Inflammatory Signaling Regulates Embryonic Hematopoietic Stem and Lymphoid Progenitor Cell Formation

Blood ◽  
2014 ◽  
Vol 124 (21) ◽  
pp. 2902-2902
Author(s):  
Yan Li ◽  
Virginie Esain ◽  
Li Teng ◽  
Jian Xu ◽  
Isaura Frost ◽  
...  

Abstract Hematopoietic stem cells (HSCs) are defined as cells that can self-renew and provide robust, long-term multilineage engraftment of immunocompromised adults. Only one HSC is sufficient to reconstitute the entire hematopoietic system of an adult mouse, thus blood should theoretically be a simple organ system to generate from embryonic stem cells or induced pluripotent stem cells. Yet, despite two decades of effort, no one has been able to produce HSCs ex vivo from these sources. In the vertebrate embryo, transient waves of hematopoietic cells are produced prior to the formation of HSCs. While the role of erythrocyte production is self-evident, the necessity of myeloid production in the midgestation embryo is less clear. HSCs differentiate from hemogenic endothelium, and in mammalian embryos briefly accumulate in the aorta/gonad/mesonephros (AGM) region within intra-aortic hematopoietic clusters, although the vast majority of cluster cells are not functional HSCs. Approximately 20% of cells in hematopoietic clusters express a Ly6a-GFP transgene (Ly6a encodes Sca-1), and all lymphoid progenitors, pre-HSCs, and HSCs at embryonic day (E)11.5 are found within the Ly6a-GFP+ population. Genetic profiling of Ly6a-GFP+ and Ly6a-GFP- hematopoietic cluster cells from the AGM region revealed enrichment in gene ontology (GO) terms associated with innate immunity and inflammatory response in the Ly6a-GFP+ population, suggesting inflammatory signaling may regulate the formation of lymphoid progenitors and HSCs. To identify inflammatory cytokines that may be involved in lymphoid progenitor/HSC formation, we performed explant cultures of E9.5 embryos and added inflammatory factors known to induce Sca-1 expression in the adult mouse. Both type I and type II interferons (IFN-α4 and IFN-γ), and to a lesser extent TNFα, induced Ly6a-GFP expression in hematopoietic cells of explanted embryos. IFN-γ receptor 1 (IFN-γR1) was expressed on >80% of Ly6a-GFP+ hematopoietic cluster cells in the AGM, and Stat1 was phosphorylated in response to the addition of either IFN-γ or IFN-α4 to AGM explant cultures, indicating that embryonic hematopoietic stem and progenitor cells (HSPCs) are wired to respond to interferon stimulation. Mouse embryos deficient for IFN-g, the IFN-gR1, or the IFN-a4 receptor had decreased numbers of progenitors with lymphoid potential in the AGM region, as measured by limiting dilution culture on OP9 stromal cells, and IFN-gR1 deficient embryos had fewer HSCs, as determined by transplantation into adult mice. The role of IFN-γ signaling in HSC production in the AGM is evolutionarily conserved, as morpholino (MO) knockdown of IFN-g and its receptor likewise reduced HSPC numbers in the dorsal aorta and caudal hematopoietic tissue of zebrafish embryos, and the subsequent population of rag2 expressing lymphoid cells in the thymus. ChIP-Seq demonstrated that interferon regulatory factor 2 (IRF2) occupied genes in human fetal liver CD34+ HSPCs, with GO analysis indicating innate immunity and interferon signaling as significantly enriched processes, further demonstrating that interferon signaling is active during vertebrate development. IRF2 is a negative regulator of interferon signaling in the adult, and consistent with this, MO-knockdown of IRF2 in the zebrafish embryo enhanced the production of HSPCs, whereas knockdown of the positive effector IRF1 mimicked the phenotype of IFN-g loss. Myeloid cells have previously been shown to produce IFNs, and primitive F4/80+ macrophages were observed in close proximity to hematopoietic cluster cells in the murine AGM region. To determine if the presence of primitive myeloid cells impacted HSPC formation, macrophage specific as well as pan-myeloid knockdown was employed in zebrafish; macrophage depletion by IRF8-MO significantly reduced runx1 expression in the AGM and HSPC production. Significantly, MO-mediated inhibition of PU.1 function, which depletes the majority of myeloid cells, caused an even more striking loss, suggesting IFN-γ is not the only inflammatory mediator, nor primitive macrophages the only myeloid cells, involved in controlling embryonic HSPC production. Together these data demonstrate that myeloid-mediated inflammatory signaling is active in the developing vertebrate embryo, and in the absence of pathogenic challenge function to regulate the production of lymphoid progenitors and definitive HSCs. Disclosures No relevant conflicts of interest to declare.

Haematologica ◽  
2021 ◽  
Author(s):  
Vikas Madan ◽  
Zeya Cao ◽  
Weoi Woon Teoh ◽  
Pushkar Dakle ◽  
Lin Han ◽  
...  

