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© The Rockefeller University Press,
0021-9525/1999//421 $5.00
The Journal of Cell Biology, Volume 145, Number 3,
, 1999 421-424
Mini-Review |
Import(ance) of Growth Factors in(to) the Nucleus
Department of Molecular Cell Biology, University of Utrecht, Utrecht, The Netherlands
Abbreviations used in this paper: GF, growth factor; HSPG, heparan sulfate proteoglycan; NLS, nuclear localization sequence; R, receptor.
Address correspondence to Margit Keresztes, Department of Biochemistry, Albert Szent-Györgyi Medical University, 6701 Szeged, POB 415, Hungary. Tel.: 36-62-455-096. Fax: 36-62-455-097. E-mail: margo{at}biochem.szote.u-szeged.hu
POLYPEPTIDE growth factors (GFs)1 play a fundamental role during embryogenesis and regeneration (e.g., wound healing) by stimulating proliferation and differentiation of certain cell populations. Some GFs can be responsible also for malignant transformation and tumor growth (e.g., FGF-4: hst1 oncogene). GF receptors (GFRs) are generally known as plasma membrane proteins which "send" signals to the nucleus principally via the MAPK and the JAK-STAT pathways (Karin and Hunter, 1995). However, in the past few years data were accumulating to suggest that, surprisingly, nuclear targeting and action of GFs and GF receptors could occur as well. This alternative or complementary signaling pathway appears to be involved in the induction of cell proliferation. In addition, nuclear GF–GFR complexes may participate in the activation of cell line–specific genes as well. Since by far the largest body of data has been published in relation to FGF-1 and -2 (aFGF and bFGF), we have focused here on the nuclear role of these GFs.
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Mitogenic Effect and Developmental Appearance of Nucleus-associated GFs |
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 Top Mitogenic Effect and... Nuclear Targeting of GFs...Normal Cells: Anchorage...References |
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The presence of radiolabeled, externally added aFGF in the nuclear fraction appeared to correlate with stimulation of DNA synthesis in a concentration-dependent manner in NIH 3T3 cells (with a submaximal [3H]thymidine incorporation value at 10 ng/ml FGF-1). Correlation between nuclear association of aFGF and DNA synthesis was demonstrated also in diphtheria toxin–resistant U2 Os Dr1 cells. Although these cells lack aFGF receptors, they were able to internalize aFGF via their cell surface toxin receptors, if the GF was fused to the diphtheria toxin fragments. After extracellular administration, the aFGF-toxin label was detected in the nuclear fraction. At the same time, DNA synthesis was found to rise about fourfold (at a fairly low, 5 ng/ml aFGF-toxin). However, no significant increase in the number of cells was observed. Therefore, it appears that although nuclear action of aFGF seems to be sufficient for triggering DNA synthesis, FGFR is indispensable for other processes of cell proliferation (Wiedlocha et al., 1994). Consistent with this idea, DNA synthesis was accompanied by cell proliferation only in cells which possess aFGF receptors or if the toxin-resistant cells were transfected with a FGFR (Wiedlocha et al., 1996).
However, one has to keep in mind that cell lines, transfected cells, and tumor cells most probably do not behave and cannot be considered as normal cells. Nonetheless, cell proliferation rate and nuclear association of bFGF was reported to change in parallel not only in glioma cells for example, which express transfection-derived endogenous FGF-2, but also in primary cultures of human astrocytes stimulated with extracellular bFGF (concentration range: 0.09–2.5 nM) (Joy et al., 1997). These observations support the idea that nuclear translocation of GFs could be related to mitogenesis in normal, nontransformed cells as well.
Uptake of extracellular bFGF to the nucleus and to the nucleolus was found to occur only in late G1 phase of the cell cycle in growing aortic endothelial (ABAE) cells, both by immunocytochemistry and by analysis of radioiodinated cell fractions (Baldin et al., 1990). Nuclear association of FGF-2 was also observed in mid-late G1 phase in proliferating epiphyseal plate chondrocytes (Kilkenny and Hill, 1996), suggesting a controlled nuclear entry of GFs around the restriction point of the cell cycle.
