Using Nanoparticles to Combat Arteriosclerosis

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On the left are fluorescence-labeled cells with nanoparticles: The cellular nuclei are shown in blue, the fluorescence labeling is shown in green and the nanoparticles in the cells are identified by arrows. The middle photo shows a blood vessel populated with these cells (green). On the right is a detailed image of a vascular wall with the eNOS protein identified (red). Credit: Dr. Sarah Rieck/Dr. Sarah Vosen/University of Bonn

On the left are fluorescence-labeled cells with nanoparticles: The cellular nuclei are shown in blue, the fluorescence labeling is shown in green and the nanoparticles in the cells are identified by arrows. The middle photo shows a blood vessel populated with these cells (green). On the right is a detailed image of a vascular wall with the eNOS protein identified (red). Credit: Dr. Sarah Rieck/Dr. Sarah Vosen/University of Bonn

A method for guiding replacement cells to diseased vascular segments using nanoparticles has been developed. Arteriosclerosis is common with fatal consequences. Deposits in the arteries lead to strokes and heart attacks. They demonstrated in mice that fresh cells actually exert their curative effect in these segments. However, much research remains to be done prior to use in humans.

In arterial calcification (arteriosclerosis), pathological deposits form in the arteries and this leads to vascular stenosis. Strokes and heart attacks are a frequent outcome due to the resultant insufficient blood flow. Endothelial cells which line the blood vessels play an important role here. “They produce nitric oxide and also regulate the expansion of the vessels and the blood pressure,” explains Jr Prof Dr. med. Daniela Wenzel. Damage to the endothelial cells is generally the insidious onset of arteriosclerosis.

His team developed a method with which damaged endothelial cells can regenerate and which they successfully tested in mice. The scientists transferred the gene for the enzyme eNOS into cultured cells with the aid of viruses. This enzyme timulates NO production in the endothelium like a turboloader. “The enzyme is an essential precondition for the full restoration of the original function of the endothelial cells,” reports Dr. Sarah Vosen from Jun.-Prof. Wenzel’s team.

Together with the gene, the scientists introduced tiny nanoparticles, measuring a few hundred nanometers with an iron core. “The iron changes the properties of the endothelial cells: They become magnetic,” explains Dr. Sarah Rieck. The nanoparticles ensure that the endothelial cells equipped with the ‘turbo’ gene can be delivered to the desired site in the blood vessel using a magnet where they exert their curative effect. Researchers at the Technische Universität München have developed a special ring-shaped magnet configuration for this which ensures that the replacement cells equipped with nanoparticles line the blood vessel evenly.

They tested this method in mice whose carotid artery endothelial cells were injured. They injected the replacement cells into the artery and were able to position them at the correct site using the magnet. “After half an hour, the endothelial cells adhered so securely to the vascular wall that they could no longer be flushed away by the bloodstream,” says Jun.-Prof. Wenzel. They then removed the magnets. As desired, the new endothelial cells produced nitric oxide and thus expanded the vessel, as is usual in the case of healthy arteries. “The mouse woke up from the anesthesia and ate and drank normally,” reported the physiologist.

Normally, doctors surgically remove vascular deposits from the carotid artery and in some cases place a stent to correct the bottleneck in the crucial blood supply. “However, these areas frequently become blocked with deposits once again,” reports Jun.-Prof. Wenzel. “In contrast, we are getting to the root of the problem and are restoring the original condition of healthy endothelial cells.” The researchers hope that what works in mice is also possible in humans, in principle. “There is still a considerable need for research.” http://www.alphagalileo.org/ViewItem.aspx?ItemId=159807&CultureCode=en