Evidence map›Paper›PMID 32504296›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2021

Interactions of Hematopoietic Stem Cells with Bone Marrow Niche.

Xinghui Zhao, Cuiping Zhang, Xiaojing Cui, Ying Liang

Open access · greenAbstract read
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
6.7field-weighted citation impact, top 4% 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

6 citing papers in PubMed, 13 citations in OpenAlex.

  1. 3DACS biomaterials science & engineering · 2026
    Review
  2. Metabolomics of healthy hematopoietic stem cells and leukemic stem cells.Journal of clinical and translational research · 2025
    Article
  3. Article
  4. Review
  5. In vivo bone marrow microenvironment siRNA delivery using lipid-polymer nanoparticles for multiple myeloma therapy.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  6. 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

4 authors at 1 institution in 1 country.

Xinghui ZhaoDepartment of Toxicology and Cancer Biology, University of Kentucky, Lexington, KY, USA.
Cuiping ZhangDepartment of Toxicology and Cancer Biology, University of Kentucky, Lexington, KY, USA.
Xiaojing CuiDepartment of Toxicology and Cancer Biology, University of Kentucky, Lexington, KY, USA.
Ying LiangDepartment of Toxicology and Cancer Biology, University of Kentucky, Lexington, KY, USA. ying.liang@uky.edu.
University of Kentucky · US

Funding

University of Kentucky Markey Cancer Center Support Grant ECIA SupplementP30CA177558 · NCI · UNIVERSITY OF KENTUCKY · PI Bernard Mark Evers · 2013 to 2026
$38.3M
Latexin function in the maintenance and regeneration of the hematopoietic systemR01HL124015 · NHLBI · UNIVERSITY OF KENTUCKY · PI LIANG, YING · 2016 to 2024
$3.6M
Latexin in human hematopoietic stem cell expansionR21HL140213 · NHLBI · UNIVERSITY OF KENTUCKY · PI LIANG, YING · 2017 to 2018
$230k
NCI NIH HHS P30 CA177558NHLBI NIH HHS R01 HL124015NHLBI NIH HHS R21 HL140213
6 · The paper itself

Abstract

Hematopoietic stem cells (HSCs) are ultimately responsible for the lifelong renewal of all blood cell lineages. In the bone marrow (BM), HSCs reside in specialized microenvironments referred to as the "niche." HSC niche consists of complex components including heterogeneous cell populations, growth factors, and extracellular matrix molecules. The crosstalk between HSCs and their niche is essential to regulate the survival, self-renewal, migration, quiescence, and differentiation of HSCs. The application of mice models with endogenous ablation of specific cell types, advanced imaging technologies, high-throughput single-cell RNA sequencing, and single-cell mass cytometry methods have provided deep insights into communications between HSCs and niche cells. In this chapter, we have focused on three important cell types in the BM niche: mesenchymal stem cells (MSCs), osteoblasts (OBs), and endothelial cells (ECs). In order to address the interaction between HSCs and these three cell populations in BM niche, we have described methodology for (1) collecting total BM from femur and tibia of C57BL/6 mice; (2) analyzing or sorting of MSCs, OBs, and ECs based on the selection of surface markers CD45, Ter119, CD31, Sca1, and CD51 with flow cytometry; and (3) co-culturing the sorted cells with purified HSCs for further functional assays of HSCs.

Indexed as

Stem Cell NicheAnimalsBone Marrow CellsHematopoietic Stem CellsMiceMice, Inbred C57BLEndothelial cells (ECs)Hematopoietic stem cells (HSCs)Mesenchymal stem cells/mesenchymal stromal cells (MSCs)Osteoblasts (OBs)

Identifiers

PMID32504296
PMCPMC9423787
OpenAlexW3032951930

What OpenQuestion holds

Textmetadata
LicenceTDM
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.