It is important to note that autocrine and intracrine FGF types can have different effects, which are related to their partially different sequence and to their characteristic site of action. From the four different forms of human FGF-2, the low molecular mass form (with 18 kD) is an autocrine/ paracrine one. The three high molecular mass forms (with 21–22, 22.5, and 24 kD, respectively) are the intracrine ones generated by alternative translation initiation at CUG codon, through an internal ribosome entry process regulated by a cis-acting mechanism (Vagner et al., 1996). These intracrine forms, which have a longer, arginine-rich NH2-terminal with at least two possible short nuclear localization sequences (NLSs) (Gly-Arg-Gly-Arg-Gly-Arg), are preferentially targeted to the nucleus (Quarto et al., 1991). In contrast, the 18-kD form has only a weak or cryptic short NLS, and is found predominantly in the cytoplasm (Quarto et al., 1991; Davis et al., 1997). Only the short bFGF form can be released from the cell, and can, therefore, interact with the plasma membrane FGFR. Surprisingly, when intracrine bFGF types were expressed in NIH 3T3 cells, high proliferation rates and growth in soft agar were observed, even in the presence of mutant cell surface bFGF receptors lacking the Tyr kinase domain (Bikfalvi et al., 1995). This reflects a plasma membrane receptor–independent pathway, presumably via formation of complexes between intracrine GFs and intracellular receptors (see below). In vascular smooth muscle cell lines expressing different human bFGFs, the intracrine bFGF forms appeared to be significantly more effective in augmenting the rate of DNA synthesis than the autocrine one (Davis et al., 1997). Moreover, the continuous proliferation of two glioma cell lines is suggested to be related to the constitutive presence of endogenous FGF-2 in nuclei; these cells were nonresponsive to extracellular GFs (Joy et al., 1997). Synthesis of CUG-initiated forms could be induced also in primary human skin fibroblasts, producing normally the short bFGF form almost exclusively, by heat shock (45°C, 15–60 min) and by oxidative stress, which is probably due to translational activation (Vagner et al., 1996).
Developmental studies indicated that FGF-2, known as a maternal signal involved in mesoderm induction in amphibians, brings about mesoderm induction via Src-kinase Laloo (Weinstein et al., 1998) and MAP kinase (Umbhauer et al., 1995). However, nuclear bFGF may be involved in other specific developmental phenomena, since nuclear association of bFGF becomes restricted to some cell populations during embryogenesis. In the mid-blastula stage, FGF-2 was demonstrated clearly in the nuclei of the animal hemisphere of Xenopus; in the prelarval embryo, nuclear bFGF was shown in most head regions (including the brain) and particularly in some muscle cells of the trunk region (immunocytochemical study by Song and Slack, 1994). This is consistent with the well-known stimulatory effects of bFGF on myoblast proliferation (Burgess and Maciag, 1989) and on proliferation plus differentiation of neuroblasts and glial precursor cells (M.K. Stachowiak et al., 1997). In early chicken embryos, nuclear FGF-2 isoforms were observed in most cells of the prestreak blastodiscs during hypoblast formation and mesoderm induction. Only the hypoblasts and the blastocoelic cells seemed to maintain their nuclear immunostaining during primitive streak formation and with the onset of gastrulation (Riese et al., 1995). In later phases, only a small proportion of limb bud cells, most likely migrating myoblasts, and differentiating kidney podocytes were shown to have considerable nuclear FGF-2 (immunohistochemical study by Dono and Zeller, 1994).
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Nuclear Targeting of GFs and GFRs |
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TopMitogenic Effect and...Nuclear Targeting of GFs...Normal Cells: Anchorage...References |
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According to the emerging view, NLS-bearing GFs like FGFs presumably facilitate the nuclear import of their receptors. Theoretically, GFs do not need NLS to enter the nucleus, since the molecular "sieves" of nuclear pores demand it only from compounds >40–45 kD. Possession of NLSs by low molecular mass GFs implies that this may be necessary for the nuclear import of their receptors which can be transported "piggyback" to the nucleus in association with NLS-bearing ligands (Jans, 1994; Jans and Hassan, 1998). The concept that plasma membrane GFRs could enter the nucleus upon extracellular GF stimulation is supported by the accurate study of Maher (1996), who demonstrated a dose- and time-dependent increase of nucleus-associated FGFR-1 immunoreactivity in Swiss 3T3 fibroblasts (onset: within 10 min, max: 1 h; concentration: 5–15–50 ng/ml). Moreover, the FGFR-1 in the nuclear fraction was shown to bear the impermeable biotin label of the cell surface proteins and was proven to be of full length, verifying its plasma membrane origin. Even intracrine FGFs may enter the nucleus in complex with intracellular receptors. Consistent with this idea, several truncated forms of FGFR-1 and FGFR-2 have been described, which are devoid of the transmembrane region (Givol and Yayon, 1992). Furthermore, a truncated FGFR3 variant missing the transmembrane part and half of the final Ig-like domain was shown to be characteristically associated with cell nuclei in breast epithelial cell lines by immunocytochemistry (Johnston et al., 1995).
