After a natural disaster like a big fire, countless helpers work together to get rid of debris, to build temporary shelters and to provide food for people in need. When a cell is exposed to dangerous environmental conditions such as high temperatures or toxic substances, a quite similar process is initiated: the cellular stress response, also called heat shock response.
Together with colleagues from the Technical University of Dresden, scientists of the Max Planck Institute of Biochemistry in Munich-Martinsried could uncover an entire network of cellular helpers and thus identify new regulatory mechanisms of this stressresponse. “Our results could also be of use for investigating neurodegenerative diseases such as Alzheimer’s or Parkinson’s,” hopes Christian Loew, PhD student at the MPI of Biochemistry. The study has now been published in the journal Cell.
When an organism is exposed to life-threatening conditions, it sounds the alarm and a cellular emergency program, the heat shock response, is initiated. However, the name “heat shock response” is misleading. In the beginning of the 1960s, this form of stressresponse was first observed. Scientists exposed fruit flies to high temperatures and discovered a complex emergency program designated to save single cells and thus the organism itself. Today researchers know that this program is also triggered by other dangers such as radiation or toxic substances. The terminology, however, is still in use.
During the heat shock response, different stressproteins are synthesized. Their task is to prevent permanent damage to the organism. “You can compare it to an emergency alert. In order to restore the original status as soon as possible, problems and damages are identified, counter-measures initiated and coordinated”, Loew describes the processes in the cell. In a comprehensive analysis, the Max Planck scientists have investigated 15 000 proteins and their role in the heat shock response. They could show that the helpers are organized in different groups according to their tasks and disaster zones. One group of proteins, for instance, checks whether the DNA in the nucleus is still intact.
The protein HSF1 (short for heat shock transcription factor) is responsible for the central coordination of the disaster management. In the moment it is activated, it calls a variety of other proteins into action to eliminate the damages. The scientists could demonstrate two ways in which this control center in itself is regulated. When the crisis is overcome, HSF1 is degraded by the cell’s waste disposal system, the proteasome. As long as there is still damage to get rid of, another protein (Acetyltransferase EP300) prevents the degradation.
The understanding of the heat shock response could also be of interest for neurodegenerative diseases such as Alzheimer’s or Parkinson’s, so the scientists in Martinsried hope. Typical for these diseases are massive cell damages and, thus, the excessive demand on the cellular quality control. Nerve cells die and cannot fulfill their tasks in the brain anymore. “A targeted activation of the heat shock response could reduce the disease specific cell damages,” explains Loew.
S. Raychaudhuri, C. Loew, R. Körner, S. Pinkert, M. Theis, M. Hayer-Hartl, F. Buchholz and F. U. Hartl: Interplay of Acetyltransferase EP300 and the Proteasome System in Regulating Heat Shock Transcription Factor 1. Cell, February 27, 2014. DOI: 10.1016/j.cell.2014.01.055