Evidence map›Paper›PMID 35641778›Full record

ArticleIn vitro cellular & developmental biology. Animal2022

Extramedullary hematopoiesis: mesenchymal stromal cells from spleen provide an in vitro niche for myelopoiesis.

Sawang Petvises, Vinson Tran, Ying-Ying Hey, Dipti Talaulikar, Terence J O'Neill, Jonathan Tan, Helen C O'Neill

Open access · hybridAbstract read
In one paragraph

Article in In vitro cellular & developmental biology. Animal, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.6field-weighted citation impact, top 30% 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

1 citing paper in PubMed, 5 citations in OpenAlex.

  1. 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

7 authors at 3 institutions in 2 countries.

Sawang PetvisesDepartment of Medical Technology, Faculty of Allied Health Sciences, Thammasat University, Bangkok, Thailand.
Vinson TranResearch School of Biology, Australian National University, Canberra, Australia.
Ying-Ying HeyClem Jones Centre for Regenerative Medicine, Faculty of Health Sciences and Medicine, Bond University, Gold Coast, QLD, 4229, Australia.
Dipti TalaulikarANU Medical School, Australian National University, Canberra, Australia.
Terence J O'NeillBond Business School, Bond University, Gold Coast, QLD, Australia.
Jonathan TanClem Jones Centre for Regenerative Medicine, Faculty of Health Sciences and Medicine, Bond University, Gold Coast, QLD, 4229, Australia.
Helen C O'NeillClem Jones Centre for Regenerative Medicine, Faculty of Health Sciences and Medicine, Bond University, Gold Coast, QLD, 4229, Australia. honeill@bond.edu.au.
Bond University · AUAustralian National University · AUThammasat University · TH

Funding

Australian National University Postgraduate scholarshipAustralian Research Council DP13010307Ministry of Science and Technology of Thailand Postgraduate scholarshipNational Health and Medical Research Council 585443National Health and Medical Research Council CJ Martin Fellowship
6 · The paper itself

Abstract

Murine spleen has been shown to harbour stromal cells that support hematopoiesis with production of myeloid antigen-presenting cells. Similar stromal lines have now been isolated from long-term cultures (LTC) of human spleen. When human progenitor populations from spleen, bone marrow and cord blood were employed as a source of progenitors for co-culture above splenic stromal lines, myelopoiesis was supported. Human splenocytes gave production of predominantly myeloid dendritic-like cells, with minor subsets resembling conventional dendritic cells (cDC) cells, and myeloid or monocyte-derived DC. Human bone marrow progenitors gave rise to myelopoiesis from hematopoietic progenitors, while human cord blood supported limited myelopoiesis from existing myeloid precursors. Transcriptome analysis compared two stromal lines differing in myelopoietic support capacity. Gene profiling revealed both stromal lines to reflect perivascular reticular cells with osteogenic characteristics. However, the 5C6 stroma which failed to support hematopoiesis uniquely expressed several inhibitors of the WNT pathway. Combined data now show that splenic stroma of both human and murine origin provides a mesenchymal stromal cell microenvironment which is WNT pathway-dependent, and which supports in vitro myelopoiesis with production of specific subsets of myeloid and dendritic-like cells.

Indexed as

Hematopoiesis, ExtramedullaryMesenchymal Stem CellsAnimalsBone Marrow CellsCells, CulturedHematopoiesisMiceMyelopoiesisSpleenStromal CellsMyelopoiesisNicheSpleenStroma

Identifiers

PMID35641778
PMCPMC9213314
OpenAlexW4281619820

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.