RESUMEN
The adenomatous polyposis coli gene (APC) is mutated in familial adenomatous polyposis and in sporadic colorectal tumors. Here the APC gene product is shown to bind through its armadillo repeat domain to a Rac-specific guanine nucleotide exchange factor (GEF), termed Asef. Endogenous APC colocalized with Asef in mouse colon epithelial cells and neuronal cells. Furthermore, APC enhanced the GEF activity of Asef and stimulated Asef-mediated cell flattening, membrane ruffling, and lamellipodia formation in MDCK cells. These results suggest that the APC-Asef complex may regulate the actin cytoskeletal network, cell morphology and migration, and neuronal function.
Asunto(s)
Proteínas del Citoesqueleto/metabolismo , Factores de Intercambio de Guanina Nucleótido/metabolismo , Transactivadores , Proteínas de Unión al GTP rac/metabolismo , Proteína de la Poliposis Adenomatosa del Colon , Secuencia de Aminoácidos , Animales , Encéfalo/metabolismo , Línea Celular , Membrana Celular/ultraestructura , Tamaño de la Célula , Colon/citología , Colon/metabolismo , Citoplasma/metabolismo , Factores de Intercambio de Guanina Nucleótido/química , Factores de Intercambio de Guanina Nucleótido/genética , Guanosina Difosfato/metabolismo , Humanos , Immunoblotting , Mucosa Intestinal/citología , Mucosa Intestinal/metabolismo , Ratones , Datos de Secuencia Molecular , Neuronas/metabolismo , Pruebas de Precipitina , Unión Proteica , Estructura Terciaria de Proteína , Ratas , Proteínas Recombinantes de Fusión/metabolismo , Factores de Intercambio de Guanina Nucleótido Rho , Transducción de Señal , Transfección , Técnicas del Sistema de Dos Híbridos , beta CateninaRESUMEN
To investigate the mechanisms of peroxisome assembly and the molecular basis of peroxisome assembly disorders, we isolated and characterized a peroxisome-deficient CHO cell mutant, ZP139, which was found to belong to human complementation group II, the same group as that of our earlier mutant, ZP105. These mutants had a phenotypic deficiency in the import of peroxisomal targeting signal type 1 (PTS1) proteins. Amino-terminal extension signal (PTS2)-mediated transport, including that of 3-ketoacyl coenzyme A thiolase, was also defective in ZP105 but not in ZP139. PEX5 cDNA, encoding the PTS1 receptor (PTS1R), was isolated from wild-type CHO-K1 cells. PTS1R's deduced primary sequence comprised 595 amino acids, 7 amino acids less than the human homolog, and contained seven tetratricopeptide repeat (TPR) motifs at the C-terminal region. Chinese hamster PTS1R showed 94, 28, and 24% amino acid identity with PTS1Rs from humans, Pichia pastoris, and Saccharomyces cerevisiae, respectively. A PTS1R isoform (PTS1RL) with 632 amino acid residues was identified in CHO cells; for PTS1R, 37 amino acids were inserted between residues at positions 215 and 216 of a shorter isoform (PTS1RS). Southern blot analysis of CHO cell genomic DNA suggested that these two isoforms are derived from a single gene. Both types of PEX5 complemented impaired import of PTS1 in mutants ZP105 and ZP139. PTS2 import in ZP105 was rescued only by PTS1RL. This finding strongly suggests that PTS1RL is also involved in the transport of PTS2. Mutations in PEX5 were determined by reverse transcription-PCR: a G-to-A transition resulted in one amino acid substitution: Gly298Glu of PTS1RS (G335E of PTS1RL) in ZP105 and Gly485Glu of PTS1RS (G522E of PTS1RL) in ZP139. Both mutations were in the TPR domains (TPR1 and TPR6), suggesting the functional consequence of these domains in protein translocation. The implications of these mutations are discussed.
