Pathway Map Details
Development_PDGF signaling via MAPK cascades
Object list (links open in MetaCore):
188.8.131.52, Ca('2+) endoplasmic reticulum lumen, Prostacyclin receptor, c-Jun, MEK1(MAP2K1), PDGF-C, IP3 receptor, PDGF-R-alpha, PKA-cat alpha, PKC-alpha, Ca('2) cytosol, ATP, Shc, H-Ras, PtdIns(3,4,5)P3, Elk-1, DAG, Adenylate cyclase type III, PDGF-D, PtdIns(4,5)P2, MEK4(MAP2K4), SRF, prostacyclin, PLC-gamma 1, PKC-epsilon, Rac1, PDGF-R-beta, PDGF-A, PKA-reg (cAMP-dependent), G-protein alpha-s, MEK2(MAP2K2), ERK1/2, 184.108.40.206, JNK(MAPK8-10), PDGF-B, cAMP, MEKK1(MAP3K1), SOS, 220.127.116.11, c-Raf-1, PDGF receptor,
PDGF signaling via MAPK cascades
Platelet-derived growth factors ( PDGF s) are members of a large family of growth factors secreted by human vascular endothelial cells and fibroblasts.
The PDGF family is composed of four different polypeptide chains encoded by four different genes. There are two classical PDGF chains, Platelet-derived growth factor alpha and beta polypeptides ( PDGF-A and PDGF-B), and two only recently discovered chains, Platelet derived growth factors C and D ( PDGF-C, PDGF-D ). The four PDGF chains assemble into homo- or heterodimers via disulphide bonds, and five different dimeric isoforms have been described so far; PDGF -AA, PDGF -AB, PDGF -BB, PDGF -CC and PDGF -DD.
PDGF s regulate biological functions in cells through binding to specific Platelet-derived growth factor receptor, alpha and beta polypeptides ( PDGF-R-alpha, PDGF-R-beta ) on the cell surface. The four dimeric isoforms, PDGF -AA, PDGF -AB, PDGF -BB and PDGF -CC can bind to and active PDGF-R-alpha, while PDGF -BB and PDGF -DD can specifically bind to and active PDGF-R-beta. PDGF -AB, PDGF -BB and PDGF -CC can also stimulate heterodimeric PDGF-R alpha/beta complexes .Upon ligand binding, PDGF-R-alpha and PDGF-R-beta dimerize and autophosphorylate on a number of tyrosine residues. Tyrosine phosphorylated sites are used by PDGF-receptor as anchor sites for various SH2 domain-containing proteins.
PDGF is a principal survival factor that inhibits apoptosis and promotes proliferation. The mechanisms of cell proliferation and transformation are intrinsically linked to the process of apoptosis: the default of proliferating cells is to undergo apoptosis unless specific survival signals are provided .
All types of PDGFs and PDGF-receptor may participate in proliferation of different cell types , , ,  via Mitogen-activated protein kinases 8-10 ( JNK(MAPK8-10) )  and Mitogen-activated protein kinase 1-3 ( ERK1/2 ) cascades .
PDGF-receptor directly activates the Phosphoinositide-3-kinase, regulatory ( PI3K reg class IA ) and the catalytic ( PI3K cat class IA ) subunits. PI3K reg class IA stimulates the activity of PI3K cat class IA, which in turn converts inositol 4,5-biphosphate ( PtdIns(4,5)P2 ) into inositol 3,4,5-trisphosphate ( PtdIns(3,4,5)P3 ). PtdIns(3,4,5)P3 stimulates Ras-related C3 botulinum toxin substrate 1 ( Rac1 ) through guanine nucleotide exchange factors (e.g., Vav 2 guanine nucleotide exchange factor ( VAV-2 )) .
Activated Rac1 stimulates Mitogen-activated protein kinase kinase kinase 1 ( MEKK1(MAP3K1) )/ Mitogen-activated protein kinase kinase 4 ( MEK4(MAP2K4) )/ JNK(MAPK8-10) pathway that leads to phosphorylation of the Jun oncogene ( c-Jun ) transcription factor. c-Jun induces activation of transcription of protein involved in cellular proliferation .
