Building blocks of blood vessels, known as pericytes, have been linked to inflammation and disease processes in male mice.
A study conducted by York University sheds new light on the biological differences between male and female mice when it comes to obesity-related diseases. The research reveals “striking” disparities in the cells that construct blood vessels in the fatty tissue of male compared to female mice.
According to Professor Tara Haas of the Faculty of Health’s School of Kinesiology and Health Science at York University, men have a higher likelihood of developing obesity-related conditions like cardiovascular disease, insulin resistance, and diabetes compared to women.
“People have used rodent models to study obesity, and the diseases that are associated with obesity — like diabetes — but they’ve typically always studied male rodents because females are resistant to developing the same kinds of diseases,” says Haas, lead on the study. “We were really interested in exploring that difference because, to us, it spoke of something really fascinating happening in females that protects them.”
Haas and her team observed in an earlier study that when mice become obese, females grow a lot of new blood vessels to supply the expanding fat tissue with oxygen and nutrients, whereas males grow a lot less. In this latest study published in iScience, Haas and her co-authors, including York Ph.D. student Alexandra Pislaru, Faculty of Health Assistant Professor Emilie Roudier, and former York post-doctorate student Martina Rudnicki, focused on differences in the endothelial cells that make up the building blocks of these blood vessels in fat tissue.
A video of professor Tara Haas and Alexandra Pislaru explaining the study. Credit: York University
The team used software to help sift through thousands of genes to zero in on the ones that would be associated with blood vessel growth. They discovered that processes associated with the proliferation of new blood vessels were high in the female mice, whereas the males had a high level of processes associated with inflammation.
“It was very striking the extent of inflammation-associated processes that were prevalent in the males,” Haas recalls. “Other studies have shown that when endothelial cells have that kind of inflammatory response, they’re very dysfunctional, and they don’t respond to stimuli properly.”
Pislaru, who works in Haas’ lab and is a co-first author of the study, participated in this project as part of her dissertation.
“It is exciting to observe the continuing resilience that female endothelial cells display even when stressed by a long-term high-fat diet,” Pislaru says. “The findings from our study can help researchers to get a better understanding of why obesity manifests differently in men and women.”
The researchers also examined the behavior of the endothelial cells when they were taken out of the body and studied in Petri dishes.
“Even when we take them out of the body where they don’t have the circulating sex hormones or other kinds of factors, male and female endothelial cells still behave very differently from each other,” Haas explains.
Female endothelial cells replicated faster, while male endothelial cells displayed greater sensitivity to an inflammatory stimulus. By comparing with previously published data sets, the researchers found endothelial cells from aged male mice also displayed a more inflammatory profile compared to female cells.
“You can’t make the assumption that both sexes are going to respond to the same series of events the same way,” says Haas. “This isn’t just an obesity-related issue — I think it’s a much broader conceptual problem that also encompasses healthy aging. One implication of our findings is that there will be situations where the treatment that is ideal for men is not going to be ideal for women and vice-versa.”
While humans and mice have different genes that may be turned up or down, Haas believes the general findings would likely apply and is interested in studying the same cells in humans in future research.
Reference: “Transcriptomic profiling reveals sex-specific molecular signatures of adipose endothelial cells under obesogenic conditions” by Martina Rudnicki, Alexandra Pislaru, Omid Rezvan, Eric Rullman, Aly Fawzy, Emmanuel Nwadozi, Emilie Roudier, Thomas Gustafsson and Tara L. Haas, 16 December 2022, iScience.
The study was funded by a grant through the Canadian Institutes of Health Research, as well as the Natural Science and Engineering Research Council of Canada and York’s Faculty of Health.