Asunto(s)
Microcuerpos/genética , Receptores Citoplasmáticos y Nucleares/genética , Secuencia de Aminoácidos , Animales , Células CHO , Cricetinae , Proteínas Fúngicas , Regulación de la Expresión Génica , Humanos , Microcuerpos/metabolismo , Datos de Secuencia Molecular , Mutación , Receptor de la Señal 2 de Direccionamiento al Peroxisoma , Receptor de la Señal 1 de Direccionamiento al Peroxisoma , Alineación de SecuenciaRESUMEN
LIM-kinase 1 and 2 (LIMK1 and LIMK2) are members of a novel class of protein kinases with structures composed of two LIM motifs at the N-terminus and an unusual protein kinase domain at the C-terminus. The cellular functions of the LIMK family proteins have remained unknown. In the present study, we examined effects of LIMKs on neuronal differentiation of PC12 pheochromocytoma cells. Transient expression analyses revealed that LIMK1, in itself, had no apparent effect on PC12 cells, but the oncogenic Ras-induced differentiation of PC12 cells was notably inhibited by co-expression with LIMK1 or LIMK2. A mutant of LIMK1 lacking a protein kinase domain (delta K) similarly inhibited Ras-induced differentiation of PC12 cells, but a mutant lacking a LIM domain (delta LIM) failed to do so, indicating that a LIM domain but not a protein kinase domain is required for the inhibitory activity. This notion was further supported by the finding that mutation, changing conserved cysteines involved in zinc coordination to glycines in both of two LIM motifs, abolished the inhibitory activity of delta K. Additionally, we also found that the constitutively activated MAP kinase kinase (MAPKK)-induced differentiation of PC12 cells was inhibited by co-expression with delta K. Furthermore, AK did not inhibit the kinase activity of MAP kinase (MAPK) stimulated by MAPKK, when co-expressed in COS7 cells. These findings suggest that LIMK1 inhibits neuronal differentiation of PC12 cells, through its LIM domain and by interfering with events downstream of MAPK activation.
Asunto(s)
Isoenzimas/metabolismo , Neuronas/citología , Neuronas/fisiología , Proteínas Quinasas/metabolismo , Proteínas ras/fisiología , Animales , Sitios de Unión , Diferenciación Celular/fisiología , Activación Enzimática , Regulación Enzimológica de la Expresión Génica , Humanos , Isoenzimas/genética , Quinasas Lim , Quinasas de Proteína Quinasa Activadas por Mitógenos , Mutación , Neuronas/enzimología , Células PC12 , Proteínas Quinasas/genética , Estructura Terciaria de Proteína , Ratas , Transfección , Proteínas ras/genéticaRESUMEN
1,25-dihydroxyvitamin D3 (1,25(OH)2D3) is thought to be an important systemic factor in the fracture repair process, but the mechanism of action of 1,25(OH)2D3 has not been clearly defined. In this study, the role of 1,25(OH)2D3 in the fracture repair process was analyzed in a rat closed femoral fracture model. The plasma concentration of 1,25(OH)2D3 rapidly decreased on day 3 and continued to decrease to 10 days after fracture. We assessed whether this decrease was based on the accelerated degradation or retardation of the synthesis rate of 1,25(OH)2D3, from 25(OH)D3. After radiolabeled 3H-1,25(OH)2D3 or 3H-25(OH)D3 was injected i.v. into fractured or control (unfractured) rats, the concentrations of 25(OH)D3 and 1,25(OH)2D3 metabolites were measured by HPLC. The plasma concentrations of these radiolabeled metabolites in fractured group were similar to those in control rats early after operation. However, radioactivity in the femurs of fractured rats was higher than that of the control group. Furthermore, the radioactivity was concentrated in the callus of the fractured group analyzed by autoradiography. 1,25(OH)2D3 receptor gene expression was detected early after fracture and, additionally, both in the soft and hard callus on days 7 and 13 after fracture. These results showed that the rapid disappearance of 1,25(OH)2D3 in the early stages after fracture was not due to either increased degradation or decreased synthesis of 1,25(OH)2D3, but rather to increased consumption. Further, these results suggest the possibility that plasma 1,25(OH)2D3 becomes localized in the callus and may regulate cellular events in the process of fracture healing.