Sos may be recruited to the membrane by forming complexes with SHC (Src homology 2 domain containing) transforming protein 1 ( Shc )/ Grb2/ Sos or Grb2/ Sos. Activated Sos stimulates Harvey rat sarcoma viral oncogene homolog ( H-Ras ) by release of GDP . In turn, this leads to the activation ERK1/2 via v-raf-1 murine leukemia viral oncogene homolog 1 ( c-Raf-1 )/ Mitogen-activated protein kinase kinases 1 and 2 ( MEK1(MAP2K1) MEK2(MAP2K2) ) pathway. In addition, c-Raf-1 may be phosphorylated via PLC gamma 1 pathway and PDGF-receptor can activate PLC-gamma 1 by phosphorylation. Activation of PLC-gamma 1 leads to the hydrolysis of PtdIns(4,5)P2, generation of diacylglycerol ( DAG ) and inositol trisphosphate ( IP3 ) . DAG and IP3 stimulate Protein kinases C alpha and epsilon ( PKC-alpha, PKC- epsilon )   and mobilize intracellular Ca('2+), respectively. PKC s in turn phosphorylate c-Raf-1.
ERK1/2 cascade may be inhibited by prostacyclin. Prostacyclin (which can be synthesized after PDGF stimulation  ) binds to the Prostaglandin I2 (prostacyclin) receptor ( Prostacyclin receptor ), on the cell surface. Upon binding with prostacyclin, the receptor is stabilized in its active conformation and stimulates G-protein alpha-s. G-protein alpha-s acts as a signal transducers for activation of Adenylate cyclase 3 ( adenylate cyclase III ), which catalyzes the reaction of synthesis adenosine 3',5'-cyclic phosphate ( cAMP ) from adenosine-5'-triphosphate ( ATP ). The intracellular effects of cAMP in higher eukaryotes are primarily mediated by the activation of Protein kinase, cAMP-dependent, catalytic, alpha ( PKA-cat alpha ) .
Activated PKA-cat alpha phosphorylates v-raf-1 murine leukemia viral oncogene homolog 1 ( c-Raf-1 ) and blocks binding between v-Ha-ras Harvey rat sarcoma viral oncogene homolog ( H-Ras ) and c-Raf-1 and prevents participation c-Raf-1 in the activation of ERK1/2 signaling cascade .
Activation of the ERK1/2 cascade leads to phosphorylation of the ELK1, member of ETS oncogene family ( Elk-1), which stimulates serum response factor ( SRF ). SRF activates transcription some protein which participate in proliferation of cells .
In addition, it has been previously show, that Janus kinase 2 ( Jak2 )/ signal transducer and activator of transcription ( STAT ) pathway may participate in cellular proliferation by regulating the expression of immediate-early genes, such as proto-oncogene v-myc myelocytomatosis viral oncogene homolog ( c-Myc ) .
