Please use this identifier to cite or link to this item: https://doi.org/10.1371/journal.pone.0205583
DC FieldValue
dc.titleIdentification of genes which regulate stromadependent in vitro hematopoiesis
dc.contributor.authorPeriasamy P.
dc.contributor.authorTran V.
dc.contributor.authorO'Neill H.C.
dc.date.accessioned2019-11-01T08:12:02Z
dc.date.available2019-11-01T08:12:02Z
dc.date.issued2018
dc.identifier.citationPeriasamy P., Tran V., O'Neill H.C. (2018). Identification of genes which regulate stromadependent in vitro hematopoiesis. PLoS ONE 13 (10) : e0205583. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pone.0205583
dc.identifier.issn19326203
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/161212
dc.description.abstractCultured splenic stroma has been shown to support in vitro hematopoiesis in overlaid bone marrow and spleen progenitors. These co-cultures support longterm production of a novel dendritic-like cell type along with transient production of myeloid cells. They also maintain a progenitor cell population. The splenic stromal lines 5G3 and 3B5 have been identified as a supporter and a non-supporter of hematopoiesis. Based on their gene expression profile, both 5G3 and 3B5 express genes related to hematopoiesis, while 5G3 cells express several unique genes, and show upregulation of some genes over 3B5. Based on gene expression studies, specific inhibitors were tested for capacity to inhibit hematopoiesis in co-cultures. Addition of specific antibodies and small molecule inhibitors identified VCAM1, CXCL12, CSF1 and SPP1 as potential regulators of hematopoiesis, although both are expressed by 5G3 and 3B5. Through inhibition of function, SVEP1 and ALDH1 are also shown here to be deterministic of 5G3 hematopoietic support capacity, since these are uniquely expressed by 5G3 and not 3B5. The achievement of inhibition is notable given the dynamic, longterm nature of co-cultures which involve only small numbers of cells. The alternate plan, to add recombinant soluble factors produced by 5G3 back into 3B5 co-cultures in order to recover in vitro hematopoiesis, proved ineffective. Out of 6 different factors added to 3B5, only IGF2 showed any effect on cell production. The identification of differentially expressed or upregulated genes in 5G3 has provided an insight into potential pathways involved in in vitro hematopoiesis leading to production of dendritic-like cells. © 2018 Periasamy et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20191101
dc.subjectgrowth factor
dc.subjectosteopontin
dc.subjectstromal cell derived factor 1
dc.subjecttranscriptome
dc.subjectvascular cell adhesion molecule 1
dc.subjectrecombinant protein
dc.subjectsignal peptide
dc.subjecttranscriptome
dc.subjectALDH1 gene
dc.subjectanimal cell
dc.subjectArticle
dc.subjectcell count
dc.subjectcell function
dc.subjectcoculture
dc.subjectcontrolled study
dc.subjectCSF1 gene
dc.subjectCXCL12 gene
dc.subjectdendritic cell
dc.subjectgene
dc.subjectgene control
dc.subjectgene expression profiling
dc.subjectgene expression regulation
dc.subjectgene product
dc.subjectgenetic identification
dc.subjecthematopoiesis
dc.subjecthematopoietic stem cell
dc.subjectIGF2 gene
dc.subjectin vitro study
dc.subjectmouse
dc.subjectnonhuman
dc.subjectsignal transduction
dc.subjectSPP1 gene
dc.subjectstroma
dc.subjectstromal cell line
dc.subjectstromal cell line 3B5
dc.subjectstromal cell line 5G3
dc.subjectSVEP1 gene
dc.subjectupregulation
dc.subjectVCAM1 gene
dc.subjectanimal
dc.subjectbone marrow cell
dc.subjectC57BL mouse
dc.subjectcell line
dc.subjectcytology
dc.subjectgene expression
dc.subjectgenetics
dc.subjectgermfree animal
dc.subjecthematopoiesis
dc.subjectmetabolism
dc.subjectphysiology
dc.subjectspleen
dc.subjectstroma cell
dc.subjectAnimals
dc.subjectBone Marrow Cells
dc.subjectCell Line
dc.subjectCoculture Techniques
dc.subjectGene Expression
dc.subjectHematopoiesis
dc.subjectIntercellular Signaling Peptides and Proteins
dc.subjectMice, Inbred C57BL
dc.subjectRecombinant Proteins
dc.subjectSpecific Pathogen-Free Organisms
dc.subjectSpleen
dc.subjectStromal Cells
dc.subjectTranscriptome
dc.typeArticle
dc.contributor.departmentMICROBIOLOGY AND IMMUNOLOGY
dc.description.doi10.1371/journal.pone.0205583
dc.description.sourcetitlePLoS ONE
dc.description.volume13
dc.description.issue10
dc.description.pagee0205583
Appears in Collections:Staff Publications
Elements

Show simple item record
Files in This Item:
File Description SizeFormatAccess SettingsVersion 
10_1371_journal_pone_0205583.pdf2.34 MBAdobe PDF

OPEN

NoneView/Download

Google ScholarTM

Check

Altmetric


This item is licensed under a Creative Commons License Creative Commons