Evidence map›Paper›PMID 24101231›Full record

ReviewCalcified tissue international2014

Cellular complexity of the bone marrow hematopoietic stem cell niche.

Laura M Calvi, Daniel C Link

Abstract readReview
In one paragraph

Review in Calcified tissue international, 2014. 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
–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

28 citing papers in PubMed.

  1. Review
  2. Stem Cell Niche Concept: Search for Current Expert Consensus.International journal of molecular sciences · 2025
    Review
  3. Article
  4. Article
  5. Influences on the Hematopoietic Stem Cell Niche.SciBase hematology & blood disorders · 2024
    Article
  6. Review
  7. Review
  8. Article
  9. Review
  10. Article
  11. Review
  12. Hemmule: A Novel Structure with the Properties of the Stem Cell Niche.International journal of molecular sciences · 2020
    Article
  13. Review
  14. Article
  15. Circadian Regulation in Tissue Regeneration.International journal of molecular sciences · 2019
    Review
  16. Article
  17. Article
  18. Article
  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

2 authors.

Laura M CalviDivision of Endocrinology and Metabolism, Department of Medicine, School of Medicine and Dentistry, University of Rochester, Rochester, NY, USA, laura_calvi@urmc.rochester.edu.
Daniel C Link

Funding

Targeting the Bone Marrow Microenvironment In Acute Lymphocytic LeukemiaP50CA171963 · NCI · WASHINGTON UNIVERSITY · PI Daniel C Link · 2013 to 2026
$31.6M
Universiity of Rochester Center for Medical Countermeasures against RadiationU19AI091036 · NIAID · UNIVERSITY OF ROCHESTER · PI FINKELSTEIN, JACOB N · 2010 to 2014
$15.6M
ROLE OF THE G-CSF RECEPTOR IN PROGENITOR MOBILIZATIONR01HL060772 · NHLBI · WASHINGTON UNIVERSITY · PI LINK, DANIEL C · 1999 to 2014
$3.9M
PGE2 mitigation of acute and late radiation injuryU01AI107276 · NIAID · UNIVERSITY OF ROCHESTER · PI CALVI, LAURA M, PALIS, JAMES · 2013 to 2017
$2.9M
Regulatory Cell Signals in the Bone MarrowR01DK081843 · NIDDK · UNIVERSITY OF ROCHESTER · PI CALVI, LAURA M · 2009 to 2013
$1.8M
Therapeutic Targeting of Leukemia-Microenvironmental InteractionsR01CA166280 · NCI · UNIVERSITY OF ROCHESTER · PI BECKER, MICHAEL W, CALVI, LAURA M · 2013 to 2017
$1.6M
Hematopoietic-Osteoblastic InteractionsR01DK076876 · NIDDK · UNIVERSITY OF ROCHESTER · PI CALVI, LAURA M · 2008 to 2012
$1.5M
Modulation of aged hematopoietic stem cell nichesR01AG046293 · NIA · UNIVERSITY OF ROCHESTER · PI BECKER, MICHAEL W, CALVI, LAURA M · 2013 to 2017
$954k
NCI NIH HHS P50 CA171963NCI NIH HHS R01 CA166280NHLBI NIH HHS HL60772NHLBI NIH HHS R01 HL060772NIAID NIH HHS U01 AI107276NIAID NIH HHS U19 AI091036NIA NIH HHS R01 AG046293NIDDK NIH HHS DK076876NIDDK NIH HHS DK081843NIDDK NIH HHS R01 DK076876NIDDK NIH HHS R01 DK081843
6 · The paper itself

Abstract

The skeleton serves as the principal site for hematopoiesis in adult terrestrial vertebrates. The function of the hematopoietic system is to maintain homeostatic levels of all circulating blood cells, including myeloid cells, lymphoid cells, red blood cells, and platelets. This action requires the daily production of more than 500 billion blood cells. The vast majority of these cells are synthesized in the bone marrow, where they arise from a limited number of hematopoietic stem cells (HSCs) that are multipotent and capable of extensive self-renewal. These attributes of HSCs are best demonstrated by marrow transplantation, where even a single HSC can repopulate the entire hematopoietic system. HSCs are therefore adult stem cells capable of multilineage repopulation, poised between cell fate choices which include quiescence, self-renewal, differentiation, and apoptosis. While HSC fate choices are in part determined by multiple stochastic fluctuations of cell autonomous processes, according to the niche hypothesis, signals from the microenvironment are also likely to determine stem cell fate. While it had long been postulated that signals within the bone marrow could provide regulation of hematopoietic cells, it is only in the past decade that advances in flow cytometry and genetic models have allowed for a deeper understanding of the microenvironmental regulation of HSCs. In this review, we will highlight the cellular regulatory components of the HSC niche.

Indexed as

AnimalsBone and BonesBone MarrowCell DifferentiationCell LineageHematopoietic Stem CellsHumansStem Cell Niche

Identifiers

PMID24101231
PMCPMC3936515

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.