Brian D Ackley

Brian Ackley
  • Associate Professor
  • MB Research Coordinator

Contact Info

5004 Haworth Hall
1200 Sunnyside Ave.
Lawrence, KS 66045


Ph.D., Northwestern Institute for Neuroscience, 2001, Chicago, IL
B.A. in Chemistry and Psychology, Virginia Polytechnic Institute and State University, 1994, Blackburg, VA


Interactions between neurons and their environment during development Cell Adhesion Molecules Drive Neuronal Development: Our brains are an amazing network of cells, connected by axons and dendrites that form the conduits for our thoughts and actions. One of the fundamental questions of neuroscience is to understand how these connections form. As such these cells and their processes must differentiate appropriate partners from inappropriate targets. The fidelity with which this happens is truly astounding. Neuroscientists have found that molecules outside the cells instruct all the stages of neural development. For example growth factors secreted from other cells instruct nerve cells to adopt the correct fate, diffusible cues inform neurons where potential synaptic partners might be located and cell surface cues can tell them when they have reached their targets. Work in the Ackley Lab seeks to understand the contribution of cell adhesion molecules to the process of neural development, and we use genetics, cell biology and biochemistry to approach to this problem. 1. Flamingo/Celsr Flamingo is a member of an evolutionarily conserved family of molecules called cadherins. We have found that theC. elegansflamingo member, FMI-1,contributes to the axonal outgrowth and synapse formation of GABAergic motorneurons. We have also found that another conserved cadherin protein, CDH-4, appears to function in the FMI-1 pathway. Little is known about how cadherins interact heterotypically, while much more is known about how they interact homotypically. 2. Calcium-dependent Synapse Formation Previously we have found that the conserved basement membrane protein, nidogen, and a cell-surface receptor, LAR, function in maintaining the morphology and position of neuromuscular junctions (NMJs) inC. elegans. In a genetic modifier screen we have found that molecules in a calcium signaling pathway, including a voltage gated calcium channel, the calmodulin kinase II (CaMKII) and a conserved calcium binding protein, calmyrin, function in this pathawy. Mutations that ablate the function of the calcium signaling pathway can suppress morphological defects caused by nidogen mutations. In cases where the calcium pathway is hyperactivated they mimic the loss of nidogen. Our lab has recently been using time-lapse confocal micrsocopy to visualize GABAergic NMJs during development, and coupling that with mutations in molecules that regulate their formation. 3. RNAi of Cell Adhesion Molecules Using a bioinformatic approach we have created a list of all of the genes in the C. elegans genome predicted to be secreted into the extracellular space. This list (The Secretome) includes ~10,000 members. To facilitate understanding how each of these may contribute to development we are creating a library of RNAi clones directed against each member of the list. Ultimately this will provide a valuable rescoure to investigators wanting to probe the contribution of secreted molecules to pathways of interest. C. elegansas a Model forin vivoMedicinal Probe Development Beyond their utility as a genetic model organism,C. eleganshave vast potential to develop flourescent molecular probes. We collaborate with Dr. Blake Peterson(KU Medicinal Chemistry)to develop, assay and validate molecular probes and their targets. Our research groups were awarded one of the highly competetive NIH Challenge Grants in 2009 to facilitate the start of this project.