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Nanoparticles + Stem Cells = Faster Healing Wounds

80beatsBy Brett IsraelOctober 8, 2009 2:48 AM


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While stem cells can rapidly grow into any kind of new tissue, they aren't always able to encourage new blood vessels to grow so that the tissue stays alive.


A new study may have hit upon another way to improve stem cells' ability to help repair damaged tissue.

But in a new study, published in the Proceedings of the National Academy of Sciences, scientists describe a way around the problem.

The researchers used nanoparticles to ferry a key gene into the stem cells, which caused the cells to recruit new blood vessels, thus fueling tissue growth.

The nanoparticles carried a gene (VEGF) that is known to stimulate new blood vessel growth. When the modified cells were injected into mice whose hind limbs had been injured, the tissue that regrew to repair the damage had three times the blood vessel density of similar tissue in mice given unmodified cells. Four weeks later, only 20 per cent of the mice given modified cells had lost limbs, compared with 60 per cent in mice that received unmodified cells [New Scientist].

The researchers are optimistic about the nanoparticle approach, however they state in the study that the effect may be transient. They note that

there was a significant increase in VEGF levels in mouse muscle two days following cell grafting, but VEGF levels produced by the cells dropped sharply after four days [The Scientist]. They say that using a virus to transmit the gene may be a better approach to stimulate new blood vessels over a longer period of time. However, the viral approach is not without risks--viruses can

integrate into the genome of cells and linger permanently, potentially causing cancer or immune reactions [Bloomberg].

Related Content: 80beats: A Safer Way to Transform Skin Cells Into Stem Cells Brings Medical Trials Closer 80beats: Biotech Co: First Human Embryonic Stem Cell Trial Hit Small Speed Bump 80beats: Adult Mouse Gets a New Tooth, Grown From Embryonic CellsImage: iStockphoto

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