While watching these fish repair their own spinal cord
injuries, Duke University scientists have found a particular protein
important for the process. Their study, published Nov. 4 in the journal Science, could generate new leads into tissue repair in humans.
"This is one of nature's most remarkable feats of regeneration," said
the study's senior investigator Kenneth Poss, professor of cell biology
and director of the Regeneration Next initiative at Duke. "Given the
limited number of successful therapies available today for repairing
lost tissues, we need to look to animals like zebrafish for new clues
about how to stimulate regeneration."
When the zebrafish's severed spinal cord undergoes regeneration, a
bridge forms, literally. The first cells extend projections into a
distance tens of times their own length and connect across a wide gulf
of the injury. Nerve cells follow. By 8 weeks, new nerve tissue has
filled the gap and the animals have fully reversed their severe
paralysis.
To understand what molecules were potentially responsible for this
remarkable process, the scientists conducted a molecular fishing
expedition of sorts, searching for all of the genes whose activity
abruptly changed after spinal cord injury.
Of dozens of genes strongly activated by injury, seven coded for
proteins that are secreted from cells. One of these, called CTGF or
connective tissue growth factor, was intriguing because its levels rose
in the supporting cells, or glia, that formed the bridge in the first
two weeks following injury.
"We were surprised that it was expressed in only a fraction of glial cells after the injury. We thought that these glial cells
and this gene must be important," said lead author Mayssa Mokalled, a
postdoctoral fellow in Poss's group. Indeed, when they tried deleting
CTGF genetically, those fish failed to regenerate.
Humans and zebrafish share most protein-coding genes, and CTGF is no
exception. The human CTGF protein is nearly 90% similar in its amino
acid building blocks to the zebrafish form. When the team added the
human version of CTGF to the injury site in fish, it boosted
regeneration and the fish swam better by two weeks after the injury.
"The fish go from paralyzed to swimming in the tank. The effect of the protein is striking," Mokalled said.
The second half of the CTGF protein seems to be the key to the
healing, the group found. It's a large protein, made of four smaller
parts, and it has more than one function. That might make it easier to
deliver and more specific as a therapy for spinal injuries.
Poss said that unfortunately, CTGF is probably not sufficient on its
own for people to regenerate their own spinal cords. Healing is more
complex in mammals, in part because scar tissue forms around the injury.
Poss's group expects studies of CTGF to move into mammals like mice.
"Mouse experiments could be key," Mokalled said. "When do they express CTGF, and in what cell types?"
These experiments may reveal some answers to why zebrafish can
regenerate whereas mammals cannot. It may be a matter of how the protein
is controlled rather than its make-up, Poss said.
The group also plans to follow up on other proteins secreted after
injury that were identified in their initial search, which may provide
additional hints into the zebrafish's secrets of regeneration.
"I don't think CTGF is the complete answer, but it's a great thing to
have in hand to inform new ways to think about the real challenge of
trying to improve regeneration," Poss said.
Other scientists involved in the study were Amy Dickson and Toyokazu
Endo, also at Duke University, and Chinmoy Patra and Didier Stainier at
the Max Planck Institute for Heart and Lung Research.
SOURCE:
MedicalXpress and Provided by:
Duke University




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