Considering the role of high-affinity GF receptors in nuclear targeting, they are probably prerequisite for the intracellular transport of GFs to the perinuclear region during receptor-mediated endocytosis. According to the studies of Prudovsky et al. (1996) on transfected L6 myoblasts, the first Ig-like loop in type 1 FGFRs may facilitate the transport of exogenous FGF-1 to the perinuclear area, as mostly the 
, 3-loop receptor isoforms possessing this domain (and not the β isoforms lacking it) were demonstrated in the nuclear/perinuclear fraction. N-glycosylation seems to be also important, as tunicamycin treatment significantly reduced the presence of the receptor forms in the nuclear/perinuclear fraction. This can be interpreted on the basis of NLS-independent, but sugar-dependent nuclear import mechanism described by Duverger et al. (1995), as GFRs are glycoproteins (M.K. Stachowiak et al., 1997).
Regarding FGFs, possible involvement of low-affinity saccharide receptors in nuclear translocation cannot be ruled out. Heparan sulfate proteoglycans (HSPGs) with highly O-sulfated oligosaccharide chains are well known to play a crucial role in the formation and in the maintenance of the active FGFR–a/bFGF complexes at the plasma membrane (Luo et al., 1996). Perlecan, a basal lamina proteoglycan (Aviezer et al., 1994), syndicans, and glypican (Steinfeld et al., 1996) proved to be effective in stimulating FGF–FGFR interaction. It is thought that HSPG and extracellular bFGF bound to FGFR might be cotranslocated to the nucleus; HSPG could stabilize the complex and protect it from degradation in the endocytotic vesicles and in the lysosomes (Reiland and Rapraeger, 1993). Since glypican was observed in association with cell nuclei (in rat neurons and in glioma cells) and, moreover, it was shown to have functional NLS (Liang et al., 1997), this gives further credence to the mentioned idea.
In NIH 3T3 cells, the constitutively activated FGFR-3 mutant kinase domains in linkage with the plasma membrane appeared to be sufficient to trigger cell proliferation and transformation, in contrast to wild-type kinase domains, or to activated kinase domains targeted to the nucleus or to the cytoplasm (Webster and Donoghue, 1997). However, in astrocyte and glioma cultures, cell proliferation appeared to correlate with the nuclear presence of FGFR-1. Continuously proliferating glioma cells, unresponsive to external FGF, displayed constitutive nuclear association of FGFR-1. In contrast, astrocytes had decreasing nuclear appearance of FGFR-1 in parallel to increasing cell density in cultures approaching confluency. Furthermore, enhanced cell proliferation rate could be achieved in glioma cells lacking FGFR-1 by transfecting them with the full-length receptor cDNA; thereafter, immunoreactivity of FGFR-1 was seen predominantly in association with the nucleus (E.K. Stachowiak et al., 1997). Both in astrocytes and in bovine adrenal medullary cells, the nuclear FGFR was shown to retain kinase activity. With this observation, we arrived at a basic, but currently unresolved question.
How could GFs and GFRs act in the nucleus? Nuclear FGFR kinase activity is thought to have no significant role in the induction of cell proliferation (Webster and Donoghue, 1997). However, bFGF may be involved in induction of ribosomal gene transcription via stimulation of casein kinase-2, which is known to regulate nucleolin, a major component of the nucleolus implicated in ribosome biogenesis. Using nuclear extracts of FM3A cells and purified proteins, FGF-2 was shown to bind CK-2 and stimulate its activity, resulting in an increased phosphorylation of nucleolin (Bonnet et al., 1996). (Enhancement of CK-2 activity reached its maximum at 10-7 M FGF-2 concentration, which was calculated to be a possible bFGF concentration in the nucleus.) Supporting these observations, rRNA was found to increase severalfold upon addition of bFGF (0.1–1 nM) to isolated nuclei from quiescent ABAE cells (Bouche et al., 1987). Furthermore, GF–GFR complexes may cotransport intranuclearly acting molecules to the nucleus, via binding to the receptor, as was suggested for IFN-
–IFN receptor complex and STAT by Johnson et al. (1998).