- Fredriksson L, Li H, Eriksson U
The PDGF family: four gene products form five dimeric isoforms. Cytokine & growth factor reviews 2004 Aug;15(4):197-204
- Romashkova JA, Makarov SS
NF-kappaB is a target of AKT in anti-apoptotic PDGF signalling. Nature 1999 Sep 2;401(6748):86-90
- Koyama N, Watanabe S, Tezuka M, Morisaki N, Saito Y, Yoshida S
Migratory and proliferative effect of platelet-derived growth factor in rabbit retinal endothelial cells: evidence of an autocrine pathway of platelet-derived growth factor. Journal of cellular physiology 1994 Jan;158(1):1-6
- Fruttiger M, Calver AR, Kruger WH, Mudhar HS, Michalovich D, Takakura N, Nishikawa S, Richardson WD
PDGF mediates a neuron-astrocyte interaction in the developing retina. Neuron 1996 Dec;17(6):1117-31
- Li X, Ponten A, Aase K, Karlsson L, Abramsson A, Uutela M, Backstrom G, Hellstrom M, Bostrom H, Li H, Soriano P, Betsholtz C, Heldin CH, Alitalo K, Ostman A, Eriksson U
PDGF-C is a new protease-activated ligand for the PDGF alpha-receptor. Nature cell biology 2000 May;2(5):302-9
- Ray S, Gao C, Wyatt K, Fariss RN, Bundek A, Zelenka P, Wistow G
Platelet-derived growth factor D, tissue-specific expression in the eye, and a key role in control of lens epithelial cell proliferation. The Journal of biological chemistry 2005 Mar 4;280(9):8494-502
- Mehrotra M, Krane SM, Walters K, Pilbeam C
Differential regulation of platelet-derived growth factor stimulated migration and proliferation in osteoblastic cells. Journal of cellular biochemistry 2004 Nov 1;93(4):741-52
- Monje P, Marinissen MJ, Gutkind JS
Phosphorylation of the carboxyl-terminal transactivation domain of c-Fos by extracellular signal-regulated kinase mediates the transcriptional activation of AP-1 and cellular transformation induced by platelet-derived growth factor. Molecular and cellular biology 2003 Oct;23(19):7030-43
- McKinnon RD, Waldron S, Kiel ME
PDGF alpha-receptor signal strength controls an RTK rheostat that integrates phosphoinositol 3'-kinase and phospholipase Cgamma pathways during oligodendrocyte maturation. The Journal of neuroscience : the official journal of the Society for Neuroscience 2005 Apr 6;25(14):3499-508
- Charvet C, Auberger P, Tartare-Deckert S, Bernard A, Deckert M
Vav1 couples T cell receptor to serum response factor-dependent transcription via a MEK-dependent pathway. The Journal of biological chemistry 2002 May 3;277(18):15376-84
- Jones SM, Kazlauskas A
Connecting signaling and cell cycle progression in growth factor-stimulated cells. Oncogene 2000 Nov 20;19(49):5558-67
- Rhee SG
Regulation of phosphoinositide-specific phospholipase C. Annual review of biochemistry 2001;70:281-312
- Ginnan R, Singer HA
PKC-delta-dependent pathways contribute to PDGF-stimulated ERK1/2 activation in vascular smooth muscle. American journal of physiology. Cell physiology. 2005 Jun;288(6):C1193-201
- Saito Y, Hojo Y, Tanimoto T, Abe J, Berk BC
Protein kinase C-alpha and protein kinase C-epsilon are required for Grb2-associated binder-1 tyrosine phosphorylation in response to platelet-derived growth factor. The Journal of biological chemistry 2002 Jun 28;277(26):23216-22
- Boulven I, Palmier B, Robin P, Vacher M, Harbon S, Leiber D
Platelet-derived growth factor stimulates phospholipase C-gamma 1, extracellular signal-regulated kinase, and arachidonic acid release in rat myometrial cells: contribution to cyclic 3',5'-adenosine monophosphate production and effect on cell proliferation. Biology of reproduction 2001 Aug;65(2):496-506
- Solberg R, Sandberg M, Natarajan V, Torjesen PA, Hansson V, Jahnsen T, Tasken K
The human gene for the regulatory subunit RI alpha of cyclic adenosine 3', 5'-monophosphate-dependent protein kinase: two distinct promoters provide differential regulation of alternately spliced messenger ribonucleic acids. Endocrinology 1997 Jan;138(1):169-81
- Dumaz N, Marais R
Protein kinase A blocks Raf-1 activity by stimulating 14-3-3 binding and blocking Raf-1 interaction with Ras. The Journal of biological chemistry 2003 Aug 8;278(32):29819-23
- Wang Z, Wang DZ, Hockemeyer D, McAnally J, Nordheim A, Olson EN
Myocardin and ternary complex factors compete for SRF to control smooth muscle gene expression. Nature 2004 Mar 11;428(6979):185-9
- Simon AR, Takahashi S, Severgnini M, Fanburg BL, Cochran BH
Role of the JAK-STAT pathway in PDGF-stimulated proliferation of human airway smooth muscle cells. American journal of physiology. Lung cellular and molecular physiology. 2002 Jun;282(6):L1296-304