上皮的功能分化至关重要。后来的研究表明,在未受孕的未育小鼠乳腺组织的外植体培养物中,DNA合成对于诱导乳蛋白产生是不可或缺的。发现在单次妊娠后,催乳激素刺激的乳腺外植体培养物中对DNA合成的这种依赖性是可以消除的。未受孕小鼠乳腺外植体在体外被刺激合成乳蛋白时对DNA合成的绝对需求以及泌乳开始前对DNA合成的需求一直未得到解释。从历史角度来看,哺乳期乳腺中的双核分泌细胞更有可能是泌乳对DNA合成需求的结果,而不是一个必需元素。