Objectives:

The main objective of this study is to develop a method for in vitro T cell proliferation from rat peripheral blood mononuclear cells.

Materials and Methods:

The study involved female adult Albino Wistar rats, acclimatized for a week and used mononuclear cells for T cell enrichment. The cells were cultured in 24 and 6-Well Plates (WP) in the presence of PHA-M and analyzed for cytokines, cell counts, DNA content and morphology characteristics.

Key Facts:

MNCs were isolated and quantified, which revealed moderate to high variability across samples. The study found that TNF-α concentrations increased with the addition of PHA-M in DMEM and SFM 24-WP, with a peak at 20 μL. The 24-WP showed higher baseline and stimulated TNF-α levels compared to the 6-WP. The addition of PHA-M to DMEM 24-WP increases IFN-γ concentration, particularly at 10 μL, while it slightly decreases at 20 μL. In SFM 24-WP, it increases significantly at 20 μL. DMEM 24 WP 10 μL PHA-M has lower IL-6 concentrations, while DMEM 24 WP 20 μL PHA-M has the highest concentration. SFM 24 WP 20 μL PHA-M has significantly higher IL-6 levels. PHA-M stimulation significantly increased DNA concentration in DMEM 24 WP, with the highest concentration at 10 μL. PHA-M stimulation increased cell count, particularly with 10 μL, indicating successful proliferation. However, average cell size decreased with 10 μL of PHA-M for both media types.

Conclusion:

DMEM 24-WP at 10 μL of PHA-M offers a promising setup for experiments due to its balance between cytokine production and effective proliferation.