Both Platelet-Derived Growth Factor Receptor (PDGFR)-α and PDGFR-β Promote Murine Fibroblast Cell Migration

2001 ◽  
Vol 282 (3) ◽  
pp. 697-700 ◽  
Author(s):  
Jiuhong Yu ◽  
Aree Moon ◽  
Hyeong-Reh Choi Kim
Keyword(s):  
Cell Migration ◽  
Growth Factor ◽  
Growth Factor Receptor ◽  
Fibroblast Cell ◽  
Platelet Derived Growth Factor ◽  
Murine Fibroblast

scholarly journals NHERF Links the N-Cadherin/Catenin Complex to the Platelet-derived Growth Factor Receptor to Modulate the Actin Cytoskeleton and Regulate Cell Motility

2007 ◽  
Vol 18 (4) ◽  
pp. 1220-1232 ◽  
Author(s):  
Christopher S. Theisen ◽  
James K. Wahl ◽  
Keith R. Johnson ◽  
Margaret J. Wheelock
Keyword(s):  
Cell Migration ◽  
Growth Factor ◽  
Kinase Inhibitor ◽  
Pdz Domain ◽  
Growth Factor Receptor ◽  
Cell Types ◽  
Platelet Derived Growth Factor ◽  
Binding Motif ◽  
Pdz Domains ◽  
Dependent Cell

Using phage display, we identified Na+/H+ exchanger regulatory factor (NHERF)-2 as a novel binding partner for the cadherin-associated protein, β-catenin. We showed that the second of two PSD-95/Dlg/ZO-1 (PDZ) domains of NHERF interacts with a PDZ-binding motif at the very carboxy terminus of β-catenin. N-cadherin expression has been shown to induce motility in a number of cell types. The first PDZ domain of NHERF is known to bind platelet-derived growth factor-receptor β (PDGF-Rβ), and the interaction of PDGF-Rβ with NHERF leads to enhanced cell spreading and motility. Here we show that β-catenin and N-cadherin are in a complex with NHERF and PDGF-Rβ at membrane ruffles in the highly invasive fibrosarcoma cell line HT1080. Using a stable short hairpin RNA system, we showed that HT1080 cells knocked down for either N-cadherin or NHERF had impaired ability to migrate into the wounded area in a scratch assay, similar to cells treated with a PDGF-R kinase inhibitor. Cells expressing a mutant NHERF that is unable to associate with β-catenin had increased stress fibers, reduced lamellipodia, and impaired cell migration. Using HeLa cells, which express little to no PDGF-R, we introduced PDGF-Rβ and showed that it coimmunoprecipitates with N-cadherin and that PDGF-dependent cell migration was reduced in these cells when we knocked-down expression of N-cadherin or NHERF. These studies implicate N-cadherin and β-catenin in cell migration via PDGF-R–mediated signaling through the scaffolding molecule NHERF.

The synergistic activity of alphavbeta3 integrin and PDGF receptor increases cell migration

1998 ◽  
Vol 111 (4) ◽  
pp. 469-478 ◽  
Author(s):  
A.S. Woodard ◽  
G. Garcia-Cardena ◽  
M. Leong ◽  
J.A. Madri ◽  
W.C. Sessa ◽  
...  
Keyword(s):  
Cell Migration ◽  
Growth Factor ◽  
Growth Factor Receptor ◽  
Platelet Derived Growth Factor ◽  
Microvascular Endothelial Cells ◽  
Synergistic Activity ◽  
3T3 Cells ◽  
Nih 3T3 ◽  
Receptor Beta ◽  
Nih 3T3 Cells

Integrins and growth factor receptors act synergistically to modulate cellular functions. The alphavbeta3 integrin and the platelet-derived growth factor receptor have both been shown to play a positive role in cell migration. We show here that a platelet derived growth factor-BB gradient stimulated migration of rat microvascular endothelial cells on vitronectin (9.2-fold increase compared to resting cells) in a alphavbeta3 and RGD-dependent manner. In contrast, this response was not observed on a beta1 integrin ligand, laminin; background levels of migration, in response to a platelet derived growth factor-BB gradient, were observed on this substrate or on bovine serum albumin (2.4- or 2.0-fold, respectively). Comparable results were obtained using NIH-3T3 cells. Platelet derived growth factor-BB did not change the cells' ability to adhere to vitronectin, nor did it stimulate a further increase in proliferation on vitronectin versus laminin. In addition, platelet derived growth factor-BB stimulation of NIH-3T3 cells did not alter the ability of alphavbeta3 to bind RGD immobilized on Sepharose. The alphavbeta3 integrin and the platelet derived growth factor receptor-beta associate in both microvascular endothelial cells and NIH-3T3 cells, since they coprecipitated using two different antibodies to either alphavbeta3 or to the platelet derived growth factor receptor-beta. In contrast, beta1 integrins did not coprecipitate with the platelet derived growth factor receptor-beta. These results point to a novel pathway, mediated by the synergistic activity of alphavbeta3 and the platelet derived growth factor receptor-beta, that regulates cell migration and, therefore, might play a role during neovessel formation and tissue infiltration.

