Artificial blood vessels mimic rare accelerated aging disease

Artificial blood vessels mimic rare accelerated aging disease
Progeria is a childhood disease with symptoms that resemble accelerated aging. Many affected patients die of heart disease brought on by weakened blood vessels before the age of 14. A single, random point mutation is responsible for the few hundred cases of progeria known in the world today. Credit: Progeria Research Foundation

Biomedical engineers have grown miniature human blood vessels that exhibit many of the symptoms and drug reactions associated with Hutchinson-Gilford Progeria Syndrome—an extremely rare genetic disease that causes symptoms resembling accelerated aging in children.

The technology will help doctors and researchers screen potential therapeutics for the disease more rapidly, with the goal of eventually creating a platform for personalized screening. The technique also offers a new way to study other rare diseases and could provide insights into treating in the elderly.

The study was published online on August 15 in the journal Scientific Reports.

"One of the drugs currently prescribed for this disease extends patients' lives by three months, and that's been considered a major feat," said Leigh Atchison, a doctoral candidate in at Duke University and first author of the study. "They're looking for anything that will extend lifespan by even a few months. It's that devastating."

Hutchinson-Gilford Progeria Syndrome—or simply for short—is a non-hereditary genetic disease caused by a single-point mutation in the genome. It is so rare and so deadly that there are currently only about 250 known cases worldwide.

Progeria is triggered by a defective protein called progerin that accumulates outside of a cell's nucleus rather than becoming part of its structural support system. This causes the nucleus to take on an abnormal shape and inhibits its ability to divide. The resulting symptoms look much like accelerated aging, and affected patients usually die of heart disease brought on by weakened blood vessels before the age of 14.

"Progeria isn't considered hereditary, because nobody lives long enough to pass it on," said George Truskey, the R. Eugene and Susie E. Goodson Professor of Biomedical Engineering at Duke. "There are currently 75 children in clinical trials, which is amazing given the rarity of the disease. But with 15 compounds under consideration for trials, the math just ultimately won't work out. You can't try all of these drugs or various combinations of them in humans, so we're hoping our platform will provide an alternative way to test them."

Blood vessels are difficult to simulate because their walls have multiple layers of , including the endothelium and the media. The endothelium is the innermost lining of all blood vessels that interacts with circulating blood. The media is made mostly of smooth muscle cells that help control the flow and pressure of the blood within.

Researchers believe that it is the deterioration of these smooth muscle cells that ultimately leads to the heart disease and failure that so often kills patients with progeria. But because there are so few people with progeria, it is extremely difficult to study in the patients themselves.

"Because it's such a hard disease to study, we wanted to see if we could create a platform using human cells that more accurately represents the disease and then use it for drug testing," said Atchison. "So we tried to grow miniature using induced derived from cells taken from patients with progeria."

The plan worked. In just four weeks of growth, the engineered blood vessels exhibit many of the symptoms seen in people with the disease—symptoms that simple cell cultures have not been able to recreate. The blood vessels also respond similarly to pharmaceuticals, revealing nuances into how current therapies are working.

While the vessels showed improved function after a week of being dosed with an analogue of rapamycin, a drug known as everolimus, calcification and other symptoms of cardiovascular disease remained. This implies that the drug is helping the smooth muscle cells work better, but not remedying the underlying symptoms.

"That's why our system could be so useful," said Atchison. "It could tell us exactly what the drug is doing in a quicker, more high-throughput manner, and whether we need a second treatment to address other aspects of the disease."

The success may aid the study of other , too.

"The major thing we're happy with is that this serves as a proof of principle for creating a vascular model of a rare disease in the laboratory to better understand it and hopefully develop a therapy," said Truskey.

The research may also provide insight into why some elderly people become especially prone to heart disease. Many heart patients have shown the same buildup of the progerin protein, so researchers believe there may be a link between the two conditions.

There are, of course, limitations to the new artificial . They are not connected to any outside organs, nor are they embedded in the complicated biology of a living human being.

"We only created from progeria patients in this study, but their endothelial cells might play a major role as well," said Atchison. "If we can incorporate derived from the patients' own cells into the model as well, then we can create a more personalized testing platform for these patients."


Explore further

Organ-on-a-chip model offers insights into premature aging and vascular disease

More information: Leigh Atchison et al, A Tissue Engineered Blood Vessel Model of Hutchinson-Gilford Progeria Syndrome Using Human iPSC-derived Smooth Muscle Cells, Scientific Reports (2017). DOI: 10.1038/s41598-017-08632-4
Journal information: Scientific Reports

Provided by Duke University
Citation: Artificial blood vessels mimic rare accelerated aging disease (2017, August 15) retrieved 9 December 2021 from https://medicalxpress.com/news/2017-08-artificial-blood-vessels-mimic-rare.html
This document is subject to copyright. Apart from any fair dealing for the purpose of private study or research, no part may be reproduced without the written permission. The content is provided for information purposes only.
40 shares

Feedback to editors