Evidence map›Paper›PMID 23791645›Full record

ArticleImmunity2013

The Satb1 protein directs hematopoietic stem cell differentiation toward lymphoid lineages.

Yusuke Satoh, Takafumi Yokota, Takao Sudo, Motonari Kondo, Anne Lai, Paul W Kincade, Taku Kouro, Ryuji Iida, Koichi Kokame, Toshiyuki Miyata and 7 more

Open access · bronzeAbstract read
In one paragraph

Article in Immunity, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed
4.4field-weighted citation impact, top 5% of its field
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

64 citing papers in PubMed, 116 citations in OpenAlex.

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  5. Linker histone regulates the myeloid versus lymphoid bifurcation of multipotent hematopoietic stem and progenitors.Proceedings of the National Academy of Sciences of the United States of America · 2025
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4 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 6 institutions in 2 countries.

Yusuke SatohDepartment of Hematology and Oncology, Osaka University Graduate School of Medicine, Suita, Osaka 565-0871, Japan.
Takafumi Yokota
Takao Sudo
Motonari Kondo
Anne Lai
Paul W Kincade
Taku Kouro
Ryuji Iida
Koichi Kokame
Toshiyuki Miyata
Yoko Habuchi
Keiko Matsui
Hirokazu Tanaka
Itaru Matsumura
Kenji Oritani
Terumi Kohwi-Shigematsu
Yuzuru Kanakura
The University of Osaka · JPDuke Medical Center · USNational Cerebral and Cardiovascular Center · JPOklahoma Medical Research Foundation · USLawrence Berkeley National Laboratory · USNational Institute of Biomedical Innovation, Health and Nutrition · JP

Funding

Studies on gene regulation by chromatin organizationR37CA039681 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI KOHWI-SHIGEMATSU, TERUMI · 2002 to 2015
$9.8M
EARLY EVENTS IN MAMMALIAN B-CELL DIFFERENTIATION.R01AI020069 · NIAID · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI KINCADE, PAUL WAYNE · 1985 to 2012
$5.2M
Hematopoietic Stem Cell SenescenceR01HL107138 · NHLBI · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI ALBEROLA-ILA, JOSE, KINCADE, PAUL WAYNE · 2010 to 2013
$1.6M
EARLY EVENTS IN MAMMALIAN B-CELL DIFFERENTIATIONR37AI020069 · NIAID · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI KINCADE, PAUL WAYNE · 1989 to 1996
–
NCI NIH HHS R37 CA039681NHLBI NIH HHS HL107138-03NHLBI NIH HHS R01 HL107138NIAID NIH HHS AI020069NIAID NIH HHS R01 AI020069
6 · The paper itself

Abstract

How hematopoietic stem cells (HSCs) produce particular lineages is insufficiently understood. We searched for key factors that direct HSC to lymphopoiesis. Comparing gene expression profiles for HSCs and early lymphoid progenitors revealed that Satb1, a global chromatin regulator, was markedly induced with lymphoid lineage specification. HSCs from Satb1-deficient mice were defective in lymphopoietic activity in culture and failed to reconstitute T lymphopoiesis in wild-type recipients. Furthermore, Satb1 transduction of HSCs and embryonic stem cells robustly promoted their differentiation toward lymphocytes. Whereas genes that encode Ikaros, E2A, and Notch1 were unaffected, many genes involved in lineage decisions were regulated by Satb1. Satb1 expression was reduced in aged HSCs with compromised lymphopoietic potential, but forced Satb1 expression partly restored that potential. Thus, Satb1 governs the initiating process central to the replenishing of lymphoid lineages. Such activity in lymphoid cell generation may be of clinical importance and useful to overcome immunosenescence.

Indexed as

LymphopoiesisAnimalsCell DifferentiationCell LineageCells, CulturedCell SurvivalCellular SenescenceChromatin Assembly and DisassemblyGene Expression RegulationHematopoietic Stem CellsHumansMatrix Attachment Region Binding ProteinsMiceMice, Inbred C57BLMice, KnockoutT-LymphocytesMatrix Attachment Region Binding ProteinsSatb1 protein, mouse

Identifiers

PMID23791645
PMCPMC3777575
OpenAlexW2014644369

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

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.