LIAO PING, MD, Ph.D.
Principal Investigator and Head, Calcium Signalling Laboratory, NNI
Associate Professor (Track IIA-research), Duke-NUS Graduate Medical School
Ph.D. National University of Singapore, 2001
Bachelor of Medicine, Master of Surgery (Neurosurgery)
West China University of Medical Sciences, Sichuan, China, 1996
Contact Information
Calcium Signalling Laboratory, Level 6, Lab 6
National Neuroscience Institute
11 Jalan Tan Tock Seng, Singapore 308433
Tel: (65) 6357 7611 (Office) / (65) 6357 7615 (Laboratory
Fax:(65) 6256 9178
Email: ping_liao@nni.com.sg
The Team
Overview
Cellular ionic homeostasis is a dynamic state regulating ions such as calcium, sodium, and potassium both within the cell and across the cell membrane. As ions determine major brain functions such as firing of action potential, disruption of its homoeostasis worsens tissue damage in diseases of central nervous system such as stroke and head injury. The research in our lab is focused on ion channels and transporters that are key to the disruption of ionic homeostasis in brain disorders. We aim to develop novel treatments to correct the ionic imbalance and translate them into clinical practice which will benefit patients.
One example is Transient receptor potential melastatin member 4 (TRPM4) which is upregulated after stroke. We have shown that TRPM4 inhibition could reduce cerebral edema, a major side effect after reperfusion treatment. A TRPM4 specific antibody M4P was thus developed in our lab against rodent TRPM4 to bind to and block the channel from extracellular space. We demonstrate that M4P could inhibit TRPM4 currents and subsequent cell swelling after hypoxia. In animal model of stroke, M4P was shown to protect vasculature after stroke reperfusion and potentially extend the time window of reperfusion therapy. M4P also exhibits the potential to benefit patients suffered from other brain disorders with hypoxia such as vascular dementia and head injury. As the binding epitope is different between human and rodent TRPM4, a mouse monoclonal antibody M4M against human TRPM4 was developed and verified using a transgenic rat model carrying human TRPM4 sequence. Most recently, humanized antibody was generated from M4M that can be used in patients. We are working to apply this antibody to clinical trials and ultimately to clinical practice for the treatment of patients with hypoxic neurological disorders.
Figure 1. M4P antibody binds to the surface of a cultured live neuron under hypoxia.
About Stroke
Stroke is a leading cause of death and disability worldwide. This medical emergency occurs when blood flow to an area of the brain is cut off. There are two types of stroke, ischemic and hemorrhagic. About 80 percent of strokes are ischemic strokes, caused by the blockage of a cerebral blood vessel.
The goals of treatment of acute ischemic stroke are to restore blood flow. Currently, the only FDA-approved drug for managing ischemic stroke is tissue plasminogen activator (tPA) which must be given to eligible patients within a short time window (<4.5 hours after stroke onset). Patients with tPA treatment have a much better outcome. The earlier the treatment, the better the result. Recanalisation beyond this time window may generate severe side effects such as malignant edema and hemorrhage due to vascular injury.
As time is critical for stroke treatment, recognizing the signs of a stroke can save a life. Use the letters in "FAST" to spot stroke signs and know when to call ambulance: Face drooping, Arm weakness, Speech difficulty, Time to call 995 (Singapore).
Selected Publications (* joint first author, † corresponding author)
Achievements of Students