Smith laboratory: Cardiac Form and Function

Research Overview

View A/Professor Smith's latest publications listing here

Our survival is contingent on a correctly formed and functioning heart. It’s architecture is so precise that even small deviations from its normal structure can have debilitating or even fatal consequences. The complexity of the heart is achieved during embryonic development, beginning as sheets of cells that proliferate, migrate, differentiate and reorganise in an exact sequence of events to form the final functional organ. The entire process is controlled by a reproducible genetic program, evidenced by the fact that each baby born has a heart with stereotypical architecture. The building of this organ is not always perfect and when mistakes occur during embryonic development, it results in congenital heart defects (or structural defects of the heart). There is a large genetic contribution to congenital heart defects, whereby genes that are essential for heart development may harbour mutations and, therefore, malfunction, preventing the normal progress of heart development. In addition to forming the correct structure, the heart must also beat with co-ordinated rhythm. This is also established during embryonic development. The electrical tissues within the heart are patterned and partitioned to permit asynchronous beating of the organ (whereby the atria beat first, followed by the ventricles, permitting onward propulsion of the blood). Defects in the correct patterning of these tissues or mutations in genes that encode electrical machinery (such as ion channels and gap junctions) result in cardiac arrhythmia.

The goal of the Smith laboratory is to identify the genes that are required for cardiac development and rhythm and to understand how these genes function. The lab uses both forward and reverse genetics approaches to create mutants with cardiac defects. By studying and intervening with the phenotypes of these mutants, we gain understanding into the timing of disease onset, the genetic pathways the affected gene operates in, and molecular mechanisms and cellular contexts of gene function. We primarily use the zebrafish model for gene discovery efforts and in vivo imaging, and branch into creating mouse models as the project demands. Building this basic knowledge of how the heart forms and how disease can manifest, puts us in great stead to diagnose, interpret and devise strategies to treat genetic cardiac diseases.

Staff

A/Prof Kelly Smith, Research Fellow and Head of Lab

Collaborators

Prof Jeroen Bakkers, Hubrecht Institute, Netherlands

Prof Didier Stainier, Max Planck Institute, Germany

A/Prof Duncan Sparrow, Oxford, UK

Prof Arie Verkerk, Amsterdam Medical Centre, Netherlands

Prof Diane Fatkin, Victor Chang Cardiac Research Institute, NSW

Prof Christopher Semsarian, Centenary Institute, NSW

Prof Rob Parton, The University of Queensland

Prof Ben Hogan, Peter Mac & The University of Melbourne

Dr Nathan Palpant, The University of Queensland

Dr Cas Simons, Murdoch Childrens Research Institute

A/Prof Mathias Francois,The University of Queensland

Research Opportunities

This research project is available to PhD students to join as part of their thesis.
Please contact the Research Group Leader to discuss your options.

Research Projects

This Research Group doesn't currently have any projects



Faculty Research Themes

Child Health

School Research Themes

Cardio-Respiratory, Cell Signalling, Molecular Mechanisms of Disease



Key Contact

For further information about this research, please contact Head of Laboratory Associate Professor Kelly Smith

Department / Centre

Physiology

Unit / Centre

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