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Volume 11 (2011), Article ID 598097, 11 pages
Embryonic Regulation of the Mouse Hematopoietic Niche
1Division of Hematopoietic Stem Cells, Advanced Medical Initiatives, Department of Advanced Medical Initiatives, Faculty of Medical Sciences, Kyushu University, Fukuoka 812-8582, Japan
2Department of Medicine and Biosystemic Science, Graduate School of Medical Sciences, Kyushu University, Fukuoka 812-8582, Japan
3Discipline of Physiology, School of Medical Sciences, University of Sydney, Camperdown, NSW 2050, Australia
Received 16 July 2011; Accepted 16 September 2011
Academic Editor: David Tannahill
Copyright © 2011 Daisuke Sugiyama et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Hematopoietic stem cells (HSCs) can differentiate into several types of hematopoietic cells (HCs) (such as erythrocytes, megakaryocytes, lymphocytes, neutrophils, or macrophages) and also undergo self-renewal to sustain hematopoiesis throughout an organism's lifetime. HSCs are currently used clinically as transplantation therapy in regenerative medicine and are typically obtained from healthy donors or cord blood. However, problems remain in HSC transplantation, such as shortage of cells, donor risks, rejection, and graft-versus-host disease (GVHD). Thus, increased understanding of HSC regulation should enable us to improve HSC therapy and develop novel regenerative medicine techniques. HSC regulation is governed by two types of activity: intrinsic regulation, programmed primarily by cell autonomous gene expression, and extrinsic factors, which originate from so-called “niche cells” surrounding HSCs. Here, we focus on the latter and discuss HSC regulation with special emphasis on the role played by niche cells.
After gastrulation, three germ layers emerge: endoderm, mesoderm, and ectoderm. Among them, mesoderm is the ancestor of hematopoietic cells (HCs), and both extraembryonic and intraembryonic mesoderm contribute to HC generation. In the mouse, the site of blood cell production changes as embryos develop over an approximately 20-day gestation period (Figure 1(a)). Hematopoiesis begins in the yolk sac (YS), producing mainly primitive erythroid cells at 7.5 days postcoitum (dpc). Shortly thereafter, definitive myelo-erythroid progenitor cells appear in the YS (around 8.25 dpc), which then seed the fetal liver (FL). This process, termed primitive hematopoiesis, diminishes at 12.5 dpc, when definitive hematopoiesis, which sustains the adult blood system through HSCs, begins in the FL. Although there is controversy over where HSCs are generated—in the extraembryonic mesoderm at the YS or in the intraembryonic para-aortic-splanchnopleural mesoderm (P-Sp)/aorta-gonad-mesonephros (AGM) region—recent studies suggest that both regions contain HSCs capable of reconstituting adult bone marrow hematopoiesis (Figures 1(a) and 1(b)). In addition, HSCs are generated in the placenta (PL), likely independent of the YS and P-Sp/AGM regions. Thereafter, these HSCs are thought to circulate and colonize the FL, where HSC expansion occurs. HSCs then temporarily reside in fetal spleen and finally shift to fetal bone marrow (BM)  (Figures 1(a) and 1(b)).
2. THE YOLK SAC
The YS is a bilaminar membranous sac encasing the embryo proper. It is here the “blood islands,” the first site of hematopoiesis. The YS is composed of two distinct layers of cells, the visceral endoderm which is predominantly an absorptive epithelium transporting nutrients to the embryo and the extraembryonic mesoderm which gives rise to the endothelium of the YS and the blood cells that fill these early vessels . Developing mesoderm cells can be programmed either by the visceral endoderm or by soluble factors produced by the visceral endoderm such as Indian hedgehog (Ihh) to become hematopoietic or vascular cells [3, 4] (Figure 2). The extraembryonic mesoderm gives rise to the first hematopoietic cells in the developing conceptus. These include the primitive erythroid cells, macrophages, and megakaryocytes and appear shortly after gastrulation . The primitive erythroid (EryP) cells are larger than their adult-type definitive counterparts (EryD) and express a unique set of embryonic globin genes . EryP dominate the mid-gestation circulation of the mouse embryo and number in the several millions; however, by birth, they will be greatly reduced in frequency, diluted by the vast numbers of EryD generated in the FL [7, 8].
