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Normal reproductive and macrophage function in Pem homeobox gene-deficient mice

机译:Pem同源异型框基因缺陷小鼠的正常生殖和巨噬细胞功能

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摘要

Interaction between germ cells and the supporting somatic cells guides many of the differentiative processes of gametogenesis. The expression pattern of the Pem homeobox gene suggests that it may mediate specific inductive events in murine reproductive tissues. During gestation, Pem is expressed in migrating and early postmigratory primordial germ cells, as well as in all embryo-derived extraembryonic membranes. Pem expression ceases in the germline after Embryonic Day 14 in both sexes and then reappears postnatally in the supporting cells of the gonad. In mature mice, Pem is produced by testicular Sertoli cells during stages VI-VIII of spermatogenesis and transiently by ovarian granulosa cells lining periovulatory follicles. Despite this tightly regulated reproductive expression pattern, mice with a targeted mutation in Pem have normal fecundity, with no detectable alteration in extraembryonic testicular or ovarian development or function, We also show that Pem is expressed throughout embryonic and adult development in a subset of a tissue-specific class of macrophages, Kupffer cells, as well as in a localized fraction of cells in macrophage cell lines, Although the number of Pem-positive Kupffer cells increases in mice treated with lipopolysaccharide, loss of Pem does not detectably interfere with the cells' ability to induce iNOS expression, demonstrating this Kupffer cell function does not require Fern. No differences were observed between Pem-knockout mice in 129, C57BL6/J, or mixed genetic backgrounds. Together, these data show that Pem is dispensable for embryonic and postnatal development, gonadal function, and Kupffer cell activation, perhaps due. to compensatory expression of a similar homeobox gene. (C) 1998 Academic Press. [References: 80]
机译:生殖细胞和支持体细胞之间的相互作用指导了配子发生的许多分化过程。 Pem同源盒基因的表达模式表明它可能介导小鼠生殖组织中的特定诱导事件。在妊娠期间,Pem在迁移的和迁移后的原始原始生殖细胞以及所有胚胎衍生的胚外膜中表达。在胚胎的第14天后,两性中的Pem表达均停止在生殖系中,然后在产后的性腺支持细胞中重新出现。在成年小鼠中,Pem是由睾丸支持细胞在精子发生的第VI-VIII阶段产生的,并由排卵性卵泡排列的卵巢颗粒细胞产生的。尽管这种生殖表达模式受到严格控制,但具有Pem靶向突变的小鼠仍具有正常的繁殖力,胚胎外睾丸或卵巢发育或功能没有可检测到的改变。巨噬细胞,库普弗细胞以及巨噬细胞系中局部细胞的特定类别,尽管用脂多糖处理的小鼠中Pem阳性库普弗细胞的数量增加,但Pem的损失不会明显干扰细胞的诱导iNOS表达的能力,证明这种库普弗细胞功能不需要Fern。在129,C57BL6 / J或混合遗传背景下的Pem基因敲除小鼠之间未观察到差异。总之,这些数据表明,Pem对于胚胎和出生后的发育,性腺功能和库普弗细胞活化可能是必需的。补偿类似同源盒基因的表达。 (C)1998年学术出版社。 [参考:80]

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