Asunto(s)
Calcitriol/sangre , Calcitriol/metabolismo , Fracturas del Fémur/metabolismo , Curación de Fractura/fisiología , Animales , Autorradiografía , Calcifediol/sangre , Calcifediol/metabolismo , Cartílago/química , Cartílago/metabolismo , Cromatografía Líquida de Alta Presión , Femenino , Fémur/química , Fémur/metabolismo , Cinética , ARN Mensajero/análisis , Ratas , Ratas Sprague-Dawley , Receptores de Calcitriol/genética , TritioRESUMEN
By transfection of the expression plasmid containing a human c-met cDNA into COS-7 cells, high-affinity binding sites specific for HGF with a Kd value of 30 pM were newly detected. Furthermore, only in the c-met transfected COS-7 cells, but not in the control COS-7 cells, DNA synthesis was markedly induced in response to HGF. Thus, transient expression of exogenous c-met cDNA resulted in the appearance of high-affinity receptor for HGF and conversion of the normally non-responsive COS-7 cells into the HGF-responsive cells. These results provide evidence for identifying the c-met product as a signal transducing high-affinity receptor for HGF.
Asunto(s)
Expresión Génica , Proteínas Tirosina Quinasas/genética , Proteínas Proto-Oncogénicas/genética , Receptores de Superficie Celular/genética , Transducción de Señal , Línea Celular , ADN/genética , Humanos , Radioisótopos de Yodo , Mitógenos , Plásmidos , Reacción en Cadena de la Polimerasa , Proto-Oncogenes Mas , Proteínas Proto-Oncogénicas c-met , Uridina/metabolismoRESUMEN
LIM-kinase 1 (LIMK1) and 2 (LIMK2) are members of a novel class of protein kinases containing two LIM motifs at the N-terminus. The LIM motif is thought to be involved in protein-protein interactions. We report here evidence that LIMK1 self-associates and also associates with LIMK2. In vivo and in vitro binding analyses using variously deleted mutants of LIMKI revealed that the self-association of LIMK1 was caused by interaction between the N-terminal LIM domain and the C-terminal kinase domain. The association of LIMK1 with itself and with LIMK2 is important for understanding how activities and functions of LIMK family kinases are regulated.
Asunto(s)
Proteínas de Unión al ADN/metabolismo , Proteínas Quinasas/metabolismo , Animales , Secuencia de Bases , Células COS , Cartilla de ADN , Proteínas de Unión al ADN/química , Quinasas Lim , Datos de Secuencia Molecular , Unión Proteica , Proteínas Serina-Treonina QuinasasRESUMEN
LIM-kinase 1 (LIMK1) is a serine/threonine kinase containing two LIM motifs at the N-terminus. The functional role of LIMK1 has remained unknown. In this study, we examined the role of LIMK1 in cell growth of fibroblasts. Induced expression of LIMK1 in NIH3T3 cells led to growth retardation. Transfection of LIMK1 sense cDNA into NIH3T3 and H-ras-transformed FYJ10 fibroblasts significantly suppressed colony formation of these cells. In contrast, transfection with LIMK1 antisense cDNA strongly stimulated colony formation of the NIH3T3 cells. These findings suggest that LIMK1 functions as a negative regulator of fibroblast cell growth, and may play a role in tumor suppression.
Asunto(s)
Proteínas de Unión al ADN/biosíntesis , Fibroblastos/citología , Proteínas Serina-Treonina Quinasas/biosíntesis , Células 3T3/metabolismo , Animales , División Celular/genética , Línea Celular Transformada , Células Cultivadas , Ensayo de Unidades Formadoras de Colonias , ADN Complementario , Proteínas de Unión al ADN/genética , Fibroblastos/metabolismo , Genes ras , Quinasas Lim , Ratones , Microinyecciones , Proteínas Quinasas , Proteínas Serina-Treonina Quinasas/genética , Ratas , TransfecciónRESUMEN
Using 125I-labeled hepatocyte growth factor (HGF) as a ligand, we examined the tissue distribution of the HGF receptor in adult rats. Specific binding of 125I-HGF was detected in the plasma membranes of liver, spleen, kidney, lung, adrenal gland, pituitary, and thyroid. Scatchard analysis of HGF binding in liver, spleen, kidney, lung, and adrenal gland revealed the presence of a single class of high affinity receptor with a dissociation constant (Kd) of 20-30 pM. The maximum number of binding sites (Bmax) was determined to be 400-3,000 sites per ng of plasma membrane protein, the highest number being in the liver. Such a wide distribution of a high affinity HGF receptor indicates that HGF may be a multifunctional growth factor, targeting to a variety of organs, and not restricted to liver. After 70% partial hepatectomy, specific binding of 125I-HGF to membranes of the residual liver rapidly decreased, but there was no change in the kidney, lung, and spleen. On the other hand, after unilateral nephrectomy rapid down-regulation of the HGF receptor was clearly evident in the remaining kidney, but not in other organs including the liver. These findings suggest the presence of control mechanisms governing HGF receptor function only in a regenerating organ after injury.
