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ShareOct. 20, 2010 — Precise regulation of tissue architecture is critical for organ function. Single cells build up a tissue by communicating with their environment and with other cells, thereby receiving instructions on whether to divide, change shape or migrate. An interdisciplinary group of researchers from several Max Planck Institutes have now identified a mechanism by which skin cells organize their interior architecture as a response to signals from their surroundings.
Their research is reported in the latest issue of Developmental Cell.
"Cells react to changes in their environment very rapidly. To do this, cells need to have their signaling machinery at the right place at the right time" says Sara Wickström, a researcher from the Max Planck Institute of Biochemistry.
Cellular behavior is controlled by signaling pathways which deliver information derived from the surrounding tissue and other cells to the nucleus and other parts of the cell. In order to achieve both efficient and tightly regulated signaling, cells organize their proteins into distinct cellular compartments. This organization is carried out by intracellular highways called microtubules that are specialized in protein transport.
Sara Wickström from the MPIB in Martinsried is analyzing how signals from the extracellular environment regulate these intracellular highways to allow the transport of specific proteins to their correct location. Genetic analyses in mouse skin revealed that signaling from integrins, cell surface receptors that mediate the interactions of cells with their environment, regulate the organization of microtubules so that they can efficiently deliver proteins the cell surface. This is particularly important in tissues like skin, where the upper surfaces of the cells facing the outside world require a different composition than the lower surface facing the interior of the organism.
In collaboration with Matthias Mann and the Department of Proteomics and Signal Transduction, the exact proteins involved in the process were identified. In addition, expertise provided by Joachim P. Spatz at the MPI of Metals Research in Stuttgart allowed investigating the role of the cell shape in the regulation of microtubules. "The process of protein transport is very complex, and therefore a wide range of different approaches were needed to analyze it," says Sara Wickström.
During diseases like cancer, cells escape normal regulatory mechanisms of cell adhesion and growth signaling to become more motile and proliferative. Changes in the levels of adhesion receptors as well as in the overall protein composition and distribution at the cell surface have long been known to take place in tumor cells.
"The most interesting finding of our study is that all these processes are interregulated. Therefore understanding the basic mechanisms of the regulation might help to tackle the primary causes of these changes during disease," says Sara Wickström. A particularly interesting question is why diseases like cancer become more frequent during ageing, during which structural alterations in the tissues also occur. Sara Wickström will move to start her own research group at the Max Planck Institute for Biology of Ageing in Cologne to continue this interesting avenue of research.
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The above story is reprinted from materials provided by Max Planck Institute of Biochemistry, via AlphaGalileo.
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Journal Reference:
- S. A. Wickström, A. Lange, M. W. Hess, J. Polleux, J. P. Spatz, M. Krüger, K. Pfaller, A. Lambacher, W. Bloch, M. Mann, L. A. Huber and R. Fässler. Integrin-linked kinase controls microtubule dynamics required for plasma membrane targeting of caveolae. Developmental Cell, 2010; 19 (4): 574-588 DOI: 10.1016/j.devcel.2010.09.007
Note: If no author is given, the source is cited instead.
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