This microscope image shows a colony of neurons derived from
cord-blood cells using stem cell reprogramming technology.
The green and red glow indicates that the cells are producing protein markers found
in neurons, evidence that the cord-blood cells did in fact morph into neurons.
The blue glow marks the nuclei of the neurons.
Image: Courtesy of Alessandra Giorgetti
Neurons Made from Cord Blood May Open New Neurologic Therapies
For more than 20 years, doctors have been using cells from blood in the placenta and umbilical cord after childbirth to treat a variety of illnesses, from cancer and immune disorders to blood and metabolic diseases. Now using transcription factor to convert Cord Blood cells into neurons, opens the way for treatment of neruologic conditions
Scientists at the Salk Institute for Biological Studies have found a new way of using a single protein, known as a transcription factor, to convert cord blood (CB) cells into neuron-like cells that may prove valuable for the treatment of a wide range of neurological conditions, including stroke, traumatic brain injury and spinal cord injury.
The researchers demonstrated that these CB cells,
which come from the mesoderm,
the middle layer of embryonic germ cells,
can be switched to ectodermal cells,
outer layer cells from which
brain, spinal and nerve cells arise.
"This study shows for the first time the direct conversion of a pure population of human cord blood cells into cells of neuronal lineage by the forced expression of a single transcription factor," says Juan Carlos Izpisua Belmonte, a professor in Salk's Gene Expression Laboratory, who led the research team.
The study, a collaboration with Fred H. Gage, a professor in Salk's Laboratory of Genetics, and his team, was published on July 16 in the Proceedings of the National Academy of Sciences.
"Unlike previous studies, where multiple transcription factors were necessary to convert skin cells into neurons, our method requires only one transcription factor to convert CB cells into functional neurons," says Gage.
The Salk researchers used a retrovirus to introduce Sox2,
a transcription factor that acts as a switch in neuron
development, into CB cells.
After culturing them in the laboratory, they discovered colonies of cells expressing neuronal markers. Using a variety of tests, they determined that the new cells, called induced neuronal-like cells (iNC), could transmit electrical impulses, signaling that the cells were mature and functional neurons.
Additionally, they transferred the Sox2-infused CB cells to a mouse brain and found that they integrated into the existing mouse neuronal network and were capable of transmitting electrical signals like mature functional neurons.
"We also show that the CB-derived neuronal cells can be expanded under certain conditions and still retain the ability to differentiate into more mature neurons both in the lab and in a mouse brain," says Mo Li, a scientist in Belmonte's lab and a co-first author on the paper with Alessandra Giorgetti, of the Center for Regenerative Medicine, in Barcelona, and Carol Marchetto of Gage's lab.
Li: "Although the cells we developed were not for a specific lineage-for example, motor neurons or mid-brain neurons-we hope to generate clinically relevant neuronal subtypes in the future."
Importantly, says Marchetto, "We could use these cells in the future for modeling neurological diseases such as autism, schizophrenia, Parkinson's or Alzheimer's disease."
Cord blood cells, says Alessandra Giorgetti, offer a number of advantages over other types of stem cells:
• they are not embryonic stem cells, thus not controversial.
• they are more plastic, or flexible, than adult stem cells
• collection is safe, painless, posing no risk to the donor
• CB cells can be stored in blood banks for later use.
Li: "If our protocol is developed into a clinical application, it could aid in future cell-replacement therapies. You could search all the cord blood banks in the country to look for a suitable match."
Other researchers on the study were Diana Yu, Yangling Mu, Cedric Bardy and Guang-Hui Liu, from the Salk Institute; and Rafaella Fazzina, Antonio Adamo, Ida Paramonov, Julio Castaño Cardoso, Montserrat Barragan Monasterio and Riccardo Cassiani-Ingoni of the Center for Regenerative Medicine in Barcelona.
The work was supported by the California Institute for Regenerative Medicine, The Lookout Foundation, the G. Harold and Leila Y. Mathers Charitable Foundation, the Leona M. and Harry B. Helmsley Charitable Trust, the JPB Medical Foundation, MINECO, Fundacion Cellex and Sanofi.
About the Salk Institute for Biological Studies:
The Salk Institute for Biological Studies is one of the world's preeminent basic research institutions, where internationally renowned faculty probe fundamental life science questions in a unique, collaborative, and creative environment. Focused both on discovery and on mentoring future generations of researchers, Salk scientists make groundbreaking contributions to our understanding of cancer, aging, Alzheimer's, diabetes and infectious diseases by studying neuroscience, genetics, cell and plant biology, and related disciplines.
Faculty achievements have been recognized with numerous honors, including Nobel Prizes and memberships in the National Academy of Sciences. Founded in 1960 by polio vaccine pioneer Jonas Salk, M.D., the Institute is an independent nonprofit organization and architectural landmark.
Original article: http://www.salk.edu/news/pressrelease_details.php?press_id=571