Faculty Advisor

Jain, Anjana

Abstract

Rett Syndrome (RTT) is an autism-spectrum disorder caused by a mutation in the gene coding for methyl-CpG-binding protein 2 (MeCP2). In accordance with the theory that RTT arises from a excitatory/inhibitory imbalance caused by dendritic alterations, we hoped to observe reduced arborization in the MeCP2 mutant neurons. The dendritic morphology of pyramidal cells and interneurons proceeding from MeCP2 mutant and non-mutant mice were reconstructed and analyzed. We observed a possible difference in the area covered by the basal dendritic arborization and decreased dendritic complexity reflected in diminished process lengths and number of terminal segments. This could translate to a diminished integrative capacity in MeCP2 KO cells.

Publisher

Worcester Polytechnic Institute

Date Accepted

March 2013

Major

Biomedical Engineering

Project Type

Major Qualifying Project

Accessibility

Unrestricted

Advisor Department

Biomedical Engineering

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