Evidence map›Paper›PMID 40747959›Full record

ArticleProteomics2025

Dynamic Proteome Landscape During Preimplantation Human Embryo Development and Trophectoderm Stem Cell-Differentiation.

Alin Rai, Qi Hui Poh, Hiroaki Okae, Takahiro Arima, Mehdi Totonchi, David W Greening

Abstract read
In one paragraph

Article in Proteomics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. An Integrated Proteomics and Genomics Approach to Identify Essential Protein Kinases During Human Trophoblast Development.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
  2. Ultra-low oxygen tension duringbioRxiv : the preprint server for biology · 2026
    Article
  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Alin RaiBaker Heart and Diabetes Institute, Melbourne, Victoria, Australia.
Qi Hui PohBaker Heart and Diabetes Institute, Melbourne, Victoria, Australia.ORCID 0000-0003-2620-2834
Hiroaki OkaeDepartment of Informative Genetics, Environment and Genome Research Center, Tohoku University Graduate School of Medicine, Sendai, Japan.
Takahiro ArimaDepartment of Informative Genetics, Environment and Genome Research Center, Tohoku University Graduate School of Medicine, Sendai, Japan.
Mehdi TotonchiDepartment of Genetics, Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran.
David W GreeningBaker Heart and Diabetes Institute, Melbourne, Victoria, Australia.ORCID 0000-0001-7516-485X

Funding

Baker Institute-La Trobe University Research Training Program ScholarshipFuture Fund 1201805Helen Amelia Hains FellowshipNational Health and Medical Research Council Project 1057741National Health and Medical Research Council Project 1139489Victorian State Government Operational Infrastructure
6 · The paper itself

Abstract

Embryo development involves fertilization of a mature ovum, which, after sequential cell divisions (2-,4-8-cells and morula), undergoes differentiation into implantation competent blastocyst. The blastocyst comprises of inner cell mass surrounded by an outer layer of cells called the trophoblast (TSblast) that, upon attachment to the endometrium, differentiates into extravillous trophoblasts (EVTs) that facilitates embryo invasion into the endometrium for intrauterine embryo development, and syncytiotrophoblast (ST) that form the placenta. Such cellular differentiation stages are critical for embryogenesis and implantation, although the protein expression landscape remains poorly understood in humans. Using quantitative mass spectrometry analysis, we systematically monitored the protein expression landscape and their dynamic regulation between human ovum (M2), 8-cell embryo, and blastocysts stages, and trophoblast lineage-specific differentiation into EVTs and ST. Proteins temporally regulated from M2-8 cell-blastocyst stage displayed significant enrichment for metabolic protein networks. We specifically identified 156 proteins associated with 8-cell embryos to blastocyst development, 54 displayed similar correlation at the transcriptomic level including mitochondrial, junction/secretory granule-associated proteins that carry glycolytic, antioxidant, and telomerase maintenance functions. We reveal a striking lineage-specific reprogramming of TSblast proteome during fate-specification. These findings extend our knowledge of the sequential order of protein landscape reprogramming and processes during early human embryogenesis and trophoblast function. SUMMARY: Although genomic and transcriptomic studies have provided key understanding of the genetic programs underlying preimplantation embryo development, the protein expression landscape remains unexplored. Here, a quantitative proteomic study of human preimplantation embryo stages reveal a dynamic proteome landscape from M2, 8-cell, and blastocyst stage, and during trophoblast stem cell (TS) differentiation. Identified key factors in early human embryos and lineage-specific trophoblast proteome profiles, further correlated with transcriptomic analyses. This direct proteomic analysis provides a quantitative and temporal analysis of the dynamic protein expression in human embryos during preimplantation development and a powerful resource to enable further mechanistic studies on human trophoblast development and function.

Indexed as

BlastocystCell DifferentiationEmbryonic DevelopmentProteomeTrophoblastsFemaleHumansPregnancyProteomicsProteomeblastocysthuman embryoproteomicsreproductionstem cellstrophoblasts

Identifiers

PMID40747959
PMCPMC12329398

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.