Differential role of APP and APLPs for neuromuscular synaptic morphology and function.

Klevanski, Maja; Saar, Martina; Baumkötter, Frederik; Weyer, Sascha W; Kins, Stefan; Müller, Ulrike C

Klevanski, Maja; Saar, Martina; Baumkötter, Frederik; Weyer, Sascha W; Kins, Stefan; Müller, Ulrike C.

Afiliación

Klevanski M; Department of Bioinformatics and Functional Genomics, Institute of Pharmacy and Molecular Biotechnology, Heidelberg University, Im Neuenheimer Feld 364, 69120 Heidelberg, Germany.
Saar M; Department of Bioinformatics and Functional Genomics, Institute of Pharmacy and Molecular Biotechnology, Heidelberg University, Im Neuenheimer Feld 364, 69120 Heidelberg, Germany.
Baumkötter F; Department of Human Biology and Human Genetics, Technical University of Kaiserslautern, Erwin-Schrödinger-Strasse 13, 67663 Kaiserslautern, Germany.
Weyer SW; Department of Bioinformatics and Functional Genomics, Institute of Pharmacy and Molecular Biotechnology, Heidelberg University, Im Neuenheimer Feld 364, 69120 Heidelberg, Germany.
Kins S; Department of Human Biology and Human Genetics, Technical University of Kaiserslautern, Erwin-Schrödinger-Strasse 13, 67663 Kaiserslautern, Germany.
Müller UC; Department of Bioinformatics and Functional Genomics, Institute of Pharmacy and Molecular Biotechnology, Heidelberg University, Im Neuenheimer Feld 364, 69120 Heidelberg, Germany. Electronic address: u.mueller@urz.uni-hd.de.

Mol Cell Neurosci ; 61: 201-10, 2014 Jul.

Article en En | MEDLINE | ID: mdl-24998676

RESUMEN

The analysis of mouse models indicated that APP and the related APLPs are important for synapse formation and function. The synaptic role of APP is, however, complex due to partially overlapping functions within the gene family. APP/APLPs are proteolytically cleaved and have both adhesive and signaling properties. Mice lacking individual APP family members are viable, whereas APP/APLP2 and APLP1/APLP2 double knockout (DKO) mice die shortly after birth. Here, we analyzed the morphology of the neuromuscular junction (NMJ) of lethal APLP1/APLP2-DKO mice in comparison to lethal APP/APLP2-DKO mutants and viable single KO mice. We report that, surprisingly, the NMJ phenotype of APLP1/APLP2-DKO mice shows striking differences as compared to APP/APLP2-DKO mice. Unexpectedly, APLP1/APLP2-DKO mice exhibit normal endplate patterning and lack presynaptic nerve terminal sprouting. However, at the level of individual synapses we show that APLP1/APLP2-DKO mice exhibit reduced size of pre- and postsynaptic compartments and reduced colocalization. As APP/APLP2-DKO and APLP1/APLP2-DKO mice show similar penetrance of early postnatal lethality, this suggests that deficits at the level of individual synapses due to impaired synaptic apposition and/or deficits in transmitter release may cause lethality. Using an in vitro cell-adhesion assay, we observed that APP trans-dimerization is considerably less efficient than APLP2 trans-interaction. Thus, differences between APP/APLP2 and APP/APLP1 NMJ formation may be in part explained by differences in APP/APLP2 trans-dimerization properties. Collectively, our study further highlights the distinct and essential role of APLP2 at NMJ synapses that cannot be compensated by APP.

Asunto(s)

Precursor de Proteína beta-Amiloide/deficiencia; Regulación de la Expresión Génica/genética; Unión Neuromuscular/citología; Unión Neuromuscular/fisiología; Precursor de Proteína beta-Amiloide/genética; Análisis de Varianza; Animales; Peso Corporal/genética; Distribución de Chi-Cuadrado; Diafragma/citología; Diafragma/metabolismo; Ratones; Ratones Endogámicos C57BL; Ratones Noqueados; Modelos Biológicos; Fragmentos de Péptidos; Receptores Colinérgicos/metabolismo; Médula Espinal/citología; Médula Espinal/metabolismo; Sinapsinas/metabolismo

Palabras clave

Alzheimer's disease; Amyloid precursor protein; Amyloid precursor-like protein; Neuromuscular junction; Synaptic adhesion; Synaptogenesis

Texto completo

Añadir a Mi BVS

Imprimir

XML

PubMed Links

Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Regulación de la Expresión Génica / Precursor de Proteína beta-Amiloide / Unión Neuromuscular Límite: Animals Idioma: En Revista: Mol Cell Neurosci Asunto de la revista: BIOLOGIA MOLECULAR / NEUROLOGIA Año: 2014 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Estados Unidos

Texto completo

Añadir a Mi BVS

Imprimir

XML

PubMed Links

Buscar en Google