The niche supporting early hematopoietic development in the YS is poorly defined. However, recently some players in this field have been identified. YS endothelial cells and the visceral endoderm express the soluble growth factor angiopoietin 1, whereas early EryP cells express the angiopoietin receptor Tie-2. Interestingly, the EryP cells themselves express soluble growth factors . TGFb1 expression was detected in the visceral endoderm and the EryP, suggesting that the developing hematopoietic cells may be generating a unique niche themselves. The hypoxic nature of the developing YS is also supportive of hematopoiesis [9, 10]. As the YS develops, a broad range of hematopoietic progenitors are generated. These include definitive erythroid progenitors, myeloid progenitors, and lymphoid progenitors [5, 11, 12]. The migration of hematopoietic progenitors throughout the developing embryo has been investigated capitalizing on knockout mouse strains lacking a heartbeat and subsequent blood flow. These mice lacked the sodium/calcium exchanger Ncx1, failed to develop a heartbeat, and subsequently hematopoietic progenitors remained lodged at their sites of origin, namely, the YS  and the placenta . Whether the progenitors isolated in the Ncx-1 knockout placenta are truly HSC is yet to be resolved . Shortly before mid-gestation in the mouse embryo, long-term reconstituting HSCs appear in the YS . These cells show significant differences compared to the HSCs generated within the embryo; however, they are capable of giving rise to the hematopoietic system of newborn mice [15, 16]. The origin of HSC has proven a contentious issue; however, the development of genetic models to monitor HSC sites of production has supported the YS as, at least one, source of HSC during embryogenesis. Genetic “tagging and tracing” of early hematopoietic progenitors expressing the transcriptional regulator Runx1 in the YS suggests that this may indeed be a site of HSC production during embryogenesis .
3. THE AGM REGION
After YS hematopoiesis, HSC activity is detected in the p-Sp/AGM region, where cell aggregates, termed HC clusters or intra-aortic/arterial clusters (IACs), are observed. HSCs in the AGM region express c-Kit/CD117 (the receptor for stem cell factor), CD31/PECAM-1 (platelet/endothelial cell adhesion molecule 1), and CD34 (a transmembrane glycoprotein). Presumptive pre-HSCs expressing c-Kit and capable of reconstituting neonatal recipients are detected in the p-Sp/AGM region at 9.5 dpc, whereas functional c-Kit-expressing HSCs capable of reconstituting adult recipients are first identified in the AGM region at 10.5 dpc. Special microenvironments likely enable pre-HSCs from the p-Sp/AGM region at 9.5 dpc to acquire functional HSC activity by 10.5 dpc. In the AGM region, IACs are frequently observed attached to floors and walls of large arteries, suggesting that they are generated from EC layers (Figure 3(a)). Mouse IACs have been characterized morphologically and are primarily located in the dorsal aorta, the omphalomesenteric artery, and the umbilical artery. Intrinsic regulation of AGM HSCs has been well characterized. The transmembrane receptor encoded by Notch1 is essential to generate HSCs from ECs , and the ubiquitin ligase Mind bomb-1 (encoded by Mib1), which regulates Notch ligands, is important for intraembryonic hematopoiesis not only in aortic ECs but in subaortic patches . Runx1 appears to be required for formation of intra-aortic HC clusters from ECs . Several reports suggest that extrinsic regulation of AGM HSCs is also important. Thrombopoietin (TPO)/Mpl (TPO receptor) signaling plays a role in transition from hemogenic ECs to hematopoietic progenitor cells (HPCs)/HSCs via Runx1 activation and in production of HPCs/HSCs via Meis1 and Homeobox (Hox) b4 activation from 10.0 dpc to 10.5 dpc in AGM region . Intereukin-1 (IL-1) reportedly functions as an important homeostatic regulator at earliest stages of HSC development, limiting differentiation of some HSCs along the myeloid lineage  (Figure 3(b)). However, it remains unclear which factors regulate AGM HSCs. Since the AGM region consists of ECs, gonad cells, mesonephros cells, and unclassified MCs, those cells likely comprise a niche for HSC generation. c-Kit−/CD34− MCs of the AGM region reportedly express hedgehog receptor/transducer genes, namely, Ptch1, Ptch2, and Smo, as well as genes encoding their downstream effectors, Gli1, Gli2, and Gli3, which act to increase the number of HSCs at 10.5 dpc. In addition, ECs (CD31+/CD34+/Kit-) of the AGM region at 10.5 dpc likely function in HSC regulation through stem cell factor (SCF) secretion . Taken together, the niche is comprised of several factors governing HSC generation.
