Please use this identifier to cite or link to this item: https://doi.org/10.1371/journal.pone.0205583
Title: Identification of genes which regulate stromadependent in vitro hematopoiesis
Authors: Periasamy P. 
Tran V.
O'Neill H.C.
Keywords: growth factor
osteopontin
stromal cell derived factor 1
transcriptome
vascular cell adhesion molecule 1
recombinant protein
signal peptide
transcriptome
ALDH1 gene
animal cell
Article
cell count
cell function
coculture
controlled study
CSF1 gene
CXCL12 gene
dendritic cell
gene
gene control
gene expression profiling
gene expression regulation
gene product
genetic identification
hematopoiesis
hematopoietic stem cell
IGF2 gene
in vitro study
mouse
nonhuman
signal transduction
SPP1 gene
stroma
stromal cell line
stromal cell line 3B5
stromal cell line 5G3
SVEP1 gene
upregulation
VCAM1 gene
animal
bone marrow cell
C57BL mouse
cell line
cytology
gene expression
genetics
germfree animal
hematopoiesis
metabolism
physiology
spleen
stroma cell
Animals
Bone Marrow Cells
Cell Line
Coculture Techniques
Gene Expression
Hematopoiesis
Intercellular Signaling Peptides and Proteins
Mice, Inbred C57BL
Recombinant Proteins
Specific Pathogen-Free Organisms
Spleen
Stromal Cells
Transcriptome
Issue Date: 2018
Citation: Periasamy 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
Rights: Attribution 4.0 International
Abstract: Cultured 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.
Source Title: PLoS ONE
URI: https://scholarbank.nus.edu.sg/handle/10635/161212
ISSN: 19326203
DOI: 10.1371/journal.pone.0205583
Rights: Attribution 4.0 International
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