Chinese scientists find genetic switch for organ regeneration in mammals
Breakthrough in regenerative medicine from Chinese researchers at NIBS and BGI Research. Publication in Science showed how to restore healing ability in mammals.
The key is the Aldh1a2 gene, responsible for vitamin A metabolism. In fish and salamanders, it is active, but in mammals, it is blocked by evolution.
Scientists "switched on" this gene in mice and rats, leading to complete regeneration of soft and joint tissues. The mechanism works through the production of retinoic acid.
This discovery could simplify the treatment of bone, limb, skin, nerve, and lung injuries in humans.
#regeneration #Aldh1a2 #biotechnology #China #Science
Breakthrough in regenerative medicine from Chinese researchers at NIBS and BGI Research. Publication in Science showed how to restore healing ability in mammals.
The key is the Aldh1a2 gene, responsible for vitamin A metabolism. In fish and salamanders, it is active, but in mammals, it is blocked by evolution.
Scientists "switched on" this gene in mice and rats, leading to complete regeneration of soft and joint tissues. The mechanism works through the production of retinoic acid.
This discovery could simplify the treatment of bone, limb, skin, nerve, and lung injuries in humans.
#regeneration #Aldh1a2 #biotechnology #China #Science
english.news.cn
Chinese scientists discover genetic switch for organ regeneration in mammals
BEIJING, June 27 (Xinhua) -- Chinese scientists have achieved a major breakthrough in regenerative medicine by identifying a genetic switch that can restore healing abilities in mammals, a discovery that could revolutionize treatments for organ damage and…
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🧬 Cambridge Scientists Reverse "Irreversible" Nerve Damage in Lab-Grown Human Brain-Spinal Cord Model
Researchers at the University of Cambridge have built a miniature human brain-spinal cord system in the lab and used it to overturn a long-held assumption: that nerve damage in the central nervous system is permanent.
The team, led by Dr. András Lakatos, grew pea-sized brain and spinal cord organoids from human stem cells and kept them physically separate. Axons from the brain tissue grew across the gap and connected with the spinal cord tissue, forming a functional neural circuit that could even trigger muscle contractions.
Key findings:
— Neurons could regrow damaged axons until roughly day 150 of development (mid-pregnancy equivalent). After that, a sharp decline in regenerative ability sets in — a biological switch hardwired into maturing human neurons.
— The team identified the gene network responsible for this switch. When they blocked its key regulators, neurons regained the ability to grow axons again.
— An existing drug, lynestrenol (a hormone currently approved for menstrual disorders), significantly improved axon regrowth when tested on the damaged neurons.
— While lynestrenol itself is unlikely to be the clinical answer, it proves the principle: human neurons can be directly targeted to regenerate.
Quote from Dr. Lakatos: "When the brain and spinal cord are damaged, the nerve fibers that carry movement signals rarely grow back. That's why paralysis is usually permanent. But our model shows this block can be reversed."
This matters because most nerve regeneration research has relied on rodents, whose neurons behave differently from human ones. Human organoid models bridge that gap and may accelerate the path to treating conditions like spinal cord injury, motor neurone disease, and multiple sclerosis.
Original paper (Cell Reports): https://www.cell.com/cell-reports/fulltext/S2211-1247(26)00477-8
ScienceDaily summary: https://www.sciencedaily.com/releases/2026/05/260528082459.htm
#neuroscience #organoids #regeneration #spinalcordinjury #cambridge
Researchers at the University of Cambridge have built a miniature human brain-spinal cord system in the lab and used it to overturn a long-held assumption: that nerve damage in the central nervous system is permanent.
The team, led by Dr. András Lakatos, grew pea-sized brain and spinal cord organoids from human stem cells and kept them physically separate. Axons from the brain tissue grew across the gap and connected with the spinal cord tissue, forming a functional neural circuit that could even trigger muscle contractions.
Key findings:
— Neurons could regrow damaged axons until roughly day 150 of development (mid-pregnancy equivalent). After that, a sharp decline in regenerative ability sets in — a biological switch hardwired into maturing human neurons.
— The team identified the gene network responsible for this switch. When they blocked its key regulators, neurons regained the ability to grow axons again.
— An existing drug, lynestrenol (a hormone currently approved for menstrual disorders), significantly improved axon regrowth when tested on the damaged neurons.
— While lynestrenol itself is unlikely to be the clinical answer, it proves the principle: human neurons can be directly targeted to regenerate.
Quote from Dr. Lakatos: "When the brain and spinal cord are damaged, the nerve fibers that carry movement signals rarely grow back. That's why paralysis is usually permanent. But our model shows this block can be reversed."
This matters because most nerve regeneration research has relied on rodents, whose neurons behave differently from human ones. Human organoid models bridge that gap and may accelerate the path to treating conditions like spinal cord injury, motor neurone disease, and multiple sclerosis.
Original paper (Cell Reports): https://www.cell.com/cell-reports/fulltext/S2211-1247(26)00477-8
ScienceDaily summary: https://www.sciencedaily.com/releases/2026/05/260528082459.htm
#neuroscience #organoids #regeneration #spinalcordinjury #cambridge
Cell Reports
A human corticospinal organoid-slice connectoid model informs enhancer strategies for post-injury axon regrowth
Gibbons et al. present a human corticospinal organoid slice-based connectoid model,
with physically separate but functionally coupled cortical and spinal regions. Allowing
cell-type-specific observations, the platform uncovers a developmental maturation-dependent…
with physically separate but functionally coupled cortical and spinal regions. Allowing
cell-type-specific observations, the platform uncovers a developmental maturation-dependent…
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