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Normal Cells: Anchorage-dependent GF Transport to the Nucleus? |
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TopMitogenic Effect and...Nuclear Targeting of GFs...Normal Cells: Anchorage...References |
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It is intriguing to hypothesize that actin is involved not only in endocytosis and in the transport of endosomes to the perinuclear area (Durrbach et al., 1996), but also in the precise nuclear targeting of GF–GFR complexes from the perinuclear cytoplasm, since actin is known to be present in abundance in cell nuclei, both in the chromatin and in the nuclear matrix fraction (Capco et al., 1982). Furthermore, there is evidence that a GF receptor, the EGFR, is a (direct) actin-binding protein (den Hartigh et al., 1992); other GFRs may be linked to actin indirectly, via actin-binding proteins, during their nuclear translocation.
It should be noted in this context that extracellular matrix-dependent cytoskeletal organization supervises GF action on proliferation of normal cells, reflected in the well-known phenomenon of anchorage-dependent growth. Cell division is generally preceded by extensive cell spreading (Alberts et al., 1994). Spreading is probably necessary for nuclear translocation of GF–GFR complex in normal cells, since only astrocytes in subconfluent cultures (and not the ones in confluent cultures in short of extracellular surface) were observed to have nuclear-associated bFGF and FGFR-1. On the contrary, in continuously growing glioma cells, nuclear appearance of FGF-2 and FGFR-1 was constitutive and was largely independent of cell density (Joy et al., 1997; E.K. Stachowiak et al., 1997). Finally, bFGF gene is continuously activated in glioma cells irrespective of cell density, whereas in astrocytes bFGF transcription is induced by subconfluency (Moffett et al., 1996).
All in all, it seems that a portion of internalized exogenous FGFs plus their receptors may escape degradation and could be transported to the cell nucleus. Nuclear GF– GFR complexes appear to stimulate cell proliferation in certain conditions in several cell types; in addition, activation of cell line–specific genes may occur in some differentiating cells. Continuous proliferation of transformed cells could be partially due to the continuous nuclear presence of GFs and GFRs. Obviously, much work has to be done to elucidate details of the nuclear targeting of GF–GFR complexes and to be able to understand their nuclear action fully.
Submitted: 3 February 1998
Revised: 3 March 1999
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References |
|---|
|
TopMitogenic Effect and...Nuclear Targeting of GFs...Normal Cells: Anchorage...References |
|---|
Alberts, B., B. Dennis, J. Lewis, M. Raff, K. Roberts, and J.D. Watson. 1994. Normal animal cells in culture need anchorage in order to pass start. In Molecular Biology of the Cell. Garland Publishing, London and New York. 898–900.
Aviezer D, Hecht D, Safran M, Elsinger M, David G & Yayon A. Perlecan, basal lamina proteoglycan, promotes basic fibroblast growth factor-receptor binding, mitogenesis, and angiogenesis, Cell, 1994, 79, 1005–1013.[Medline]
Baldin V, Roman A-M, Bosc-Bierne I, Amalric F & Bouche G. Translocation of bFGF to the nucleus is G1phase cell cycle specific in bovine aortic endothelial cells, EMBO (Eur Mol Biol Organ) J, 1990, 9, 1511–1517.[Medline]
Bikfalvi A, Klein S, Pintucci G, Quarto N, Mignatti P & Rifkin DB. Differential modulation of cell phenotype by different molecular weight forms of basic fibroblast growth factor: possible intracellular signaling by the high molecular weight forms, J Cell Biol, 1995, 129, 233–243.
Bonnet H, Filhol O, Truchet I, Brethenou P, Cochet C, Amalric F & Bouche G. Fibroblast growth factor-2 binds to the regulatory β subunit of CK2 and directly stimulates CK2 activity toward nucleolin, J Biol Chem, 1996, 271, 24781–24787.
Bouche G, Gas N, Prats H, Baldin V, Tauber J-P, Teissie J & Amalric F. Basic fibroblast growth factor enters the nucleolus and stimulates the transcription of ribosomal genes in ABAE cells undergoing Go-G1transition, Proc Natl Acad Sci USA, 1987, 84, 6770–6774.
Burgess W & Maciag T. The heparin-binding (fibroblast) growth factor family of proteins, Annu Rev Biochem, 1989, 58, 575–606.[Medline]
Burwen SJ & Jones AL. The association of polypeptide hormones and growth factors with the nuclei of target cells, Trends Biochem Sci, 1987, 12, 159–162.
