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Updated: Jun 16, 2026

A Simple Bioassay for the Evaluation of Vascular Endothelial Growth Factors
Published on: March 15, 2016
Cardiac microvascular endothelial cells express and release nerve growth factor but not fibroblast growth factor-2
Shimon Lecht1, Carola Foerster, Hadar Arien-Zakay
1The School of Pharmacy Institute for Drug Research, Faculty of Medicine, The Hebrew University of Jerusalem, Jerusalem, 91120, Israel.
Insights
Endothelial cells (ECs) in the heart and brain show distinct neuro-angiogenic factor secretion. Brain ECs release FGF-2, while both release NGF, with secretion impacted by ischemic conditions.
Area of Science:
- Vascular Biology
- Neuroscience
- Cellular Physiology
Background:
- Endothelial cells (ECs) exhibit heterogeneity across vascular beds.
- This heterogeneity influences their distinct physiological roles.
- Differential expression of neuro-angiogenic factors contributes to EC function.
Purpose of the Study:
- To investigate gene expression and secretion of neuro-angiogenic factors (NGF, FGF-2) by myocardial and cerebral ECs.
- To assess the impact of oxygen-glucose deprivation on these factors.
- To understand the role of EC heterogeneity in tissue homeostasis.
Main Methods:
- RT-PCR for gene expression analysis.
- PC12 bioassay for neurotropic activity.
- ELISAs for NGF and FGF-2 quantification in conditioned media.
- Culture of ECs from myocardial and cerebral capillaries.
Main Results:
- NGF was expressed and released by both heart and brain ECs.
- FGF-2 was exclusively expressed and released by brain ECs.
- Ischemic insult blocked NGF secretion from both EC types and reduced brain EC FGF-2 secretion by 70%.
Conclusions:
- Differential expression of NGF and FGF-2 highlights EC heterogeneity.
- This heterogeneity is crucial for tissue-specific homeostasis.
- Microenvironmental factors, like ischemia, significantly modulate EC factor secretion.
Abstract:
Endothelial cells (ECs) from different vascular beds not only display common characteristics but are also quite heterogeneous in terms of expression and secretion of neuro-angiogenic factors, which may help explain some of their distinct physiological roles. We investigated by RT-PCR the gene expression, by PC12 bioassay the neurotropic activity, and by ELISAs the levels of NGF and FGF-2 using conditioned medium collected from cultures of ECs derived from myocardial and cerebral capillaries. While NGF was expressed and released by both cell types, FGF-2 was expressed and released solely by the brain but not heart ECs. Oxygen-glucose deprivation (ischemic) insult blocked NGF secretion from heart and brain ECs and inhibited by 70% the secretion of FGF-2 from brain ECs. We propose that the differential expression of NGF and FGF-2 in heart and brain EC cultures reflect heterogeneity on demand of the microcapillary components and the surrounding microenvironment for a proper tissue-specific homeostasis.
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