نتایج جستجو برای: granulopoiesis

تعداد نتایج: 691  

Journal: :Blood 2014
Steffen Boettcher Rahel C Gerosa Ramin Radpour Judith Bauer Franziska Ampenberger Mathias Heikenwalder Manfred Kopf Markus G Manz

Systemic bacterial infection induces a hematopoietic response program termed "emergency granulopoiesis" that is characterized by increased de novo bone marrow (BM) neutrophil production. How loss of local immune control and bacterial dissemination is sensed and subsequently translated into the switch from steady-state to emergency granulopoiesis is, however, unknown. Using tissue-specific myelo...

Journal: :Haematologica 2015
Julia Kobuch Haissi Cui Barbara Grünwald Paul Saftig Percy A Knolle Achim Krüger

The homeostasis of neutrophil granulocytes can affect the outcome of several inflammation-associated diseases including cancer. The regulation of this homeostasis is still not completely understood. We previously found that elevated systemic levels of tissue inhibitor of metalloproteinases-1 (TIMP-1) induce an increase of neutrophils in the liver, which in turn strongly promotes liver metastasi...

2013
Hideyo Hirai Naoka Kamio Gang Huang Akiko Matsusue Shinpei Ogino Nobuhiko Kimura Sakiko Satake Eishi Ashihara Jiro Imanishi Daniel G. Tenen Taira Maekawa

In contrast to the definitive role of the transcription factor, CCAAT/Enhancer binding protein α (C/EBPα), in steady-state granulopoiesis, previous findings have suggested that granulopoiesis during emergency situations, such as infection, is dependent on C/EBPβ. In this study, a novel lentivirus-based reporter system was developed to elucidate the molecular switch required for C/EBPβ-dependenc...

Journal: :Haematologica 2014
Tatsuya Morishima Ken-ichiro Watanabe Akira Niwa Hideyo Hirai Satoshi Saida Takayuki Tanaka Itaru Kato Katsutsugu Umeda Hidefumi Hiramatsu Megumu K Saito Kousaku Matsubara Souichi Adachi Masao Kobayashi Tatsutoshi Nakahata Toshio Heike

HAX1 was identified as the gene responsible for the autosomal recessive type of severe congenital neutropenia. However, the connection between mutations in the HAX1 gene and defective granulopoiesis in this disease has remained unclear, mainly due to the lack of a useful experimental model for this disease. In this study, we generated induced pluripotent stem cell lines from a patient presentin...

Journal: :Blood 2011
Suparna Nanua Mark Murakami Jun Xia David S Grenda Jill Woloszynek Marie Strand Daniel C Link

Severe congenital neutropenia (SCN) is an inborn disorder of granulopoiesis that in many cases is caused by mutations of the ELANE gene, which encodes neutrophil elastase (NE). Recent data suggest a model in which ELANE mutations result in NE protein misfolding, induction of endoplasmic reticulum (ER) stress, activation of the unfolded protein response (UPR), and ultimately a block in granulocy...

Journal: :Blood 1979
K S Zuckerman P J Quesenberry J Levin R Sullivan

Endotoxin was detected in all erythropoietin preparations tested and was removed from four lots, without loss of erythropoietic activity, by adsorption with limulus amebocyte lysate. Comparison of adsorbed (endotoxin-depleted) and nonadsorbed (endotoxin-containing) erythropoietin preparations demonstrated significant inhibition of CFU-e and BFU-e in vitro by nonadsorbed erythropoietin at concen...

Journal: :Blood 2010
John A Pulikkan Philomina S Peramangalam Viola Dengler Phoenix A Ho Claude Preudhomme Soheil Meshinchi Maximilian Christopeit Oliver Nibourel Carsten Müller-Tidow Stefan K Bohlander Daniel G Tenen Gerhard Behre

The transcription factor, CCAAT enhancer binding protein alpha (C/EBPα), is crucial for granulopoiesis and is deregulated by various mechanisms in acute myeloid leukemia (AML). Mutations in the CEBPA gene are reported in 10% of human patients with AML. Even though the C/EBPα mutants are known to display distinct biologic function during leukemogenesis, the molecular basis for this subtype of AM...

Journal: :Journal of immunology 2000
H T Tan-Pertel L Walker D Browning A Miyamoto G Weinmaster J C Gasson

The Notch transmembrane receptors play important roles in precursor survival and cell fate specification during hematopoiesis. To investigate the function of Notch and the signaling events activated by Notch in myeloid development, we expressed truncated forms of Notch1 or Notch2 proteins that either can or cannot activate the core binding factor 1 (CBF1) in 32D (clone 3) myeloblasts. 32D cells...

Journal: :Haematology and blood transfusion 1979
P Greenberg B Mara

Provision of granulocyte-monocyte colony stimulating activity by human bone marrow (CSAB,) was determined in 21 patients with acute myeloid leukemia (AML) utilizing in vitro culture techniques to assess intramedullary cellular interactions on human granulopoiesis. CSABM production of these patients was compared to that from normal marrow by testing the capacity of conditioned mediums from adher...

Journal: :In vivo 2010
Ulf Harnack Klaus Eckert Iduna Fichtner Gabriele Pecher

Beta-glucans are branched fungal polysaccharide compounds with pleiotropic activating effects on cells of the immune and the hematopoietic system. In this study, the hematopoiesis-promoting effect of an orally administered soluble beta-(1-3),(1-6)-D-glucan and of intravenously (i.v.) injected recombinant human granulocyte colony-stimulating factor (G-CSF/filgrastim) was tested in cyclophosphami...

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