Literature DB >> 8915830

Expression of the mRNAs encoding the limbic system-associated membrane protein (LAMP): I. Adult rat brain.

B S Reinoso1, A F Pimenta, P Levitt.   

Abstract

The search for molecular markers common to neural structures that are functionally related has become an attractive strategy for neurobiologists interested in identifying mechanisms involved in the formation of patterned connections. One such molecule is the limbic system-associated membrane protein (LAMP), a 64-68 kDa glycoprotein that is expressed in the soma and dendrites of subpopulations of adult neurons in the brain that are functionally associated with classic limbic structures. Such patterned molecular specificity is established prenatally; LAMP is detected during development on the surface of neurons, axonal membranes and pathfinding growth cones. This molecule has now been cloned (lamp) and has been shown to be highly conserved in rat and human. It is a new immunoglobulin superfamily member that has three Ig domains and a glycosyl-phosphatidylinositol (GPI) anchor to the cell membrane. In this study, the distribution of the lamp transcript in the adult rat brain was determined by using in situ hybridization. Generally, the distribution of lamp corresponds well with that of the LAMP protein. Within the cerebral cortex, the transcript is more abundant in areas that are associated with learning/memory and viscerosensory tasks. It is less abundant in somatic sensory and motor areas. The lamp transcript is also ubiquitous in the basal forebrain, amygdala, and preopticohypothalamic areas. In short, the lamp transcript is expressed heavily in areas of the forebrain and diencephalon that have been classically considered limbic and sparsely or moderately in nonlimbic midbrain and hindbrain regions. Correlative analysis of the connectivity patterns of the regions that express greater amounts of the transcript is consistent with a stronger limbic-associated function relative to the regions expressing less lamp. These quantitative differences may be significant in determining the function of LAMP in the adult brain.

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Year:  1996        PMID: 8915830     DOI: 10.1002/(SICI)1096-9861(19961111)375:2<274::AID-CNE7>3.0.CO;2-#

Source DB:  PubMed          Journal:  J Comp Neurol        ISSN: 0021-9967            Impact factor:   3.215


  9 in total

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Journal:  Proc Natl Acad Sci U S A       Date:  1998-04-28       Impact factor: 11.205

2.  Architectonic subdivisions of neocortex in the gray squirrel (Sciurus carolinensis).

Authors:  Peiyan Wong; Jon H Kaas
Journal:  Anat Rec (Hoboken)       Date:  2008-10       Impact factor: 2.064

3.  Genetic deletion of Lsamp causes exaggerated behavioral activation in novel environments.

Authors:  Elizabeth Haldeman Catania; Aurea Pimenta; Pat Levitt
Journal:  Behav Brain Res       Date:  2007-12-07       Impact factor: 3.332

4.  Differential expression patterns of striate cortex-enriched genes among Old World, New World, and prosimian primates.

Authors:  Toru Takahata; Rammohan Shukla; Tetsuo Yamamori; Jon H Kaas
Journal:  Cereb Cortex       Date:  2011-11-07       Impact factor: 5.357

5.  Neurotractin, a novel neurite outgrowth-promoting Ig-like protein that interacts with CEPU-1 and LAMP.

Authors:  A Marg; P Sirim; F Spaltmann; A Plagge; G Kauselmann; F Buck; F G Rathjen; T Brümmendorf
Journal:  J Cell Biol       Date:  1999-05-17       Impact factor: 10.539

6.  Lsamp is implicated in the regulation of emotional and social behavior by use of alternative promoters in the brain.

Authors:  Mari-Anne Philips; Kersti Lilleväli; Indrek Heinla; Hendrik Luuk; Christian Ansgar Hundahl; Karina Kongi; Taavi Vanaveski; Triin Tekko; Jürgen Innos; Eero Vasar
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7.  Spatiotemporal expression of IgLON family members in the developing mouse nervous system.

Authors:  Sydney Fearnley; Reesha Raja; Jean-François Cloutier
Journal:  Sci Rep       Date:  2021-10-01       Impact factor: 4.379

8.  Limbic system associated membrane protein as a potential target for neuropsychiatric disorders.

Authors:  Jürgen Innos; Kati Koido; Mari-Anne Philips; Eero Vasar
Journal:  Front Pharmacol       Date:  2013-03-26       Impact factor: 5.810

9.  A rare 3q13.31 microdeletion including GAP43 and LSAMP genes.

Authors:  Stefania Gimelli; Massimiliano Leoni; Maja Di Rocco; Gianluca Caridi; Simona Porta; Cristina Cuoco; Giorgio Gimelli; Elisa Tassano
Journal:  Mol Cytogenet       Date:  2013-11-26       Impact factor: 2.009

  9 in total

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