Evidence map›Paper›PMID 20553595›Full record

ArticleBMC systems biology2010

Hematopoietic differentiation: a coordinated dynamical process towards attractor stable states.

Nadia Felli, Luciano Cianetti, Elvira Pelosi, Alessandra Carè, Chang Gong Liu, George A Calin, Simona Rossi, Cesare Peschle, Giovanna Marziali, Alessandro Giuliani

Abstract read
In one paragraph

Article in BMC systems biology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

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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

10 citing papers in PubMed.

  1. Network Analysis of miRNA and Cytokine Landscape in Human Hematopoiesis.International journal of molecular sciences · 2024
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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

10 authors.

Nadia FelliDepartment of Hematology, Oncology and Molecular Medicine Istituto Superiore di Sanità, Rome, Italy.
Luciano Cianetti
Elvira Pelosi
Alessandra Carè
Chang Gong Liu
George A Calin
Simona Rossi
Cesare Peschle
Giovanna Marziali
Alessandro Giuliani

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe differentiation process, proceeding from stem cells towards the different committed cell types, can be considered as a trajectory towards an attractor of a dynamical process. This view, taking into consideration the transcriptome and miRNome dynamics considered as a whole, instead of looking at few 'master genes' driving the system, offers a novel perspective on this phenomenon. We investigated the 'differentiation trajectories' of the hematopoietic system considering a genome-wide scenario.

resultsWe developed serum-free liquid suspension unilineage cultures of cord blood (CB) CD34+ hematopoietic progenitor cells through erythroid (E), megakaryocytic (MK), granulocytic (G) and monocytic (Mo) pathways. These cultures recapitulate physiological hematopoiesis, allowing the analysis of almost pure unilineage precursors starting from initial differentiation of HPCs until terminal maturation. By analyzing the expression profile of protein coding genes and microRNAs in unilineage CB E, MK, G and Mo cultures, at sequential stages of differentiation and maturation, we observed a coordinated, fully interconnected and scalable character of cell population behaviour in both transcriptome and miRNome spaces reminiscent of an attractor-like dynamics. MiRNome and transcriptome space differed for a still not terminally committed behaviour of microRNAs.

conclusionsConsistent with their roles, the transcriptome system can be considered as the state space of a cell population, while the continuously evolving miRNA space corresponds to the tuning system necessary to reach the attractor. The behaviour of miRNA machinery could be of great relevance not only for the promise of reversing the differentiated state but even for tumor biology.

Indexed as

Models, BiologicalAntigens, CD34Cell Culture TechniquesCell DifferentiationCell LineageComputational BiologyFetal BloodFlow CytometryGene Expression ProfilingGenomeHematopoietic Stem CellsOligonucleotide Array Sequence AnalysisSignal TransductionAntigens, CD34

Identifiers

PMID20553595
PMCPMC2904736

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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.