Recurrent loss-of-function mutations of spliceosome gene, ZRSR2, occur in myelodysplastic syndromes (MDS). Mutation/loss of ZRSR2 in human myeloid cells primarily causes impaired splicing of the U12-type introns. To investigate further the role of this splice factor in splicing and hematopoietic development, we generated mice lacking ZRSR2. Unexpectedly, Zrsr2-deficient mice developed normal hematopoiesis with no abnormalities in myeloid differentiation evident in either young or ≥1-year old knockout mice. Repopulation ability of Zrsr2-deficient hematopoietic stem cells was also unaffected in both competitive and non-competitive reconstitution assays. Myeloid progenitors lacking ZRSR2 exhibited mis-splicing of U12-type introns, however, this phenotype was moderate compared to the ZRSR2- deficient human cells. Our investigations revealed that a closely related homolog, Zrsr1, expressed in the murine hematopoietic cells, but not human, contributes to splicing of U12-type introns. Depletion of Zrsr1 in Zrsr2 KO myeloid cells exacerbated retention of the U12-type introns, thus highlighting a collective role of ZRSR1 and ZRSR2 in murine U12-spliceosome. We also demonstrate that aberrant retention of U12-type introns of MAPK9 and MAPK14 leads to their reduced protein expression. Overall, our findings highlight that both ZRSR1 and ZRSR2 are functional components of the murine U12-spliceosome, and depletion of both proteins is required to model accurately ZRSR2-mutant MDS in mice.


2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Natalia Izotova ◽  
Christine Rivat ◽  
Cristina Baricordi ◽  
Elena Blanco ◽  
Danilo Pellin ◽  
...  

AbstractOur mathematical model of integration site data in clinical gene therapy supported the existence of long-term lymphoid progenitors capable of surviving independently from hematopoietic stem cells. To date, no experimental setting has been available to validate this prediction. We here report evidence of a population of lymphoid progenitors capable of independently maintaining T and NK cell production for 15 years in humans. The gene therapy patients of this study lack vector-positive myeloid/B cells indicating absence of engineered stem cells but retain gene marking in both T and NK. Decades after treatment, we can still detect and analyse transduced naïve T cells whose production is likely maintained by a population of long-term lymphoid progenitors. By tracking insertional clonal markers overtime, we suggest that these progenitors can support both T and NK cell production. Identification of these long-term lymphoid progenitors could be utilised for the development of next generation gene- and cancer-immunotherapies.


2020 ◽  
Vol 11 ◽  
Author(s):  
Courtney B. Johnson ◽  
Jizhou Zhang ◽  
Daniel Lucas

Hematopoiesis in the bone marrow (BM) is the primary source of immune cells. Hematopoiesis is regulated by a diverse cellular microenvironment that supports stepwise differentiation of multipotent stem cells and progenitors into mature blood cells. Blood cell production is not static and the bone marrow has evolved to sense and respond to infection by rapidly generating immune cells that are quickly released into the circulation to replenish those that are consumed in the periphery. Unfortunately, infection also has deleterious effects injuring hematopoietic stem cells (HSC), inefficient hematopoiesis, and remodeling and destruction of the microenvironment. Despite its central role in immunity, the role of the microenvironment in the response to infection has not been systematically investigated. Here we summarize the key experimental evidence demonstrating a critical role of the bone marrow microenvironment in orchestrating the bone marrow response to infection and discuss areas of future research.


Biomolecules ◽  
2021 ◽  
Vol 11 (5) ◽  
pp. 667
Author(s):  
Meera Krishnan ◽  
Sahil Kumar ◽  
Luis Johnson Kangale ◽  
Eric Ghigo ◽  
Prasad Abnave

Adult stem cells (ASCs) are the undifferentiated cells that possess self-renewal and differentiation abilities. They are present in all major organ systems of the body and are uniquely reserved there during development for tissue maintenance during homeostasis, injury, and infection. They do so by promptly modulating the dynamics of proliferation, differentiation, survival, and migration. Any imbalance in these processes may result in regeneration failure or developing cancer. Hence, the dynamics of these various behaviors of ASCs need to always be precisely controlled. Several genetic and epigenetic factors have been demonstrated to be involved in tightly regulating the proliferation, differentiation, and self-renewal of ASCs. Understanding these mechanisms is of great importance, given the role of stem cells in regenerative medicine. Investigations on various animal models have played a significant part in enriching our knowledge and giving In Vivo in-sight into such ASCs regulatory mechanisms. In this review, we have discussed the recent In Vivo studies demonstrating the role of various genetic factors in regulating dynamics of different ASCs viz. intestinal stem cells (ISCs), neural stem cells (NSCs), hematopoietic stem cells (HSCs), and epidermal stem cells (Ep-SCs).


2015 ◽  
Vol 39 (10) ◽  
pp. 1099-1110 ◽  
Author(s):  
Iordanis Pelagiadis ◽  
Eftichia Stiakaki ◽  
Christianna Choulaki ◽  
Maria Kalmanti ◽  
Helen Dimitriou

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