Cytokine receptors and hematopoietic differentiation.

Abstract:

:Colony-stimulating factors and other cytokines signal via their cognate receptors to regulate hematopoiesis. In many developmental systems, inductive signalling determines cell fate and, by analogy with this, it has been postulated that cytokines, signalling via their cognate receptors, may play an instructive role in lineage specification in hematopoiesis. An alternative to this instructive hypothesis is the stochastic or permissive hypothesis. The latter proposes that commitment to a particular hematopoietic lineage is an event that occurs independently of extrinsic signals. It predicts that the role of cytokines is to provide nonspecific survival and proliferation signals. In this review, we look at the role of cytokine receptor signalling in hematopoiesis and consider the evidence for both hypotheses. Data from experiments that genetically manipulate receptor gene expression in vitro or in vivo are reviewed. Experiments in which cytokine receptors were installed in multipotential cells showed that, in some cases, stimulation with the cognate ligand could lead to alterations in lineage output. The creation of genetically manipulated mouse strains demonstrated that cytokine receptors are required for expansion and survival of single lineages but did not reveal a role in lineage commitment. We conclude that hematopoietic differentiation involves mainly stochastic events, but that cytokine receptors also have some instructive role.

journal_name

Oncogene

journal_title

Oncogene

authors

Robb L

doi

10.1038/sj.onc.1210756

subject

Has Abstract

pub_date

2007-10-15 00:00:00

pages

6715-23

issue

47

eissn

0950-9232

issn

1476-5594

pii

1210756

journal_volume

26

pub_type

杂志文章,评审

相关文献

ONCOGENE文献大全
  • Interleukin 1 induces an autocrine loop hepatocyte growth factor/c-Met in murine Kaposi-like spindle cells.

    abstract::Several cytokines, growth factors and the HIV transactivator Tat were shown to be involved in the pathogenesis of Kaposi's sarcoma. BKV/tat transgenic mice develop Kaposi's sarcoma-like lesions, and spindle-shaped cells (TTB) have been derived from these lesions. Here we show that TTB cells co-express hepatocyte growt...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:

    authors: Maier J,Mariotti M,Comoglio PM,Soria MR

    更新日期:1996-09-05 00:00:00

  • DNA binding and selective gene induction by different forms of the p53 protein.

    abstract::P53 is a tumor suppressor gene that plays a crucial role in suppressing tumorigenesis by inducing either cell cycle arrest or apoptosis in cells with DNA damage. In more than 50% of tumors p53 is inactivated by gene mutations. However, there have also been reports of tumor cells in which p53 remains wild type and is p...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1210110

    authors: Mayelzadeh F,Martinez JD

    更新日期:2007-05-10 00:00:00

  • Gene structure of the human MET proto-oncogene.

    abstract::By direct sequencing of cosmids using primers designed from the known cDNA sequence, we identified 19 exons in the human MET proto-oncogene, and sequenced the corresponding 5' and 3' exon-intron junctions. By homology search in the database of the Washington University Genome Sequence Center (GSC), we identified one a...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1201338

    authors: Duh FM,Scherer SW,Tsui LC,Lerman MI,Zbar B,Schmidt L

    更新日期:1997-09-25 00:00:00

  • Repression of androgen receptor mediated transcription by the ErbB-3 binding protein, Ebp1.

    abstract::Members of the ErbB family of receptors have been implicated in regulation of androgen receptor (AR) activity. Ebp1, an ErbB-3 binding protein recently cloned in our laboratory, possesses an LXXLL motif important in mediating interactions with nuclear hormone receptors. Therefore, we sought to determine if Ebp1 could ...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1205638

    authors: Zhang Y,Fondell JD,Wang Q,Xia X,Cheng A,Lu ML,Hamburger AW

    更新日期:2002-08-15 00:00:00

  • Identification of genes differentially expressed in glioblastoma versus pilocytic astrocytoma using Suppression Subtractive Hybridization.

    abstract::Glioblastoma (GBM) is a highly malignant glioma, which has the propensity to infiltrate throughout the brain in contrast to pilocytic astrocytoma (PA) of the posterior fossa, which does not spread and can be cured by surgery. We have used Suppression Subtractive Hybridization to define markers that better delineate th...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1209305

    authors: Colin C,Baeza N,Bartoli C,Fina F,Eudes N,Nanni I,Martin PM,Ouafik L,Figarella-Branger D

    更新日期:2006-05-04 00:00:00

  • G2A is an oncogenic G protein-coupled receptor.

    abstract::G2A is a heptahelical cell surface protein that has recently been described as a potential tumor suppressor, based on its ability to counteract transformation of pre-B cells and fibroblasts by Bcr-Abl, an oncogenic tyrosine kinase. We have isolated cDNAs encoding G2A in the course of screening libraries for clones tha...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1203731

    authors: Zohn IE,Klinger M,Karp X,Kirk H,Symons M,Chrzanowska-Wodnicka M,Der CJ,Kay RJ

