How to become a heart cell: Benoit Bruneau

Gladstone Institute for Cardiovascular Disease

Sept. 1, 2013 (Hosted by Osama Ahmed)

Our bodies are made up of around 200 different cell types with very different structures and functions. Paradoxically, every cell contains the same genetic material. During development, proteins called transcription factors turn specific genes on and off. This can force a cell to develop into a brain cell rather than a skin cell, for example. But, when the right genes fail to turn on or when the wrong genes are expressed, developmental defects can occur.

Our guest this month, Dr. Benoit Bruneau, a Senior Investigator at the Gladstone Institute for Cardiovascular Disease, wants to know what makes a heart cell a heart cell. His lab is interested in how these different regulators interact, which factors are required for proper heart development, and which are altered in disease. This work answers important questions about how genes direct development, and it has potential applications for future therapies for heart disease.

More on the Bruneau Lab's research

Stem cells and epigenetics: Barbara Panning

The developing embryo is made up of special cells called stem cells. Unlike most cells, stem cells have the unique ability to transform into specialized adult cells, such as those that make up our heart or the neurons in our brain. In the last five years, scientists have designed a method to go backwards; now the specialized adult cells can be turned into embryonic stem cells. However, a lot of questions remain unanswered. For instance, scientists still do not completely understand what triggers stem cells to transform into different cell types. Or what process keeps stem cells from changing in the first place.
Our guest, Dr. Barbara Panning, a professor in the department of biochemistry at UCSF, is in the process of answering this question. Using a process called RNA interference, her lab turns off specific genes one by one to see how embryonic stem cells are affected. Her research has potentially important implications for diseases like breast cancer.

More on the Panning Lab's research

Hosted by Sama Ahmed

Chronic pain is a disease: Allan Basbaum

Pain helps us avoid potentially harmful situations and is necessary for survival. While most of us only experience acute pain while the painful stimulus is present, some people unfortunately suffer from constant pain that persists long after the stimulus is removed. Our guest this week, Allan Basbaum, a professor and chair of the Department of Anatomy at UCSF, is interested in chronic pain and its cause.

During our interview, Dr. Basbaum explains how pain is in the brain; the pain that one person feels can be more (or less) intense than another person’s perception even if the stimulus is identical. His lab investigates how chronic pain can occur by changes in the nervous system and the role of epigenetics (the interactions between your DNA and all other non-DNA elements). They are also interested in transplanting inhibitory precursor cells (cells that develop and eventually inhibit the activity of surrounding neurons) to help the spinal cord suppress pain signals. His findings could eventually lead to effective therapies to treat this debilitating disease.

More on the Basbaum Lab's research

Hosted by Osama Ahmed