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Platelet-derived growth factor (PDGF) is a class of important growth factors primarily secreted by platelets, endothelial cells, and macrophages; it plays a pivotal role in various biological processes, including cell proliferation, migration, differentiation, and angiogenesis. It is not only essential for normal physiological processes—such as wound healing and tissue repair—but also plays a significant role in a variety of pathological conditions, including cancer, fibrosis, and atherosclerosis. The PDGF family comprises four distinct subtypes: PDGF-A, PDGF-B, PDGF-C, and PDGF-D. By binding to its receptors (PDGFRs), PDGF activates downstream signaling pathways, thereby regulating cellular behavior.

The Platelet-derived Growth Factor Receptor Beta (PDGFRB) is a cell-surface tyrosine kinase receptor belonging to the PDGF receptor family. Upon binding to its ligand, PDGF, PDGFRB undergoes dimerization and phosphorylation, thereby activating downstream signaling pathways—such as JAK-STAT3, PI3K-AKT-mTOR, and RAS-MAPK—and playing a critical role in regulating key cellular functions, including proliferation and apoptosis. Conversely, the aberrant activation of the PDGFRA protein can lead to tumorigenesis and promote tumor angiogenesis.

The HEK293 Human PDGF/PDGFRB Effector Reporter Cell Model—effectively simulates the signal transduction process of PDGFRB *in vivo*. The underlying principle is illustrated in the figure below.

Figure 1. Schematic Diagram of the HEK293 Human PDGF/PDGFRB Effector Reporter Cell Model

Figure 2. Recombinant PDGF/PDGFRB Effector Reporter Cell stably expressing PDGFRB.

Figure 3. Dose Response of Recombinant Human PDGF-BB in PDGF/PDGFRB Effector Reporter Cell(C26).

Figure 4. Inhibition of Human PDGF-BB-induced Reporter Activity by PDGFRB Blocking Abs in PDGF/DGFRB Effector Reporter Cell(C26). Inhibition of Human PDGF-BB-induced Reporter Activity by PDGFB Neutralization Ab in PDGF/PDGFRB Effector Reporter Cell(C26).

Cell Resuscitation
1)Rapidly thaw the frozen cells in a 37 °C water bath for approximately 60 seconds. Once thawed (which may take slightly less or more than 60 seconds), immediately transfer the cell suspension from the cryovial into a 15 mL centrifuge tube containing 10 mL of pre-warmed  HEK293 Human PDGF/PDGFRB Effector Reporter Cell complete culture medium.
2)Centrifuge cells at 1000 rpm for 5 min to remove medium, then resuspend cells in 5 mL of pre-warmed complete medium.
3)Transfer the cell suspension into a T25 culture flask and incubate at 37 °C with 5% CO₂.
4)After approximately 24–36 hours, replace the medium or passage the cells to remove non-adherent dead cells.

Subculturing procedure
1)When the cell density reaches the appropriate confluency for passaging, wash the cells with PBS, then add 1 mL trypsin to detach the cells. When more than 80% of the cells detach upon gently tapping the culture flask, add complete culture medium to terminate digestion. Gently pipette to obtain a single-cell suspension, transfer to a 15 mL centrifuge tube, and centrifuge at 1000 rpm for 5 minutes.

2)Discard supernatant after centrifugation. Resuspend cells in fresh medium to a single-cell suspension and transfer to a new culture flask for continued growth.

Cell Freezing
After trypsinization and centrifugation of cells from each T75 flask or 10 cm culture dish, discard the supernatant. Add 2 mL of cryopreservation medium (90% FBS + 10% DMSO), gently resuspend thoroughly, and aliquot into two cryovials. Immediately place the cryovials into a controlled-rate freezing container (e.g., Nalgene 5100-0001), fill with isopropanol to the indicated level, and store at −80 °C. After 24 hours, transfer the cryovials to liquid nitrogen for long-term storage.