Stadtmauer Daniel J, Wagner Günter P
Department of Ecology and Evolutionary Biology, Yale Universisty. 165 Prospect Street, New Haven, CT, USA; Yale Systems Biology Institute, Yale University. 850 West Campus Drive, West Haven, CT, USA.
Department of Ecology and Evolutionary Biology, Yale Universisty. 165 Prospect Street, New Haven, CT, USA; Yale Systems Biology Institute, Yale University. 850 West Campus Drive, West Haven, CT, USA; Department of Obstetrics, Gynecology and Reproductive Sciences, Yale School of Medicine. 300 Cedar Street, New Haven, CT, USA; Department of Obstetrics and Gynecology, Wayne State University. 540 East Canfield Avenue, Detroit, MI, USA.
J Reprod Immunol. 2020 Feb;137:102626. doi: 10.1016/j.jri.2019.102626. Epub 2019 Oct 25.
The evolution of viviparity in therian mammals, i.e. marsupials and "placental" mammals, occurred by retention of the conceptus in the female reproductive tract and precocious "hatching" from the shell coat. Both eutherian embryo implantation and the opossum embryo attachment reaction are evolutionarily derived from and homologous to a defensive inflammatory process induced after shell coat hatching. However, both lineages, marsupials and placental mammals, have modified the inflammatory response substantially. We review the induction, maintenance, and effects of inflammation throughout pregnancy, with special attention to the role of prostaglandins and the mucosal inflammatory response, both of which likely had roles in early mammalian viviparity. We propose that the key step was not only suppression of the inflammatory response after implantation in placental mammals, but also the transfer of the inflammatory cell-cell communication network to a different set of cell types than in generic inflammation. To support this conclusion we discuss evidence that pro-inflammatory signal production in the opossum is not limited to maternal cells, as expected in bona fide defensive inflammation, but also includes fetal tissues, in a process we term cooperative inflammation. The ways in which the inflammatory reaction was independently modified in these two lineages helps explain major life history differences between extant marsupials and eutherians.
有袋类哺乳动物和“胎盘类”哺乳动物(即兽亚纲哺乳动物)的胎生进化过程,是通过将受精卵保留在雌性生殖道内并从卵壳中提前“孵化”来实现的。真兽类胚胎着床和负鼠胚胎附着反应在进化上均源自卵壳孵化后诱导的防御性炎症过程,且与之同源。然而,有袋类和胎盘类哺乳动物这两个谱系都对炎症反应进行了重大改变。我们回顾了整个孕期炎症的诱导、维持及影响,特别关注前列腺素的作用和黏膜炎症反应,这两者可能在早期哺乳动物胎生过程中都发挥了作用。我们提出,关键步骤不仅在于胎盘类哺乳动物着床后炎症反应的抑制,还在于将炎症细胞间通讯网络转移至与一般炎症不同的另一组细胞类型。为支持这一结论,我们讨论了相关证据,即负鼠体内促炎信号的产生并不局限于母体细胞(如真正的防御性炎症中所预期的那样),还包括胎儿组织,我们将这一过程称为协同炎症。这两个谱系中炎症反应的独立改变方式,有助于解释现存有袋类动物和真兽类动物在主要生活史方面的差异。