Asunto(s)
Receptores de Superficie Celular/metabolismo , Regeneración/fisiología , Animales , Membrana Celular/metabolismo , Regulación hacia Abajo , Sustancias de Crecimiento/metabolismo , Factor de Crecimiento de Hepatocito , Humanos , Radioisótopos de Yodo , Ratones , Proteínas Proto-Oncogénicas c-met , ARN Mensajero/análisis , Ratas , Distribución TisularRESUMEN
The proliferative potential of hepatocytes in the normal intact liver is highly suppressed, but they proliferate actively after liver injury. In this study, adult rat hepatocytes in primary culture were used to study mechanisms controlling hepatocyte growth in liver regeneration. DNA synthesis in hepatocytes cultured at a low cell density was highly stimulated in response to hepatocyte growth factor (HGF), but this stimulatory effect was not so obvious in hepatocytes cultured at a high cell density. In close parallel to the potency of DNA synthesis, the amounts of 125I-HGF specifically bound to hepatocytes cultured at a low cell density were much greater than in high cell density culture. Scatchard plots revealed that change in the specific binding of 125I-HGF was due to change in the number of high-affinity HGF receptors, but without change in the Kd values. Affinity cross-linking of the HGF receptor with 125I-HGF confirmed the higher expression of HGF receptor on hepatocytes cultured at a lower cell density. Since there was no significant change in the expression of c-met mRNA in hepatocytes cultured at different cell densities, the number of cell surface HGF receptors is probably regulated by post-transcriptional mechanisms. We also found that the rates of HGF-induced down-regulation and recovery of HGF receptors on hepatocytes cultured at a low cell density were much faster than in cases of a high cell density.(ABSTRACT TRUNCATED AT 250 WORDS)
Asunto(s)
Factor de Crecimiento de Hepatocito/metabolismo , Hígado/citología , Proteínas Proto-Oncogénicas/metabolismo , Proteínas Tirosina Quinasas Receptoras/metabolismo , Animales , Recuento de Células , División Celular , Membrana Celular/metabolismo , Células Cultivadas , Cicloheximida/farmacología , ADN/biosíntesis , Regulación hacia Abajo , Hígado/metabolismo , Regeneración Hepática , Masculino , Proteínas Proto-Oncogénicas/aislamiento & purificación , Proteínas Proto-Oncogénicas c-met , Ratas , Ratas Wistar , Proteínas Tirosina Quinasas Receptoras/aislamiento & purificación , Proteínas Recombinantes/metabolismoRESUMEN
The overall incidence of pulmonary embolism (PE) among neurosurgical in-patients, whose ages ranged from 23 to 80, was 0.7%. Our report here is based on five cases of patients with PE. Four of these five patients were over 50 years of age. They had been admitted because of such reasons as brain tumor, spinal cord injury, intracerebral hematoma, and venous sinus thrombosis. Deep vein thrombosis (DVT) was seen in four but none were diagnosed before they had developed PE. Decreased level of consciousness and prolonged bed rest appeared to be common risk factors for PE. Mean duration between admission and onset of PE was 31 days. Although non-specific, tachycardia, tachypnea and hypoxemia were the most common signs and symptoms. As a definitive diagnostic procedure, pulmonary angiography was performed in most of cases. One patient required surgical embolectomy and others were treated with anticoagulation or fibrinolytic agents. In order to prevent recurrent thromboembolic phenomena, ligation of the inferior vena cava was a useful mode of treatment when anticoagulation was not indicated. And this approach seemed to be valid in most neurosurgical patients. We conclude that PE and DVT were not uncommon complications among Japanese neurosurgical patients and they can be treated successfully in collaboration with a cardiovascular surgeon if the diagnosis can be made correctly.