scholarly journals Platelet-derived growth factor receptor-α is essential for cardiac fibroblast survival

2019 ◽  
Vol 317 (2) ◽  
pp. H330-H344 ◽  
Author(s):  
Malina J. Ivey ◽  
Jill T. Kuwabara ◽  
Kara L. Riggsbee ◽  
Michelle D. Tallquist
Keyword(s):  
Growth Factor ◽  
Cardiac Fibroblasts ◽  
Growth Factor Receptor ◽  
Fibroblast Cell ◽  
Cardiac Fibroblast ◽  
Platelet Derived Growth Factor ◽  
Activating Transcription Factor 3 ◽  
Rapid Reduction ◽  
Functional Changes

Platelet-derived growth factor receptor α (PDGFRα), a receptor tyrosine kinase required for cardiac fibroblast development, is uniquely expressed by fibroblasts in the adult heart. Despite the consensus that PDGFRα is expressed in adult cardiac fibroblasts, we know little about its function when these cells are at rest. Here, we demonstrate that loss of PDGFRα in cardiac fibroblasts resulted in a rapid reduction of resident fibroblasts. Furthermore, we observe that phosphatidylinositol 3-kinase signaling was required for PDGFRα-dependent fibroblast maintenance. Interestingly, this reduced number of fibroblasts was maintained long-term, suggesting that there is no homeostatic mechanism to monitor fibroblast numbers and restore hearts to wild-type levels. Although we did not observe any systolic functional changes in hearts with depleted fibroblasts, the basement membrane and microvasculature of these hearts were perturbed. Through in vitro analyses, we showed that PDGFRα signaling inhibition resulted in an increase in fibroblast cell death, and PDGFRα stimulation led to increased levels of the cell survival factor activating transcription factor 3. Our data reveal a unique role for PDGFRα signaling in fibroblast maintenance and illustrate that a 50% loss in cardiac fibroblasts does not result in lethality. NEW & NOTEWORTHY Platelet-derived growth factor receptor α (PDGFRα) is required in developing cardiac fibroblasts, but a functional role in adult, quiescent fibroblasts has not been identified. Here, we demonstrate that PDGFRα signaling is essential for cardiac fibroblast maintenance and that there are no homeostatic mechanisms to regulate fibroblast numbers in the heart. PDGFR signaling is generally considered mitogenic in fibroblasts, but these data suggest that this receptor may direct different cellular processes depending on the cell’s maturation and activation status.

Relative Platelet-derived Growth Factor Receptor Subunit Expression Determines Cell Migration to Different Dimeric Forms of PDGF

1990 ◽  
Vol 3 (4) ◽  
pp. 315-324 ◽  
Author(s):  
Gordon A. A. Ferns ◽  
Katherine H. Sprugel ◽  
Ronald A. Seifert ◽  
Daniel F. Bowen-Pope ◽  
James D. Kelly ◽  
...  
Keyword(s):  
Cell Migration ◽  
Growth Factor ◽  
Growth Factor Receptor ◽  
Platelet Derived Growth Factor ◽  
Receptor Subunit ◽  
Subunit Expression

scholarly journals Downregulation of platelet-derived growth factor receptor-β in Shp-2 mutant fibroblast cell lines

Oncogene ◽  
1998 ◽  
Vol 17 (4) ◽  
pp. 441-448 ◽  
Author(s):  
Xiaolan Lu ◽  
Cheng-Kui Qu ◽  
Zhong-Qing Shi ◽  
Gen-Sheng Feng
Keyword(s):  
Growth Factor ◽  
Cell Lines ◽  
Growth Factor Receptor ◽  
Fibroblast Cell ◽  
Platelet Derived Growth Factor ◽  
Fibroblast Cell Lines

scholarly journals Cell migration activated by platelet‐derived growth factor receptor is blocked by an inverse agonist of the sphingosine 1‐phosphate receptor‐1

2005 ◽  
Vol 20 (3) ◽  
pp. 509-511 ◽  
Author(s):  
Catherine M. Waters ◽  
Jaclyn Long ◽  
Irina Gorshkova ◽  
Yuko Fujiwara ◽  
Michelle Connell ◽  
...  
Keyword(s):  
Cell Migration ◽  
Growth Factor ◽  
Growth Factor Receptor ◽  
Inverse Agonist ◽  
Platelet Derived Growth Factor ◽  
Sphingosine 1 Phosphate
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