4. THE PLACENTA
The PL is a highly vascularized structure that functions not only in gas exchange and fetal nutrition but in hematopoiesis at 8.5–13.5 dpc . Similar to the AGM region, c-Kit-positive HC clusters in the PL are observed in the vitelline and umbilical arteries of the placenta (Figure 4(a)). A significant proportion of HPCs, including highly proliferative potential colony forming cells (HPP-CFCs), are detected in the mouse placenta . HSCs (c-Kit+/CD34+) by 11.5 dpc, and the number increase until 12.5 dpc, resulting in a 15-fold increase in HSC activity compared with that of the AGM region [26, 27]. These findings indicate that mouse PL is a likely site for HSC generation and expansion at mid-gestation. Formation of HC clusters in both the AGM region and PL is impaired in mutant mice deficient in genes encoding specific transcription factors, namely, Runx1, Evi-1, and c-Myb, suggesting the importance of intrinsic regulation [7, 20, 28, 29]. Relevant to extrinsic regulation of PL HSCs, IL-3 not only is a target of Runx1 in adult HCs, but also regulates HSC proliferation in the PL . We previously demonstrated regulation of HC clusters in the PL by surrounding niche cells . To do so, we used laser-capture microdissection and flow cytometry to capture niche cells. Among several cytokine genes, only SCF was expressed in niche cells, particularly in ECs. SCF protein expression was confirmed by ELISA and immunohistochemistry. Administration of blocking antibodies to c-Kit, the SCF receptor, clearly demonstrated that SCF/c-Kit signaling is pivotal for HSC regulation in the PL  (Figure 4(b)). Based on gene expression analysis, niche cells do not express IL-3 , although future studies are required to clarify its function in vivo.
5. FETAL LIVER
Hematopoiesis occurs in fetal liver (FL) by mid-gestation [31–33]. After HSCs are generated in the YS, AGM region, and PL, they migrate into FL, where HSCs are maintained and the number of HSCs dramatically increases between 12 and 16 dpc, during which time differentiation of mature HCs, particularly erythrocytes, occurs [32–34]. Thus FL is an organ appropriate for investigation of HSC expansion and erythropoiesis in vitro. FL HSCs express the markers c-Kit, stem cell antigen-1 (Sca-1), and protein tyrosine phosphatase, receptor type, C (CD45, also known as common leukocyte antigen). Circulating HPCs and HSCs expressing c-Kit have been reported to colonize FL . Both morphological observation and experiments in vitro suggest that FL itself does not produce HSCs or HPCs but may be colonized by HCs of extrinsic origin after 9.5 dpc [32, 33, 36, 37]. Intrinsic regulation of hematopoiesis in FL has also been reported. Factors that function in that activity include PU.1, an ETS family transcription factor, which functions in maintenance (differentiation) or expansion of FL HSCs . Class I Hoxb4 and Hoxb3 also positively regulate HSC and HPC proliferation by accelerating the cell cycle . Cited2 (a CBP/p300-interacting transactivator with a glutamic acid [E] and aspartic acid [D]-rich tail 2) maintains FL HSCs and HPCs . Relevant to extrinsic regulation of FL hematopoiesis, FL consists of hepatoblasts (hepatocyte precursors), ECs, hematopoietic cells [41, 42], and other cells such as MCs (Figure 5(a)). Among them, we recently demonstrated that hepatoblasts expressing Dlk-1 function in HSC differentiation, particularly erythropoiesis, through secretion of erythropoietin (EPO), a cytokine regulating erythroid differentiation and SCF  (Figure 5(b)). In addition, hepatoblasts (SCF+DLK+) function at 15.5 dpc in FL to increase the number