Asunto(s)
Encefalopatías/cirugía , Complicaciones Posoperatorias , Embolia Pulmonar/etiología , Enfermedades de la Médula Espinal/cirugía , Adulto , Anciano , Femenino , Humanos , Masculino , Persona de Mediana Edad , Complicaciones Posoperatorias/tratamiento farmacológico , Complicaciones Posoperatorias/cirugía , Embolia Pulmonar/tratamiento farmacológico , Embolia Pulmonar/cirugía , Terapia Trombolítica , Activador de Plasminógeno de Tipo Uroquinasa/uso terapéutico , Vena Cava Inferior/cirugía , Warfarina/uso terapéuticoAsunto(s)
Hematuria/etiología , Nefrosis Lipoidea/complicaciones , Preescolar , Diagnóstico Diferencial , Membrana Basal Glomerular/ultraestructura , Hematuria/diagnóstico , Humanos , Masculino , Microscopía Electrónica , Microscopía Fluorescente , Nefrosis Lipoidea/diagnóstico , Índice de Severidad de la EnfermedadAsunto(s)
Duramadre/cirugía , Hemangioma Cavernoso del Sistema Nervioso Central/cirugía , Neoplasias Meníngeas/cirugía , Anciano , Craneotomía , Duramadre/patología , Hemangioma Cavernoso del Sistema Nervioso Central/diagnóstico , Hemangioma Cavernoso del Sistema Nervioso Central/patología , Humanos , Imagen por Resonancia Magnética , Masculino , Neoplasias Meníngeas/diagnóstico , Neoplasias Meníngeas/patologíaAsunto(s)
Neoplasias Encefálicas/patología , Bromodesoxiuridina , Glioma/patología , Adolescente , Adulto , Anciano , Anticuerpos Monoclonales , Ciclo Celular , División Celular , Niño , Femenino , Humanos , Masculino , Persona de Mediana EdadAsunto(s)
Proteínas de Homeodominio , Dedos de Zinc , Secuencia de Aminoácidos , Animales , Proteínas del Citoesqueleto/metabolismo , Proteínas de Homeodominio/química , Proteínas de Homeodominio/fisiología , Humanos , Datos de Secuencia Molecular , Paxillin , Fosfoproteínas/metabolismo , Unión Proteica , Proteína Quinasa C/metabolismo , Proteínas Tirosina Quinasas Receptoras/metabolismo , Dedos de Zinc/fisiologíaRESUMEN
Specific binding of 125I-labeled human recombinant HGF to the primary cultured rat hepatocytes or liver plasma membranes was observed to be temperature- and time-dependent. Scatchard analysis indicated the presence of a single class of high affinity receptors with a dissociation constant (Kd) of 24-32 pM, a value in good accord with half maximum dose for HGF activity and a receptor density of about 500-600 sites/cell. Affinity cross-linking of the receptor with 125I-HGF revealed the HGF receptor in rat liver membranes to be a polypeptide of Mr approximately 220,000. After partial hepatectomy, specific binding of 125I-HGF to the membranes of residual livers decreased by 60-70% between 3 and 6 h, and was scanty at 12 h after hepatectomy. After one week, the binding was recovered to the 1.7 fold level in the untreated rat liver. This rapid down-regulation of HGF receptors was also observed in plasma membranes of rat livers in the presence of hepatitis induced by CCl4. We propose that HGF which can be immediately supplied to the liver after hepatic injury will function as a trigger for regeneration of this organ.
