Institute for Reproduction and Perinatal Research, Department of Pathology & Laboratory Medicine, University of Kansas Medical Center, Kansas City, KS, United States of America.
Institute for Reproduction and Perinatal Research, Department of Pathology & Laboratory Medicine, University of Kansas Medical Center, Kansas City, KS, United States of America; Departments of Pediatrics and Obstetrics and Gynecology, University of Kansas Medical Center, Kansas City, KS, United States of America; Center for Perinatal Research, Children's Mercy Research Institute, Children's Mercy, Kansas City, MO, United States of America.
Biochim Biophys Acta Gen Subj. 2021 Jun;1865(6):129867. doi: 10.1016/j.bbagen.2021.129867. Epub 2021 Feb 5.
The placenta is formed by the coordinated expansion and differentiation of trophoblast stem (TS) cells along a multi-lineage pathway. Dynamic regulation of histone 3 lysine 9 (H3K9) methylation is pivotal to cell differentiation for many cell lineages, but little is known about its involvement in trophoblast cell development.
Expression of H3K9 methyltransferases was surveyed in rat TS cells maintained in the stem state and following differentiation. The role of suppressor of variegation 3-9 homolog 2 (SUV39H2) in the regulation of trophoblast cell lineage development was investigated using a loss-of-function approach in rat TS cells and ex vivo cultured rat blastocysts.
Among the twelve-known H3K9 methyltransferases, only SUV39H2 exhibited robust differential expression in stem versus differentiated TS cells. SUV39H2 transcript and protein expression were high in the stem state and declined as TS cells differentiated. Disruption of SUV39H2 expression in TS cells led to an arrest in TS cell proliferation and activation of trophoblast cell differentiation. SUV39H2 regulated H3K9 methylation status at loci exhibiting differentiation-dependent gene expression. Analyses of SUV39H2 on ex vivo rat blastocyst development supported its role in regulating TS cell expansion and differentiation. We further identified SUV39H2 as a downstream target of caudal type homeobox 2, a master regulator of trophoblast lineage development.
Our findings indicate that SUV39H2 contributes to the maintenance of TS cells and restrains trophoblast cell differentiation.
SUV39H2 serves as a contributor to the epigenetic regulation of hemochorial placental development.
胎盘是由滋养层干细胞(TS)沿着多谱系途径协调扩张和分化形成的。组蛋白 3 赖氨酸 9(H3K9)甲基化的动态调控对许多细胞谱系的细胞分化至关重要,但对滋养细胞发育中 H3K9 甲基化的参与知之甚少。
在维持在干细胞状态和分化后的大鼠 TS 细胞中,调查 H3K9 甲基转移酶的表达。在大鼠 TS 细胞和体外培养的大鼠囊胚中采用功能丧失方法,研究 SUV39H2 同源物 2(SUV39H2)在滋养细胞谱系发育中的调节作用。
在 12 种已知的 H3K9 甲基转移酶中,只有 SUV39H2 在干细胞与分化的 TS 细胞中表现出强烈的差异表达。SUV39H2 转录本和蛋白表达在干细胞状态下较高,随着 TS 细胞分化而下降。TS 细胞中 SUV39H2 表达的破坏导致 TS 细胞增殖停滞和滋养细胞分化激活。SUV39H2 调节在分化依赖性基因表达中表现出 H3K9 甲基化状态。对 SUV39H2 在体外大鼠囊胚发育中的分析支持其在调节 TS 细胞扩增和分化中的作用。我们进一步确定 SUV39H2 是尾型同源盒 2 的下游靶标,尾型同源盒 2 是滋养层谱系发育的主要调节因子。
我们的发现表明 SUV39H2 有助于维持 TS 细胞并抑制滋养细胞分化。
SUV39H2 是合胞滋养层胎盘发育的表观遗传调控的贡献者。