His relationship with PTEN took an entirely new direction recently, when his team at CSHL and collaborators led by Dr. Seong-Seng Tan at聽the Florey Neuroscience Institutes in Australia discovered a new role for the PTEN protein in the brain, one that could potentially be exploited in designing a therapy for stroke.
When a stroke cuts off blood supply to a brain region, the neurons in that region are in danger of perishing due to the resulting drop in the levels of oxygen and essential nutrients. Trotman and the other researchers have discovered how modulation of PTEN function, via a change in the protein鈥檚 cellular location within neurons, aids their survival in this situation.
Trotman鈥檚 collaborators were interested in understanding the genetics of stroke and finding genes that are important in repairing damage and boosting neuronal survival. While investigating genetic activity within the affected brain areas of mice that had undergone stroke, the team found two genes that seem to be regulated by ischemia鈥攖he loss in blood supply that causes stroke.
One of these genes is Ndfip1, which encodes a protein that facilitates protein transport鈥攁 process that moves proteins from one cellular compartment to another. The other gene encodes a protein called Nedd4, which modifies other proteins in a way that usually targets them for destruction.
鈥淭hat鈥檚 when we came into the picture,鈥� says Trotman. His team had previously found that Nedd4 interacts with PTEN within cells. This discovery was surprising because the interaction did not result in the destruction of PTEN, which is what usually happens to other proteins when they interact with Nedd4.
Teaming up, the two groups have now connected the dots. They鈥檝e found that when stroke occurs, PTEN is transported into the cells鈥� nuclei in a process that appears to be dependent on the Ndfip1 protein. And because this relocation does not result in the destruction of PTEN, it returns to the cytoplasm when the neurons are no longer in danger.
Why is this temporary relocation important? When it resides in the cytoplasm of a healthy neuron, PTEN acts as a brake on a cellular pathway that promotes survival and proliferation鈥攁 mechanism that prevents the cell from turning cancerous.
鈥淕etting PTEN out of the cytoplasm and into the nucleus after stroke is a great way to remove this brake and boost the pathway that鈥檚 going to keep the cell alive during trauma,鈥� explains Trotman. The team鈥檚 finding that stroke-induced damage is more severe in mice that can鈥檛 move PTEN into the nucleus than in normal mice underscores the importance of getting this protein out of the way.
鈥淩elocating it temporarily is a much better option than destroying it and getting rid of it permanently, which would make it much harder to reapply the brake when blood supply eventually gets restored,鈥� Trotman says.
These results, recently published in the , have huge implications for stroke therapy. 鈥淏locking PTEN systemically and over a long period of time can be dangerous because that might lead to cancer. But because stroke is an acute, short-lived event, a short-term removal of the PTEN brake in the brain via PTEN-inhibiting drugs might deliver beneficial results in stroke patients,鈥� according to Trotman.
鈥淲e鈥檝e always studied PTEN in the context of how its misregulation (often through mutations) can lead to cancer. This is the first time we鈥檝e seen how PTEN trafficking is regulated by a natural mechanism鈥攂lood supply to tissues,鈥� says Trotman.
His team is now investigating the possibility that this mechanism of PTEN transport into the nucleus might occur in tissues other than the brain in response to fluctuations in blood supply. As obstructions or limitations in blood supply are found in many types of cancer (for example, colon cancer), such a finding could have a big impact on our understanding of cancer progression.