FERNANDEZ-FUNEZ LAB

The Fernandez-Funez Lab aims to unravel the molecular mechanisms underlying neurodegeneration using Drosophila models of several proteinopathies. Our lab uses the power of genetics to do discoveries and we also utilize neuroscience, cell biology, molecular biology, protein biochemistry, imaging, histology, and behavioral techniques to conduct comprehensive studies on relevant genes implicated in neurodegeneration.

Whole-mount immunofluorescence of a Drosophila brain expressing expanded Huntingtin (Htt-128Q) in the brain

Whole-mount immunofluorescence of a Drosophila brain expressing expanded Huntingtin (Htt-128Q) in the brain (magenta). The mushroom bodies are weakly stained. In green, DAPI labels neuronal nuclei in the cortex.

3D rendering of the mushroom bodies (MB) of the fruit fly

3D rendering of the mushroom bodies (MB) of the fruit fly (front). The MB are the dorsal and medial projections of 2,500 neurons (Kenyon cells) in the back of the head. This nerve center plays a key role in olfactory memory and learning in Drosophila.

3D structure of the globular domain of the prion protein (PrP) from Hamster and dog .

3D structure of the globular domain of the prion protein (PrP) from Hamster (left) and dog (right). One amino acid change at position 159 introduces local and long-distance structural changes to the globular domain and confers resistance to prion diseases.

Expression of the hamster prion protein (HaPrP)

Expression of the hamster prion protein (HaPrP) induces progressive, vacuolar degeneration in the synapses of the Drosophila brain. Left, 1-day old fly expressing HaPrP shows a healthy synaptic bouton (blue colored) from a projection neuron (PN) surrounded by dendrites from mushroom body neurons. Right, After 30 days, the synaptic boutons look swollen, lack active zones, and contain abnormal mitochondria and vesicular bodies.

Flies expressing the toxic amyloid-β42 (Aβ42) peptide found in the Alzheimer’s disease brain induce a small and glassy eye that is rescued by co-expression of the ER-stress factor XBP1 (Hum Mol. Gen 2011).

Flies expressing the toxic amyloid-β42 (Aβ42) peptide found in the Alzheimer’s disease brain induce a small and glassy eye that is rescued by co-expression of the ER-stress factor XBP1 (Hum Mol. Gen 2011).

Flies expressing the toxic amyloid-β42 (Aβ42) peptide found in the Alzheimer’s disease brain disrupt the organization of the retina, resulting in short photoreceptors (box) and fused lenses (arrow)

Flies expressing the toxic amyloid-β42 (Aβ42) peptide found in the Alzheimer’s disease brain disrupt the organization of the retina, resulting in short photoreceptors (box) and fused lenses (arrow)

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  • Research

    A large group of human neurodegenerative conditions are associated to protein deposition in the brain. Some of the most common brain conditions include Alzheimer’s, Parkinson’s, and Huntington’s disease, all of which are devastating and incurable. Prion disorders are rare and transmissible, but belong to the same class of neurodegenerative diseases. The common feature of these and many other diseases is the deposition of misfolded proteins in brain neurons proposed to be responsible for neuronal cell death. The proteins responsible for each disease (Amyloid-beta in AD, alpha-Synuclein in PD, Huntingtin in HD and the Prion protein in PrD) are quite different in sequence, function and cellular localization. However, they are all structurally unstable and prone to misfold, thus exposing hydrophobic pockets that make the proteins aggregate. Upon autopsy, these proteins accumulate in large, fibrillar aggregates that were originally thought to be responsible for neurodegeneration. However, the focus has recently turned to smaller, soluble aggregates (oligomers) that are highly toxic and seem capable of disrupting synaptic function. This knowledge, though, has not resulted in significant insight into the causes of neuronal cell death nor has produced effective therapies.

    I am using the flexibility and genetic prowess of Drosophila to gain knowledge on some of the most intractable questions posed by this group of neurodegenerative diseases. Recent work includes the identification of engineered antibodies and chaperones that bind amyloid-beta and efficiently suppress its toxicity. I also generated a robust phenotypic Drosophila model expressing the prion protein in the eye that I will use to conduct genetic screens to identify genetic modifiers of PrP neurotoxicity. I am also interested in uncovering the pathogenic mechanisms mediating the toxicity of several genes implicated in amyotrophic lateral sclerosis (ALS).

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    Name: Pedro Fernandez-Funez, PhD
    Associate Professor, Medical School, Duluth Campus
    Title:
    Principal Investigator
    Email:
    pfernand@d.umn.edu
    Phone:
    218-726-6863
    Office Address:
    Department of Biomedical Sciences
    1035 University Drive
    SMED 333
    Duluth, MN 55812
    Photo:

    Pedro Fernandz-Funez