    更新日期:2000-08-10 00:00:00

  • Detection of novel mRNA splice variants of human ING4 tumor suppressor gene.

    abstract::Inhibitor of growth (ING)4, member of a gene family encoding potential tumor suppressors, is implicated as a repressor of angiogenesis and tumor growth and suppresses loss of contact inhibition in vitro. Here, we report that ING4 undergoes alternative splicing. Expression analysis identified novel ING4 spliced variant...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1210335

    authors: Raho G,Miranda C,Tamborini E,Pierotti MA,Greco A

    更新日期:2007-08-09 00:00:00

  • The protein-tyrosine phosphatase DEP-1 modulates growth factor-stimulated cell migration and cell-matrix adhesion.

    abstract::Density-enhanced protein-tyrosine phosphatase-1 (DEP-1 also CD148) is a transmembrane molecule with a single intracellular PTP domain. It has recently been proposed to function as a tumor suppressor. We have previously shown that DEP-1 dephosphorylates the activated platelet-derived growth factor (PDGF) beta-receptor ...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1206652

    authors: Jandt E,Denner K,Kovalenko M,Ostman A,Böhmer FD

    更新日期:2003-07-03 00:00:00

  • Mutations that disrupt PHOXB interaction with the neuronal calcium sensor HPCAL1 impede cellular differentiation in neuroblastoma.

    abstract::Heterozygous germline mutations in PHOX2B, a transcriptional regulator of sympathetic neuronal differentiation, predispose to diseases of the sympathetic nervous system, including neuroblastoma and congenital central hypoventilation syndrome (CCHS). Although the PHOX2B variants in CCHS largely involve expansions of th...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/onc.2013.290

    authors: Wang W,Zhong Q,Teng L,Bhatnagar N,Sharma B,Zhang X,Luther W 2nd,Haynes LP,Burgoyne RD,Vidal M,Volchenboum S,Hill DE,George RE

    更新日期:2014-06-19 00:00:00

  • Detailed analysis of the basic domain of the E2F1 transcription factor indicates that it is unique among bHLH proteins.

    abstract::The E2F1 transcription factor binds to sites within the promoters of a number of cell cycle regulated genes through a basic-helix-loop-helix motif (bHLH). It is shown here that the basic region of E2F1 is distinct from that of all other bHLH proteins. The center of the basic region contains a helix breaking proline-gl...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:

    authors: Jordan KL,Haas AR,Logan TJ,Hall DJ

    更新日期:1994-04-01 00:00:00

  • Identification of fyn-encoded proteins in normal human blood cells.

    abstract::We have previously reported that carboxyl terminal truncations of the normal human fyn gene, a member of the src subfamily, can transform immortal mouse fibroblasts to full malignancy. In search of evidence which suggests the possible activation of the human fyn gene, we have screened DNAs and RNAs from a number of hu...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:

    authors: Kawakami Y,Furue M,Kawakami T

    更新日期:1989-03-01 00:00:00

  • AP2α controls the dynamic balance between miR-126&126* and miR-221&222 during melanoma progression.

    abstract::Accumulating evidences have shown the association between aberrantly expressed microRNAs (miRs) and cancer, where these small regulatory RNAs appear to dictate the cell fate by regulating all the main biological processes. We demonstrated the responsibility of the circuitry connecting the oncomiR-221&222 with the tumo...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/onc.2015.357

    authors: Felli N,Errico MC,Pedini F,Petrini M,Puglisi R,Bellenghi M,Boe A,Felicetti F,Mattia G,De Feo A,Bottero L,Tripodo C,Carè A

    更新日期:2016-06-09 00:00:00

  • Mutation of beta-catenin is an early event in chemically induced mouse hepatocellular carcinogenesis.

    abstract::beta-catenin activation, and subsequent upregulation of Wnt-signaling, is an important event in the development of certain human and rodent cancers. Recently, mutations in the beta-catenin gene in the region of the serine-threonine glycogen kinase (GSK)-3beta phosphorylation target sites have been identified in hepato...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1202858

    authors: Devereux TR,Anna CH,Foley JF,White CM,Sills RC,Barrett JC

    更新日期:1999-08-19 00:00:00

  • TPX2/Aurora kinase A signaling as a potential therapeutic target in genomically unstable cancer cells.

    abstract::Genomic instability is a hallmark feature of cancer cells, and can be caused by defective DNA repair, for instance due to inactivation of BRCA2. Paradoxically, loss of Brca2 in mice results in embryonic lethality, whereas cancer cells can tolerate BRCA2 loss. This holds true for multiple DNA repair genes, and suggests...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/s41388-018-0470-2

    authors: van Gijn SE,Wierenga E,van den Tempel N,Kok YP,Heijink AM,Spierings DCJ,Foijer F,van Vugt MATM,Fehrmann RSN