Capco DG, Wan KM & Penman S. The nuclear matrix: three-dimensional architecture and protein composition, Cell, 1982, 29, 847–858.[Medline]
Davis MG, Zhou M, Ali S, Coffin D, Doetschman T & Dorn GW II. Intracrine and autocrine effects of basic fibroblast growth factor in vascular smooth muscle cells, J Mol Cardiol, 1997, 29, 1061–1072.[Medline]
Dono R & Zeller R. Cell-type-specific nuclear translocation of fibroblast growth factor-2 isoforms during chicken kidney and limb morphogenesis, Dev Biol, 1994, 163, 316–330.[Medline]
Durrbach A, Louvard D & Coudrier E. Actin filaments facilitate two steps of endocytosis, J Cell Sci, 1996, 109, 457–465.[Abstract]
Duverger E, Pellerin-Mendes C, Mayer R, Roche A-C & Monsigny M. Nuclear import of glycoconjugates is distinct from the classical NLS pathway, J Cell Sci, 1995, 108, 1325–1332.[Abstract]
Givol D & Yayon A. Complexity of FGF receptors: genetic basis for structural diversity and functional specificity, FASEB (Fed Am Soc Exp Biol) J, 1992, 6, 3362–3369.[Abstract]
den Hartigh JC & van Bergen PMP. en Henegouwen, A.J. Verkleij, and J. Boonstra. The EGF receptor is an actin-binding protein, J Cell Biol, 1992, 119, 349–355.
Huang J, Mohammadi M, Rodrigues GA & Schlessinger J. Reduced activation of RAF-1 and MAP kinase by a fibroblast growth factor receptor mutant deficient in stimulation of phosphatidylinositol hydrolysis, J Biol Chem, 1995, 270, 5065–5072.
Jans DA. Nuclear signaling pathways for polypeptide ligands and their membrane receptors? , FASEB (Fed Am Soc Exp Biol) J, 1994, 8, 841–847.[Abstract]
Jans DA & Hassan G. Nuclear targeting by growth factors, cytokines, and their receptors: a role in signaling? , BioEssays, 1998, 20, 400–411.[Medline]
Johnson HM, Torres BA, Green MM, Szente BE, Siler KI, Larkin J III & Subramaniam PS. Cytokine-receptor complexes as chaperones for nuclear translocation of signal transducers, Biochem Biophys Res Commun, 1998, 244, 607–614.[Medline]
Johnston CL, Cox HC, Gomm JJ & Coombes RC. Fibroblast growth factor receptors (FGFRs) localize in different cellular compartments: a splice variant of FGFR-3 localizes to the nucleus, J Biol Chem, 1995, 270, 30643–30650.
Joy A, Moffett J, Neary K, Mordechai E, Stachowiak EK, Coons S, Rankin-Shapiro J, Florkiewicz RZ & Stachowiak MK. Nuclear accumulation of FGF-2 is associated with proliferation of human astrocytes and glioma cells, Oncogene, 1997, 14, 171–183.[Medline]
Karin M & Hunter T. Transcriptional control by protein phosphorylation: signal transmission from the cell surface to the nucleus, Curr Biol, 1995, 5, 747–757.[Medline]
Kilkenny D & Hill DJ. Perinuclear localization of an intracellular binding protein related to the fibroblast growth factor (FGF) receptor 1 is temporally associated with the nuclear trafficking of FGF-2 in proliferating epiphyseal growth plate chondrocytes, Endocrinology, 1996, 137, 5078–5089.[Abstract]
Liang Y, Haring M, Roughley PJ, Margolis RK & Margolis RU. Glypican and biglycan in the nuclei of neurons and glioma cells: presence of functional nuclear localization signals and dynamic changes in glypican during the cell cycle, J Cell Biol, 1997, 139, 851–864.
Lobie PE, Mertani H, Morel G, Morales-Bustos O, Norstedt G & Waters MJ. Receptor-mediated nuclear translocation of growth hormone, J Biol Chem, 1994, 269, 21330–21339.
Luo Y, Gabriel JL, Wang F, Zhan X, Maciag T, Kan M & McKeehan WL. Molecular modeling and deletion mutagenesis implicate the nuclear translocation sequence in structural integrity of fibroblast growth factor-1, J Biol Chem, 1996, 271, 26876–26883.
Maher PA. Nuclear translocation of fibroblast growth factor (FGF) receptors in response to FGF-2, J Cell Biol, 1996, 134, 529–536.
