4.2 Article

Commercial human pulmonary artery endothelial cells have in-vitro behavior that varies by sex

Journal

PULMONARY CIRCULATION
Volume 12, Issue 4, Pages -

Publisher

WILEY
DOI: 10.1002/pul2.12165

Keywords

cultured; endothelial cells; humans; in vitro techniques; sex characteristics

Funding

  1. National Heart, Lung, and Blood Institute [5P20GM103652, R01-HL141268, T32-HL134625]

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This study investigates the possible influence of biological sex on the behavior of commercially available human pulmonary artery endothelial cells (HPAECs). The results suggest that there are subtle sex-based differences in HPAECs' behavior, which depend on the sex and age of the donors. Female cells show decreased proliferation and increased apoptosis compared to male cells, but exhibit stronger migration under certain conditions. These differences may affect the reliability and reproducibility of experiments, and further research is needed to determine the importance of biological sex in HPAECs' function in health and disease.
It is unknown whether biological sex influences phenotypes of commercially available human pulmonary artery endothelial cells (HPAECs). Ten lots of commercial HPAECs were used (Lonza Biologics; PromoCell). Five (50%) were confirmed to be genotypically male (SRY+) and five (50%) were confirmed to be female (SRY-). Experiments were conducted between passages five and eight. HPAEC phenotype was confirmed with a panel of cell expression markers. Standard assays for proliferation, migration and tube formation were performed in triplicate with technical replicates, under three treatment conditions (EndoGRO; Sigma-Aldrich). Apoptosis was assessed by exposing cells treated with complete media or low serum media to hypoxic (1% oxygen) or normoxic (20% oxygen) conditions. Laboratory staff was blinded. The median (range) age of male and female donors from whom the HPAECs were derived was 58 (48-60) and 56 (33-67), respectively. Our results suggest decreased proliferation in genotypically female cells compared with male cells (p = 0.09). With increasing donor age, female cells were less proliferative and male cells were more proliferative (p = 0.001). Female cells were significantly more apoptotic than male cells by condition (p = 0.001). Female cells were significantly more migratory than male cells in complete media but less migratory than male cells under vascular endothelial growth factor enriched conditions (p = 0.001). There are subtle sex-based differences in the behavior of HPAECs that depend on donor sex and, less so, age. These differences may undermine rigor and reproducibility. Future studies should define whether biological sex is an important regulator of HPAEC function in health and disease.

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