Evidence map›Paper›PMID 22387002›Full record

ArticleDevelopmental cell2012

Trophoblasts regulate the placental hematopoietic niche through PDGF-B signaling.

Akanksha Chhabra, Andrew J Lechner, Masaya Ueno, Asha Acharya, Ben Van Handel, Yanling Wang, M Luisa Iruela-Arispe, Michelle D Tallquist, Hanna K A Mikkola

Open access · bronzeAbstract read
In one paragraph

Article in Developmental cell, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
4.0field-weighted citation impact, top 7% 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

28 citing papers in PubMed, 53 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Murine Placental Erythroid Cells Are Mainly Represented by CD45International journal of molecular sciences · 2023
    Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Hypoxia and Placental Development.Birth defects research · 2017
    Review
  18. Extrinsic regulation of hematopoietic stem cells in development, homeostasis and diseases.Wiley interdisciplinary reviews. Developmental biology · 2017
    Review
  19. Article
  20. 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

9 authors at 2 institutions in 1 country.

Akanksha ChhabraMolecular Biology Institute, University of California, Los Angeles, Los Angeles, CA 90095, USA.
Andrew J Lechner
Masaya Ueno
Asha Acharya
Ben Van Handel
Yanling Wang
M Luisa Iruela-Arispe
Michelle D Tallquist
Hanna K A Mikkola
University of California, Los Angeles · USThe University of Texas Southwestern Medical Center · US

Funding

UCLA NIGMS T32 Program AssessmentT32GM007185 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI TORRES, JORGE · 1985 to 2020
$21.7M
Vascular Biology Training GrantT32HL069766 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI LUSIS, ALDONS JAKE · 2002 to 2022
$7.4M
PDGF Receptor Signaling in Mammalian DevelopmentR01HL074257 · NHLBI · UT SOUTHWESTERN MEDICAL CENTER · PI TALLQUIST, MICHELLE D · 2003 to 2014
$3.7M
PDGF-B signaling in fetal hematopoietic stem cell microenvironmentsR01HL097766 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI MIKKOLA, HANNA KATRI ANNIKKI · 2009 to 2012
$1.5M
Howard Hughes Medical InstituteNHLBI NIH HHS R01 HL074257NHLBI NIH HHS R01 HL097766NHLBI NIH HHS R01 HL097766-01NHLBI NIH HHS T32 HL069766NHLBI NIH HHS T32 HL69766NIGMS NIH HHS GM007185NIGMS NIH HHS T32 GM007185
6 · The paper itself

Abstract

The placenta is a hematopoietic organ that supports hematopoietic stem/progenitor cell (HSPC) generation and expansion without promoting differentiation. We identified PDGF-B signaling in trophoblasts as a key component of the unique placental hematopoietic microenvironment that protects HSPCs from premature differentiation. Loss of PDGF-B or its receptor, PDGFRβ, induced definitive erythropoiesis in placental labyrinth vasculature. This was evidenced by accumulation of CFU-Es and actively proliferating definitive erythroblasts that clustered around central macrophages, highly reminiscent of erythropoiesis in the fetal liver. Ectopic erythropoiesis was not due to a requirement of PDGF-B signaling in hematopoietic cells but rather in placental trophoblasts, which upregulated Epo in the absence of PDGF-B signaling. Furthermore, overexpression of hEPO specifically in the trophoblasts in vivo was sufficient to convert the placenta into an erythropoietic organ. These data provide genetic evidence of a signaling pathway that is required to restrict erythroid differentiation to specific anatomical niches during development.

Indexed as

AnimalsCell DifferentiationErythroid Precursor CellsErythropoiesisErythropoietinFemaleHematopoietic Stem CellsHumansMacrophagesMicePlacentaPregnancyProto-Oncogene Proteins c-sisReceptor, Platelet-Derived Growth Factor betaSignal TransductionTrophoblastsErythropoietinProto-Oncogene Proteins c-sisReceptor, Platelet-Derived Growth Factor beta

Identifiers

PMID22387002
PMCPMC3395466
OpenAlexW1991447499

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.