of HSCs likely through production of several cytokines, angiopoietin-like 3 (Angptl3), insulin-like growth factor-2 (IGF2), SCF, and thrombopoietin (TPO) . Taken together, hepatoblasts comprise a niche for HSC regulation through cytokine secretion. However, it remains unclear how HSCs maintain self-renewal capacity under intense exposure to cytokines, which stimulate HSC differentiation. Also, in addition to cytokines, the extracellular matrix (ECM), including the interstitial matrix and basement membrane, interacts with cell surface receptors to regulate hematopoiesis extrinsically in FL. Integrins, which function as receptors for ECM, are important effectors of cell adhesion, differentiation, and migration. Particularly in FL hematopoiesis, beta-1 integrin (fibronectin receptor, CD29) is reportedly crucial for HSC colonization [45–48]. Interaction of integrin heterodimers with ECMs could function as a homing mechanism and enable HSCs and hematopoietic progenitor cells (HPCs) to reside in FL [49–51]. ECM proteins are produced in various cell types and interact with cytokines, enabling cells to interpret cytokine signaling in a particular context .
6. FETAL SPLEEN AND BONE MARROW
After the number of HSCs increases in the FL, those cells home to fetal-spleen, where HSCs differentiate at 13.5 to 14.5 dpc . Fetal spleen-derived stromal cells enable HSCs to differentiate primarily into macrophages (F4/80+Mac1+) rather than lymphocytes. After transient hematopoiesis in fetal spleen, HSCs gradually home to BM after 16.5 dpc, where they remain during their entire lifetime. Although fetal BM is formed by 15.5 dpc, HSCs capable of self-renewal and which are positive for the signaling lymphocyte activation molecule (SLAM) family marker CD150 and negative for CD48 and CD41 cannot be detected in this tissue until 17.5 dpc, suggesting that other mechanisms govern the ability of HSCs to home to fetal BM during this period. Expression of genes encoding HSC migration factors, such as Cxcr4 (a chemokine receptor), Col4a1 (related to type IV collagen alpha1 synthesis), Mmp2, Timp2 (related to degradation and regulation of development), is significantly upregulated in HSCs during embryonic development .
7. CONCLUDING REMARKS
During embryogenesis, extrinsic regulation by niche cells is pivotal for HSC generation, expansion, differentiation, and maintenance. Increased knowledge of niche cell regulation should facilitate development of novel methods of in vitro generation, expansion, and differentiation for HSCs. Furthermore, if artificial niche components that replicate internal environment in vivo could maintain the status of stem cell, for example, cell cycle and quiescence, migration of both normal HSCs and leukemic stem cells might be directed as planned. The study of niche regulation of hematopoiesis should impact novel stem cell engineering, which could be applied for clinical therapies in the future.
|dpc:||Days post coitum|
|HSC:||Hematopoietic stem cell|
|HPC:||Hematopoietic progenitor cell|
The authors acknowledge grant support from Health and Labour Sciences Research Grant from Ministry of Health, Labour and Welfare, and the Tokyo Biochemical Research Foundation. Dr. T. Inoue is supported by a research fellowship from the Japan Society for the Promotion of Science. Dr. K. Kulkeaw is supported by a research fellowship from the Tokyo Biochemical Research Foundation. The autors thank Dr. K. Akashi, Dr. K. Tani, Ms. S. Okayama and Dr. K. Srinoun for helpful discussion, and Dr. Elise Lamar for critical reading of the paper.
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