Organoid generation from trophoblast stem cells highlights distinct roles for cytotrophoblasts and stem cells in organoid formation and expansion.

IF 3 2区 医学 Q2 DEVELOPMENTAL BIOLOGY Placenta Pub Date : 2024-12-05 DOI:10.1016/j.placenta.2024.12.003
Cherry Sun, Lawrence W Chamley, Joanna L James
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Abstract

Background: Organoids are stem-cell derived, self-organised, three-dimensional cultures that improve in vitro recapitulation of tissue structure. The generation of trophoblast organoids using primary placental villous digests (containing cytotrophoblasts and trophoblast stem cells (TSC)) improved high-throughput assessment of early trophoblast differentiation. However, the relative contributions of cytotrophoblasts and TSCs to trophoblast organoid growth and differentiation remain unclear, with implications for model interpretation. Here we sought to generate organoids from side-population trophoblasts (SpTSCs) to better understand the contribution of TSC to trophoblast organoid formation.

Methods: Methods were adapted from Haider et al., 2018 to generate organoids from Okae TSCs (OkTSCs) or SpTSCs. Organoid growth was compared with primary villous trophoblast organoids and cellular composition interrogated by immunohistochemistry.

Results: Organoids can be derived from first-trimester SpTSCs that exhibit similar architecture to those from primary villous trophoblast. However, organoids established from pure TSC populations (OkTSC or SpTSC) have different growth dynamics to primary placental villous digest-derived organoids - with OkTSCs developing faster and spontaneously generating migratory cells, whilst SpTSC organoids grow more slowly. Importantly, depletion of SpTSC from first-trimester villous digests ablates organoid formation. Finally, the capacity of the side-population technique to isolate late-gestation TSC enabled the generation of trophoblast organoids from term placentae, although these were significantly smaller than their first-trimester SpTSC counterparts.

Discussion: Together, this work highlights the requirement of TSC for organoid formation, and the functional distinction between TSC and cytotrophoblasts. Proof-of-principle data demonstrating organoid generation from late gestation TSC isolated directly from the placenta lays the groundwork for future disease models.

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从滋养层干细胞生成类器官突出了细胞滋养层细胞和干细胞在类器官形成和扩增中的不同作用。
背景:类器官是干细胞衍生的、自组织的、三维培养的,可以改善组织结构的体外再现。利用原代胎盘绒毛消化(含有细胞滋养细胞和滋养细胞干细胞(TSC))产生滋养细胞类器官,提高了对早期滋养细胞分化的高通量评估。然而,细胞滋养层细胞和TSCs对滋养层细胞类器官生长和分化的相对贡献尚不清楚,这对模型解释有影响。为了更好地了解TSC对滋养层细胞类器官形成的贡献,我们试图从侧群滋养层细胞(SpTSCs)中生成类器官。方法:采用Haider et al., 2018的方法,从Okae TSCs (OkTSCs)或SpTSCs中生成类器官。类器官生长与原代绒毛滋养细胞进行比较,并通过免疫组化研究细胞组成。结果:类器官可以从妊娠早期的SpTSCs中获得,其结构与原代绒毛滋养细胞相似。然而,从纯TSC群体(OkTSC或SpTSC)建立的类器官与原代胎盘绒毛消化来源的类器官具有不同的生长动力学- OkTSC发育更快并自发产生迁移细胞,而SpTSC类器官生长较慢。重要的是,早孕期绒毛消化过程中SpTSC的消耗会破坏类器官的形成。最后,侧群体技术分离妊娠晚期TSC的能力使足月胎盘产生滋养细胞类器官,尽管这些器官明显小于妊娠早期的SpTSC。总之,这项工作强调了TSC对类器官形成的要求,以及TSC和细胞滋养细胞之间的功能区别。原理验证数据表明,直接从胎盘分离的妊娠晚期TSC可产生类器官,这为未来的疾病模型奠定了基础。
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来源期刊
Placenta
Placenta 医学-发育生物学
CiteScore
6.30
自引率
10.50%
发文量
391
审稿时长
78 days
期刊介绍: Placenta publishes high-quality original articles and invited topical reviews on all aspects of human and animal placentation, and the interactions between the mother, the placenta and fetal development. Topics covered include evolution, development, genetics and epigenetics, stem cells, metabolism, transport, immunology, pathology, pharmacology, cell and molecular biology, and developmental programming. The Editors welcome studies on implantation and the endometrium, comparative placentation, the uterine and umbilical circulations, the relationship between fetal and placental development, clinical aspects of altered placental development or function, the placental membranes, the influence of paternal factors on placental development or function, and the assessment of biomarkers of placental disorders.
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