PDPN

Case Study 1: Justyna Sikorska, 2019

Podoplanin (PDPN) is a mucin-type transmembrane glycoprotein specific to the lymphatic system. PDPN expression has been found in various human tumors and is considered to be a marker of cancer. The aim of this study was to determine the effect of PDPN down-regulation in another thyroid cancer-derived cell line: BcPAP.

The efficacy of PDPN silencing was confirmed by qRT-PCR and Western blotting. Then, the researchers tested the motility and invasiveness of these cells (using scratch test and Transwell assay), their growth capacities F(cell cycle analysis, viability, clonogenic activity) and apoptosis assays), adhesion-independent colony-formation capacities, as well as the effect of PDPN silencing on MMPs expression and activity (zymography). PDPN down-regulation in BcPAP cells was negatively correlated with the migration and invasion, in contrast to TPC1 cells in which PDPN depletion resulted in enhanced migration and invasiveness. They also demonstrated that PDPN expression is associated with the MAPK signaling pathway. The inhibition of the MAPK pathway resulted in a decreased PDPN expression, increased E/R/M phosphorylation and reduced cell migration.

Fig1. Immunofluorescent staining of podoplanin in BcPAP cells transfected with siPDPN or control siNeg.

Fig2. Western blot analysis of MMP expression levels 48 h after PDPN silencing.

Case Study 2: Satoshi Takagi, 2014

Platelet aggregation-inducing factor Aggrus, also known as podoplanin, is associated with tumor malignancy by promoting hematogenous metastasis. Aggrus overexpression has been reported in some tumor tissues including lung, esophagus, head and neck and brain. The researchers here found the frequent upregulation of aggrus mRNA in urinary bladder cancers using cancer tissue panels from various organs. Immunohistochemical analysis confirmed Aggrus protein expression in urinary bladder cancers and suggested a positive correlation between Aggrus expression and metastatic tendency in bladder cancers. Endogenous expression of Aggrus protein on the cell surface was found in the mouse bladder cancer MBT-2 cell line and human bladder cancer SCaBER cell lines. Knockdown of Aggrus expression in MBT-2 cells decreased their ability to induce platelet aggregation and form pulmonary metastasis in syngeneic mouse models. Knockdown of Aggrus expression in the human bladder cancer SCaBER cells also attenuated their ability to induce platelet aggregation and form pulmonary metastasis in mice. Moreover, pulmonary metastasis of SCaBER cells was prevented by prior administration of our generated anti-Aggrus neutralizing monoclonal antibodies by attenuating their retention in lung.

Fig3. Aliquots of cell lysates were immunoblotted with the anti-mouse Aggrus mAb.

Fig4. Aliquots of cell lysates were immunoblotted with the anti-human Aggrus mAb or anti-β-actin mAb.

PDPN involved in several pathways and played different roles in them. We selected most pathways PDPN participated on our site, such as GPVI-mediated activation cascade, Hemostasis, Platelet activation, signaling and aggregation, which may be useful for your reference. Also, other proteins which involved in the same pathway with PDPN were listed below. Creative BioMart supplied nearly all the proteins listed, you can search them on our site.

PDPN has several biochemical functions, for example, NOT amino acid transmembrane transporter activity, NOT folic acid transporter activity, NOT water channel activity. Some of the functions are cooperated with other proteins, some of the functions could acted by PDPN itself. We selected most functions PDPN had, and list some proteins which have the same functions with PDPN. You can find most of the proteins on our site.

PDPN has direct interactions with proteins and molecules. Those interactions were detected by several methods such as yeast two hybrid, co-IP, pull-down and so on. We selected proteins and molecules interacted with PDPN here. Most of them are supplied by our site. Hope this information will be useful for your research of PDPN.

TOM1L1

Research Area

Related articles