| Grant number: | 03/13189-2 |
| Support Opportunities: | Research Projects - Thematic Grants |
| Start date: | July 01, 2004 |
| End date: | April 30, 2009 |
| Field of knowledge: | Biological Sciences - Biochemistry - Molecular Biology |
| Principal Investigator: | Vilma Regina Martins |
| Grantee: | Vilma Regina Martins |
| Host Institution: | Instituto Ludwig de Pesquisa sobre o Câncer (ILPC). São Paulo , SP, Brazil |
| City of the host institution: | São Paulo |
| Associated research grant(s): | 06/50942-9 - Involvment of cellular prion-stress inducible protein 1 interaction in neural plasticity mechanisms: neuritogenesis, neuroprotection and memory consolidation.,
AR.EXT 06/52103-4 - Different ca2+ signaling pathways mediated by cellular prion protein interaction to laminin gama-1 peptide or stress-inducible protein 1., AR.EXT |
Abstract
The cellular prion protein has been receiving a lot of evidence in the literature not only because its involvement in prion diseases but also due to is biological relevance. Through it is important to note that our group is giving an important contribution in this last aspect. In our previous project we characterized 3 PrPc ligands: laminin and vitronectin at the extracellular matrix and STI1 at the cell surface. The cellular functions related with these interactions and part of the triggered cell signaling were also determined. These results point to a PrPc pleiotropic function probably through a macromolecular complex formed with its ligands. An important result obtained in our last project was the tinding of arare polymorphism at PRNP which is present in 23% of patients with mesial temporal lobe epilepsy related to hippocampal sclerosis (MTLE-HS). Furthermore, patients with MTLE-HS showing this variant alIele had five fold greater chance of remaining intractable after temporal lobectomy. Thus, our results point to many events that must be approached in arder to map all the biological functions related to the celIular prion protein (AU)
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