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Advanced application of porcine intramuscular adipocytes for evaluating anti-adipogenic and anti-inflammatory activities of immunobiotics.

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Academic year: 2017

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Fig 1. Photographic pictures of PIP and adipocyte cells. The PIP cells were grown at 37°C for 4 days, and subsequently fed with differentiation medium for another 4 days to differentiate into adipocyte cells
Fig 2. Expression of pattern of PPRs (TLR1 – 9, NOD 1, 2) and TNFR1, 2 in PIP, and differentiated adipocyte cells
Fig 3. TNF- α induced inflammatory cytokines in PIP and differentiated adipocyte cells
Fig 4. Expression of negative regulators in PIP and differentiated adipocyte cells. Both PIP cells and adipocytes were challenged with different concentrations of TNF-α (2.5, 25, and 250 ng/ml) for 24 hours and the level of negative regulators (MKP-1, A20,
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