Mason IJ. The ins and outs of fibroblast growth factors, Cell, 1994, 78, 547–552.[Medline]
Moffett J, Kratz E, Florkiewicz R & Stachowiak MK. Promoter regions involved in density-dependent regulation of basic fibroblast growth factor gene expression in human astrocytic cells, Proc Natl Acad Sci USA, 1996, 93, 2470–2475.
Prochiantz A & Theodore L. Nuclear/growth factors, BioEssays, 1995, 17, 39–44.[Medline]
Prudovsky IA, Savion N, La Vallee TM & Maciag T. The nuclear trafficking of extracellular fibroblast growth factor (FGF)-1 correlates with the perinuclear association of the FGF receptor-1 isoforms but not the FGF receptor-1β isoforms, J Biol Chem, 1996, 271, 14198–14205.
Quarto N, Finger FP & Rifkin DB. The NH2-terminal extension of high molecular weight bFGF is a nuclear targeting signal, J Cell Physiol, 1991, 147, 311–318.[Medline]
Reiland J & Rapraeger AC. Heparan sulfate proteoglycan and FGF receptor target basic FGF to different intracellular destinations, J Cell Sci, 1993, 105, 1085–1093.[Abstract]
Riese J, Zeller R & Dono R. Nucleo-cytoplasmic translocation and secretion of fibroblast growth factor-2 during avian gastrulation, Mech Dev, 1995, 49, 13–22.[Medline]
Song J & Slack JMW. Spatial and temporal expression of basic fibroblast growth factor (FGF-2) mRNA and protein in early Xenopusdevelopment, Mech Dev, 1994, 48, 141–151.[Medline]
Stachowiak EK, Maher PA, Tucholski J, Mordechai E, Joy A, Moffett J, Coons S & Stachowiak MK. Nuclear accumulation of fibroblast growth factor receptors in human glial cells: association with cell proliferation, Oncogene, 1997, 14, 2201–2211.[Medline]
Stachowiak MK, Maher PA, Joy A, Mordechai E & Stachowiak EK. Nuclear localization of functional FGF receptor 1 in human astrocytes suggests a novel mechanism for growth factor action, Mol Brain Res, 1996a, 38, 161–165.[Medline]
Stachowiak MK, Maher PA, Joy A, Mordechai E & Stachowiak EK. Nuclear accumulation of fibroblast growth factor receptors is regulated by multiple signals in adrenal medullary cells, Mol Biol Cell, 1996b, 7, 1299–1317.[Abstract]
Stachowiak MK, Moffett J, Maher P, Tucholski J & Stachowiak EK. Growth factor regulation of cell growth and proliferation in the nervous system. A new intracrine nuclear mechanism, Mol Neurobiol, 1997, 15, 257–283.[Medline]
Steinfeld R, Van Den Berghe H & David G. Stimulation of fibroblast growth factor receptor-1 occupancy and signaling by cell surface-associated syndecans and glypican, J Cell Biol, 1996, 133, 405–416.
Umbhauer M, Marshall CJ, Mason CS, Old RW & Smith JC. Mesoderm induction in Xenopuscaused by activation of MAP kinase, Nature, 1995, 376, 58–62.[Medline]
Vagner S, Touriol C, Galy B, Audigier S, Gensac M-C, Amalric F, Bayard F, Prats H & Prats A-C. Translation of CUG- but not AUG-initiated forms of human fibroblast growth factor 2 is activated in transformed and stressed cells, J Cell Biol, 1996, 135, 1391–1402.
Webster MK & Donoghue DJ. Enhanced signaling and morphological transformation by a membrane-localized derivative of the fibroblast growth factor receptor 3 kinase domain, Mol Cell Biol, 1997, 17, 5739–5747.[Abstract]
Weinstein DC, Marden J, Carnevali F & Hemmati-Brivanlou A. FGF-mediated mesoderm induction involves the Src-family kinase Laloo, Nature, 1998, 394, 904–908.[Medline]
Wiedlocha A, Falnes PO, Madshus IH, Sandig K & Olsnes S. Dual mode of signal transduction by externally added acidic fibroblast growth factor, Cell, 1994, 76, 1039–1051.[Medline]
Wiedlocha A, Falnes PO, Rapak A, Munoz R, Klingenberg O & Olsnes S. Stimulation of proliferation of a human osteosarcoma cell line by exogenous acidic fibroblast growth factor requires both activation of receptor tyrosine kinase and growth factor internalization, Mol Cell Biol, 1996, 16, 270–280.[Abstract]
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