Asunto(s)
Sustancias de Crecimiento/metabolismo , Hígado/química , Animales , Tetracloruro de Carbono , Membrana Celular/metabolismo , Células Cultivadas , Enfermedad Hepática Inducida por Sustancias y Drogas/metabolismo , Reactivos de Enlaces Cruzados/metabolismo , ADN/biosíntesis , Regulación hacia Abajo , Factor de Crecimiento Epidérmico/genética , Factor de Crecimiento Epidérmico/metabolismo , Sustancias de Crecimiento/genética , Hepatectomía , Factor de Crecimiento de Hepatocito , Humanos , Hígado/fisiología , Regeneración Hepática , Masculino , Peso Molecular , Ratas , Ratas Endogámicas , Proteínas Recombinantes/genética , Proteínas Recombinantes/metabolismo , Factor de Crecimiento Transformador alfa/genética , Factor de Crecimiento Transformador alfa/metabolismo , Factor de Crecimiento Transformador beta/genética , Factor de Crecimiento Transformador beta/metabolismoRESUMEN
LIM-containing protein kinase 1 (LIMK1) is a serine/threonine kinase with a structure composed of two LIM domains, a PDZ domain, and a protein kinase domain. We examined the subcellular localization of LIMK1 and its variously deleted mutants in HeLa cells by transfection with these cDNAs. Immunofluorescence analysis revealed that the full-length LIMK1 and its mutants deleted with LIM domain or protein kinase domain preferentially localized in the cytoplasm, while the mutants deleted with the PDZ domain or a 52 amino acid region (B region) within the PDZ domain localized mainly in the nucleus. When the normally nuclear cyclin A was fused with the PDZ domain or the B region of LIMK1, it was localized in the cytoplasm of transfected cells. The corresponding region of the PDZ domain of postsynaptic density protein (PSD)-95 had no such function. Additionally, the PDZ domain of LIMK1 had no potential to bind to the C-terminal S/TXV peptides, to which the PSD-95 PDZ domain can bind. Taken together these results suggest that the PDZ domain, particularly the B region, of LIMK1 has a specific function to localize the protein in the cytoplasm. When glutathione S-transferase (GST) fused with the PDZ domain of LIMK1 (GST-PDZ) or GST-PDZ deleted with the B region (GST-PDZ delta B) was microinjected into the nucleus of COS cells, GST-PDZ was almost completely excluded from the nucleus within 30 min, whereas GST-PDZ delta B remained in the nucleus. These findings suggest that the B region of LIMK1 probably has nuclear export signal activity.
Asunto(s)
Secuencia de Aminoácidos/genética , Citoplasma/enzimología , Proteínas de la Membrana/química , Proteínas Quinasas/análisis , Animales , Sitios de Unión/genética , Células COS , Ciclina A/análisis , Ciclina A/genética , Citoplasma/química , Homólogo 4 de la Proteína Discs Large , Guanilato-Quinasas , Humanos , Péptidos y Proteínas de Señalización Intracelular , Quinasas Lim , Datos de Secuencia Molecular , Mutación/genética , Proteínas del Tejido Nervioso/genética , Señales de Localización Nuclear , Proteínas Nucleares/metabolismo , Péptidos/genética , Péptidos/metabolismo , Unión Proteica , Proteínas Quinasas/genética , Proteínas Quinasas/metabolismo , Estructura Terciaria de Proteína , Proteínas Recombinantes de Fusión/genética , Homología de Secuencia de Aminoácido , Fracciones Subcelulares/química , Fracciones Subcelulares/enzimologíaRESUMEN
A case of aneurysm of the middle cerebral artery with congenital porencephaly in the same region is reported. The cyst was opened and the aneurysm was wrapped with a muscle strip. The resected specimen of the cyst wall contained a parenchymal layer with hemosiderinladen macrophages. It is speculated that bleeding from the aneurysm during the perinatal period caused the porencephaly.
Asunto(s)
Encefalopatías/congénito , Quistes/congénito , Aneurisma Intracraneal/complicaciones , Encefalopatías/complicaciones , Encefalopatías/diagnóstico por imagen , Encefalopatías/cirugía , Angiografía Cerebral , Niño , Quistes/complicaciones , Quistes/diagnóstico por imagen , Quistes/cirugía , Humanos , Aneurisma Intracraneal/diagnóstico por imagen , Aneurisma Intracraneal/cirugía , Masculino , Tomografía Computarizada por Rayos XRESUMEN
Hepatocyte growth factor (HGF), a mesenchymal-derived polypeptide, stimulates growth, motility and morphogenesis of various types of cells, most predominantly of epithelial cells. We have now identified an additional biological activity of HGF; this factor probably has a role in early hematopoiesis. We examined the effects of HGF on the growth of various murine hematopoietic progenitor tumor cell lines and found that HGF stimulated DNA synthesis in the myeloid leukemia cell line, NFS-60. The mitogenic effect of HGF on NFS-60 cells was additive with the effect of interleukin 3 (IL-3). On the other hand, HGF had no apparent effect on other myeloid leukemia cell lines examined, such as DA-3 and FDC-P1 cells. Scatchard analysis of specific binding of [125I]HGF revealed expression of a high-affinity HGF receptor on NFS-60 and DA-3 cells, but not on FDC-P1 cells. Expression of c-met mRNA correlated well with the existence of a high-affinity HGF receptor. Since the myeloid leukemia cell lines used are cells in the early stage of myeloid differentiation, HGF may play a role in early hematopoiesis.