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The Mastermind Behind Liver Fibrosis Revealed! Tame This Troublemaker for Flawless Experiments!​​

2025.09.14

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Groundbreaking Research Insights

Emerging evidence shows that stellate cell lactate transporter MCT1 significantly promotes liver fibrosis by increasing type I collagen expression in vitro and in vivo, while MCT1 silencing attenuates TGF-β1-stimulated collagen production in human LX2 stellate cells[3].


Similarly, inhibiting nucleophosmin (NPM) – highly expressed in fibrotic livers and activated HSCs – reduces fibrotic markers while suppressing HSC proliferation and migration. Genetic or proteomic NPM inhibition dramatically mitigates carbon tetrachloride-induced fibrogenesis in murine models[4].


Your Gateway to Fibrosis Breakthroughs

Targeting hepatic stellate cells (HSCs) represents a promising therapeutic strategy. Milecell Bio delivers premium primary HSCs engineered for research excellence:


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Primary isolation preserves in vivo activation traits, enabling precise modeling of fibrotic progression.


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Dual-gradient centrifugation + specific marker identification eliminates fibroblast contamination, ensuring data reliability.


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-196°C LN₂ flash-freezing guarantees ready-to-use convenience – faster than instant noodles!

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                                  SD HSC -D1                                                               BE HSC -D4                                                       CY HSC -D1

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                        BE-HSC                                                    SD-HSC                                                     CY-HSC


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LOTProductSpecification
CC57-HSCCryopreserved Mouse HSCs (Male, C57BL/6)0.5M
CCD-HSCCryopreserved Mouse HSCs (Male, CD-1)0.5M
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CBM-HSCCryopreserved Minipig HSCs (Male, Bama)0.5M


References

[1] Isaac, R. et al. (2024). Cell Metab 36(5):1030-1043. doi:10.1016/j.cmet.2024.04.003

[2] Aagaard, L. & Rossi, J.J. (2007). Adv Drug Deliv Rev 59(2-3):75-86. doi:10.1016/j.addr.2007.03.005

[3] Min, K. et al. (2024). eLife 12:RP89136. doi:10.7554/eLife.89136

[4] Ding, X. et al. (2023). Cell Death Dis 14(8):575. doi:10.1038/s41419-023-06043-0