For research use only
| Cat No. | ABC-TC3926 |
| Product Type | Mouse Primary Cells |
| Cell Type | Endothelial |
| Species | Mouse |
| Growth Conditions | 37 ℃, 5% CO2 |
| Source Organ | Liver |
| Disease | Normal |
| Storage | Liquid Nitrogen |
Mouse Hepatic Sinusoidal Endothelial Cells (MHSEC) are isolated from Swiss mice.
Mouse Hepatic Sinusoidal Endothelial Cells (HSECs) are primary cells isolated from the hepatic sinusoids of healthy mice. As the specialized endothelial cells lining hepatic sinusoids, they exhibit a flattened, cobblestone-like morphology and adherent growth pattern. Functionally, HSECs mediate nutrient exchange and maintain immune tolerance through phagocytic activity and cytokine secretion. Dysregulation of these cells is associated with liver fibrosis, cirrhosis, and inflammatory liver diseases. The cells express endothelial markers CD31 and VE-cadherin. HSECs have limited proliferative capacity in vitro. Each lot undergoes rigorous screening and isolation procedures, and is rigorously tested to ensure it is free of contamination from Mycoplasma, Fungi, Yeast, and Bacteria.
| Product Code | MHSEC |
| Species | Mouse |
| Cat.No | ABC-TC3926 |
| Product Category | Primary Cells |
| Size/Quantity | 1 vial |
| Cell Type | Endothelial |
| Growth Mode | Adherent |
| Shipping Info | Dry Ice |
| Growth Conditions | 37 ℃, 5% CO2 |
| Source Organ | Liver |
| Disease | Normal |
| Biosafety Level | 1 |
| Storage | Liquid Nitrogen |
| Product Type | Mouse Primary Cells |
| Quality Control | All cells test negative for mycoplasma, bacteria, yeast, and fungi. |
Mouse Hepatic Sinusoidal Endothelial Cells (HSECs) serve as a relevant in vitro cellular model for investigating the underlying mechanisms of liver and vascular disorders, such as non-alcoholic fatty liver disease (NAFLD), cirrhosis, and portal hypertension. These cells are particularly valuable for modeling the hepatic sinusoid unique microenvironment, allowing investigation of endothelial-stellate cell interactions, leukocyte trafficking, and responses to metabolic stressors like hyperlipidemia or insulin resistance. By recapitulating key aspects of sinusoidal dysfunction, HSECs provide a better understanding of their physiological roles in liver homeostasis and their pathological alterations in disease, supporting discovery research and molecular target identification for liver-related vascular and degenerative disorders.
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