Human Adipose Microvascular Endothelial Cells (HAMEC)

Cat.No.: CSC-7846W

Species: Human

Source: Adipose

Cell Type: Endothelial Cell; Microvascular Cell

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Cat.No.
CSC-7846W
Description
Microvascular endothelial cells line blood vessels and contribute to many biological processes such as angiogenesis, coagulation, trafficking of lymphocytes, and the inflammatory response. Microvascular endothelial cells are diverse and have specific cellular characteristics and functions depending on the organ/tissue in which they are found. Adipose tissue is unique because it has the capacity to continually grow throughout adult life. It thus has a high occurrence of angiogenesis in order to provide the extensive vascularization require for adipose tissue. Studies have shown that angiogenesis precedes adipogenesis, implying that microvascular endothelial cells influence the proliferation of preadipocytes. Microvascular endothelial cell growth is at the same time stimulated by adipocyte secreted VEGG, suggesting a complex paracrine relationships between microvascular endothelial cells and preadipocytes during tissue development.HAMEC from Bioarray Research Laboratories are isolated from human adipose tissue. HAMEC are cryopreserved after purification and delivered frozen. Each vial contains >1 x 10^6 cells in 1 ml volume. HAMEC are characterized by immunofluorescent method with antibodies to vWF/Factor VIII and CD31 (P-CAM) and by uptake of DiI-Ac-LDL. HAMEC are negative for HIV-1, HBV, HCV, mycoplasma, bacteria, yeast and fungi. HAMEC are guaranteed to further expand for 15 population doublings at the conditions provided by Bioarray Research Laboratories.
Species
Human
Source
Adipose
Cell Type
Endothelial Cell; Microvascular Cell
Disease
Normal
Storage and Shipping
Directly and immediately transfer cells from dry ice to liquid nitrogen upon receiving and keep the cells in liquid nitrogen until cell culture needed for experiments.
Citation Guidance
If you use this products in your scientific publication, it should be cited in the publication as: Creative Bioarray cat no. If your paper has been published, please click here to submit the PubMed ID of your paper to get a coupon.

Human Adipose Microvascular Endothelial Cells (HAMVECs) are specialized endothelial cells isolated from the microvasculature of human adipose tissue. Given the critical role of adipose tissue as a dynamic endocrine organ, HAMVECs represent a physiologically relevant and high-impact model for studying the interplay between the vascular system, metabolic regulation, and tissue regeneration.

  • Tissue-Specific Metabolic Fidelity: Unlike generic macrovascular cells (e.g., HUVECs), HAMVECs retain the unique metabolic and signaling profile of the adipose microenvironment. This makes them the gold standard for research into obesity-related vascular dysfunction, insulin resistance, and type 2 diabetes.
  • Robust Angiogenic Potential: HAMVECs exhibit exceptional proliferation and tube-formation capabilities. They are highly responsive to pro-angiogenic factors (e.g., VEGF, bFGF), providing a superior platform for evaluating wound healing, tissue engineering, and anti-angiogenic drug candidates.
  • Inflammatory and Adhesion Dynamics: These cells are validated for the expression of key adhesion molecules (ICAM-1, VCAM-1, and E-selectin) and respond dynamically to inflammatory cytokines. They offer a precise model for studying leukocyte recruitment and chronic low-grade inflammation within the fat depot.
  • High Purity and Characterization: Our HAMVECs are strictly verified for endothelial markers including CD31 (PECAM-1), vWF, and DiI-Ac-LDL uptake, ensuring they are free from preadipocyte or fibroblast contamination for clean, reproducible experimental results.

By integrating HAMVECs into your research, you gain a human-derived, specialized tool that bridges the gap between systemic metabolic studies and cellular vascular biology.

Isolation of Primary HSaVEC, HITAEC, and HMVEC from Patients Undergoing Coronary Artery Bypass Graft Surgery

Primary human endothelial cells represent an essential tool to model endothelial dysfunction and to screen interventions for its treatment. Here, we developed a protocol for the synchronous isolation of primary human saphenous vein endothelial cells (HSaVEC), human internal thoracic artery endothelial cells (HITAEC), and human microvascular endothelial cells (HMVEC) from saphenous vein and internal thoracic artery utilized as conduits during coronary artery bypass graft surgery and from subcutaneous adipose tissue excised while providing an access to the heart. Treatment by collagenase type IV and magnetic separation with anti-CD31-antibody-coated beads ensured relatively high efficiency of the isolation (~60% for HSaVEC, ~50% for HITAEC, and ~20% for HMVEC) and high purity (≥99%) of isolated ECs within ~2 weeks (HSaVEC), ~2-3 weeks (HITAEC), and ~3-4 weeks (HMVEC). A colorimetric assay of cell viability and proliferation, as well as real-time bioimpedance monitoring demonstrated high proliferative activity in HSaVEC, HITAEC, and HMVEC, whilst the in vitro tube formation assay indicated their angiogenic potential. The isolation of HSaVEC, HITAEC, and HMVEC from patients undergoing coronary artery bypass graft surgery is a promising option to investigate endothelial heterogeneity, to interrogate endothelial responses to various stresses, and to pinpoint the optimal approaches for restoring endothelial homeostasis, thereby reproducing them within the bedside-to-bench-to-bedside concept.

Visualization and immunophenotyping of primary human adipose tissue-derived microvascular endothelial cells (HMVEC).

Fig. 1. Visualization (phase contrast microscopy, (left)) and immunophenotyping (flow cytometry, (right)) of primary human adipose tissue-derived microvascular endothelial cells (HMVEC) (Shishkova, Daria, et al., 2025).

Formation of capillary-like tubes by primary human saphenous vein endothelial cells (HSaVEC), human internal thoracic artery endothelial cells (HITAEC), and human adipose tissue-derived microvascular endothelial cells (HMVEC) after 24 h of culture in various endothelial cell media and in a three-dimensional gel matrix recapitulating the composition of the endothelial basement membrane.

Fig. 2. Formation of capillary-like tubes by HSaVEC, HITAEC, and HMVEC after 24 h of culture in various endothelial cell media and in a three-dimensional gel matrix recapitulating the composition of the endothelial basement membrane (Shishkova, Daria, et al., 2025).
What are the benefits of Human Adipose Microvascular Endothelial Cells (HAMEC)?

Studies have shown that angiogenesis precedes adipogenesis, implying that microvascular endothelial cells influence the proliferation of preadipocytes. At the same time, microvascular endothelial cell growth is stimulated by adipocyte secreted VEGG, suggesting a complex paracrine relationship between microvascular endothelial cells and preadipocytes during tissue development.

What passage number would they be?

You will receive Human Adipose Microvascular Endothelial Cells (HAMEC) at passages 2 or 3, depending on cell purity.

Is there a recommended medium?

It is recommended to use SuperCult® Custom-Made Endothelial Cell Medium (cat# CM-1085X) for the culturing of HAMEC.

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Average Rating: 5.0    |    1 Scientist has reviewed this product

Excellent reproducibility

The cell product has excellent reproducibility.

18 May 2022


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