    更新日期:2019-02-01 00:00:00

  • MAOA-mediated reprogramming of stromal fibroblasts promotes prostate tumorigenesis and cancer stemness.

    abstract::The tumor microenvironment plays a critical role in prostate cancer (PC) development and progression. Inappropriate activation of the stroma potentiates the growth and transformation of epithelial tumor cells. Here, we show that upregulation of monoamine oxidase A (MAOA), a mitochondrial enzyme that degrades monoamine...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/s41388-020-1217-4

    authors: Li J,Pu T,Yin L,Li Q,Liao CP,Wu BJ

    更新日期:2020-04-01 00:00:00

  • v-Src activates both protein kinase C-dependent and independent signaling pathways in murine fibroblasts.

    abstract::Activating the protein-tyrosine kinase activity of v-Src rapidly induced expression of the two 'primary response' genes, TIS10 and Egr-1, in Balb/c 3T3 cells. Depleting cells of protein kinase C (PKC) by prolonged exposure to 12-O-tetradecanoylphorbol 13-acetate (TPA), blocked v-Src-induced TIS10 expression, but had n...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:

    authors: Qureshi SA,Joseph CK,Rim M,Maroney A,Foster DA

    更新日期:1991-06-01 00:00:00

  • A ubiquitin ligase, skeletrophin, is a negative regulator of melanoma invasion.

    abstract::Skeletrophin (mindbomb homolog 2 (MIB2)) is a RING (Really Interesting New Gene) finger-dependent ubiquitin ligase, which targets the intracellular region of Notch ligands. A previous immunohistochemical study demonstrated that skeletrophin was downregulated in many melanomas. In the present study, we have identified ...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1209688

    authors: Takeuchi T,Adachi Y,Sonobe H,Furihata M,Ohtsuki Y

    更新日期:2006-11-09 00:00:00

  • The large E1B protein together with the E4orf6 protein target p53 for active degradation in adenovirus infected cells.

    abstract::It has recently been shown that an adenovirus mutant lacking expression of the large E1B protein (deltaE1B) selectively replicates in p53 deficient cells. However, apart from the large E1B protein the adenovirus early region encodes the E1A and E4orf6 proteins which also have been reported to affect p53 expression as ...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1201540

    authors: Steegenga WT,Riteco N,Jochemsen AG,Fallaux FJ,Bos JL

    更新日期:1998-01-22 00:00:00

  • Delayed cyclin B1 expression during the G2 arrest following DNA damage.

    abstract::Exposure of cells to DNA damaging agents results in a G2 arrest. Exposure of HeLa cells to camptothecin, etoposide or nitrogen mustard for 1 h in S phase resulted in delayed expression of cyclin B1 mRNA during the G2 arrest. Initially the levels of cyclin B1 protein were low as well; however, with extended time the ce...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:

    authors: Maity A,Hwang A,Janss A,Phillips P,McKenna WG,Muschel RJ

    更新日期:1996-10-17 00:00:00

  • EGFR mutants found in non-small cell lung cancer show different levels of sensitivity to suppression of Src: implications in targeting therapy.

    abstract::Mutations in epidermal growth factor receptor (EGFR) kinase domain associate with clinical responses to EGFR inhibitors and are frequently observed in non-small cell lung cancer (NSCLC) patients in East Asian populations. Clinically identified EGFR mutations cause constitutive receptor activation. The activating mecha...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1210684

    authors: Fu YN,Yeh CL,Cheng HH,Yang CH,Tsai SF,Huang SF,Chen YR

    更新日期:2008-02-07 00:00:00

  • FOXA1 inhibits prostate cancer neuroendocrine differentiation.

    abstract::Neuroendocrine prostate cancer (NEPC) has increasingly become a clinical challenge. The mechanisms by which neuroendocrine (NE) cells arises from prostate adenocarcinoma cells are poorly understood. FOXA1 is a transcription factor of the forkhead family that is required for prostate epithelial differentiation. In this...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/onc.2017.50

    authors: Kim J,Jin H,Zhao JC,Yang YA,Li Y,Yang X,Dong X,Yu J

    更新日期:2017-07-13 00:00:00

  • p73 is transcriptionally regulated by DNA damage, p53, and p73.

    abstract::p73 is a member of the p53 family. Recent studies have shown that DNA damage can stabilize p73 protein and enhance p73-mediated apoptosis in a c-Abl dependent manner. To determine what regulates p73 transcriptionally, we analysed the expression of p73 in several cell lines following genotoxic stresses. We found that p...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1204149

    authors: Chen X,Zheng Y,Zhu J,Jiang J,Wang J

    更新日期:2001-02-08 00:00:00

  • Mel-CAM-specific genetic suppressor elements inhibit melanoma growth and invasion through loss of gap junctional communication.

