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  4. Transcription Factors STAT3 and MYC Are Key Players of Human Platelet Lysate-Induced Cell Proliferation

Transcription Factors STAT3 and MYC Are Key Players of Human Platelet Lysate-Induced Cell Proliferation

Int. J. Mol. Sci., 2022 · DOI: 10.3390/ijms232415782 · Published: December 13, 2022

Regenerative MedicineGenetics

Simple Explanation

Human platelet lysate (HPL) is a good substitute for animal serum and helps stromal cells grow a lot. This study looks at how HPL affects genes related to the cell cycle in human stromal cells. It also tries to find the key molecules that help HPL make cells grow faster. The study found that HPL makes cell cycle genes more active in stromal cells. Since HPL has lots of growth factors, the researchers used inhibitors that block tyrosine kinase receptor (TKR) pathways, which are activated by these growth factors, and they could slow down cell growth. The research shows that HPL boosts cell growth partly by increasing TKR signaling. This then increases the production of STAT3 and MYC, which in turn activate genes that control the cell cycle.

Study Duration
Not specified
Participants
Human bone marrow, umbilical cord and white adipose tissue stromal cells
Evidence Level
Not specified

Key Findings

  • 1
    HPL significantly affected cell cycle-specific protein expression compared to FBS-based culture, with more genes being upregulated than downregulated.
  • 2
    Blocking specific tyrosine kinase receptor (TKR) pathways lead to a significant reduction of HPL-induced cell proliferation.
  • 3
    STAT3 and MYC expression and activity seem to be elevated in HPL-based cell culture, and inhibiting STAT3 significantly decreased HPL-mediated proliferation of stromal cells.

Research Summary

This study investigates the effect of HPL on cell cycle gene expression in human stromal cells to identify key players mediating its growth-enhancing effects. The study found that HPL significantly affected cell cycle-specific protein expression, and blocking tyrosine kinase receptor pathways reduced HPL-induced cell proliferation. HPL-induced cell proliferation can be explained by enhanced TKR signaling, leading to elevated expression of STAT3 and MYC, which induce the expression of cell cycle promoting target genes.

Practical Implications

Clinical Propagation

HPL is a valuable alternative to FBS for clinical propagation of stromal cell-based medicinal applications.

Understanding Molecular Interactions

Findings contribute to understanding molecular interactions in HPL-based cell culture, particularly for therapeutic applications.

Therapeutic Application

The study sheds light on the molecular mechanisms behind the growth-promoting effect of HPL.

Study Limitations

  • 1
    The exact mechanisms of action of HPL are still not completely understood.
  • 2
    The phosphorylation status of p27 not determined, limiting conclusions.
  • 3
    Other pathways may contribute to mediate HPL’s growth-promoting effect as well.

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