    abstract::Normal human melanocytes are interspersed singly among keratinocytes along the basement membrane of the epidermis, whereas melanoma cells readily adhere to each other during invasion of the dermis or distant organs. The tumorigenic and metastatic phenotype of melanoma cells often correlates with increased expression o...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1204616

    authors: Satyamoorthy K,Muyrers J,Meier F,Patel D,Herlyn M

    更新日期:2001-08-02 00:00:00

  • Stabilization of prolactin receptor in breast cancer cells.

    abstract::The role of the hormone prolactin (PRL) in the pathogenesis of breast cancer is mediated by its cognate receptor (PRLr). Ubiquitin-dependent degradation of the PRLr that negatively regulates PRL signaling is triggered by PRL-mediated phosphorylation of PRLr on Ser349 followed by the recruitment of the beta-transducin ...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1209214

    authors: Li Y,Clevenger CV,Minkovsky N,Kumar KG,Raghunath PN,Tomaszewski JE,Spiegelman VS,Fuchs SY

    更新日期:2006-03-23 00:00:00

  • Methyltransferase inhibition induces p53-dependent apoptosis and a novel form of cell death.

    abstract::We have analysed the importance of proper substrate methylation by S-adenosylmethionine-dependent methyltransferases for cell survival and cell cycle progression. We show that treatment of cells with the methyltransferase inhibitor adenosine dialdehyde (AdOx) causes cell cycle arrest and death in different cell types....

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1208855

    authors: Schwerk C,Schulze-Osthoff K

    更新日期:2005-10-27 00:00:00

  • Phosphorylation at serine 28 and acetylation at lysine 9 of histone H3 induced by trichostatin A.

    abstract::Trichostatin A (TSA), a histone deacetylase inhibitor, strongly increases acetylation of the N-terminal tails of histone H3. Many studies have correlated the function of TSA with the hyperacetylation of histone. Although histone H3 is known to be phosphorylated, the effect of acetylation on phosphorylation is not know...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1206507

    authors: Zhong S,Goto H,Inagaki M,Dong Z

    更新日期:2003-08-14 00:00:00

  • ACTL6A suppresses p21Cip1 expression to enhance the epidermal squamous cell carcinoma phenotype.

    abstract::Epidermal squamous cell carcinoma (SCC) is a common and highly invasive form of cancer. SCC arises due to ultraviolet light exposure and is associated with increased expression of pro-cancer genes and reduced expression of cancer suppressors. Actin-Like Protein 6A (ACTL6A, BAF53a) is an important protein subunit of th...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/s41388-020-1371-8

    authors: Shrestha S,Adhikary G,Xu W,Kandasamy S,Eckert RL

    更新日期:2020-09-01 00:00:00

  • Functional capabilities of molecular network components controlling the mammalian G1/S cell cycle phase transition.

    abstract::The molecular interactions implicated in the mammalian G1/S cell cycle phase transition comprise a highly nonlinear network which can produce seemingly paradoxical results and make intuitive interpretations unreliable. A new approach to this problem is presented, consisting of (1) a convention of unambiguous reaction ...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1201608

    authors: Kohn KW

    更新日期:1998-02-26 00:00:00

  • Interferons alpha and gamma induce p53-dependent and p53-independent apoptosis, respectively.

    abstract::Type I interferon (IFN) enhances the transcription of the tumor suppressor gene p53. To elucidate the molecular mechanism mediating IFN-induced apoptosis, we analysed programmed cell death in response to type I (IFNalpha) or type II (IFNgamma) treatment in relation to p53 status. In two cell lines (MCF-7, SKNSH), IFNa...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1208204

    authors: Porta C,Hadj-Slimane R,Nejmeddine M,Pampin M,Tovey MG,Espert L,Alvarez S,Chelbi-Alix MK

    更新日期:2005-01-20 00:00:00

  • Differential requirements for ERK1/2 and P38 MAPK activation by thrombin in T cells. Role of P59Fyn and PKCepsilon.

    abstract::Activation of the mitogen-activated protein kinase (MAPK) cascade is a well documented mechanism for the G-protein-coupled receptors. Here, we have analysed the requirements for ERKs and p38 MAPK activation by thrombin in Jurkat T cells. We show that thrombin-mediated ERKs activation requires both PTK and PKC activiti...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1204266

    authors: Maulon L,Mari B,Bertolotto C,Ricci JE,Luciano F,Belhacene N,Deckert M,Baier G,Auberger P

    更新日期:2001-04-12 00:00:00