Clues to γ-secretase, huntingtin and Hirano body normal function using the model organism Dictyostelium discoideum
© Myre; licensee BioMed Central Ltd. 2012
Received: 3 February 2012
Accepted: 10 April 2012
Published: 10 April 2012
Many neurodegenerative disorders, although related by their destruction of brain function, display remarkable cellular and/or regional pathogenic specificity likely due to a deregulated functionality of the mutant protein. However, neurodegenerative disease genes, for example huntingtin (HTT), the ataxins, the presenilins (PSEN1/PSEN2) are not simply localized to neurons but are ubiquitously expressed throughout peripheral tissues; it is therefore paramount to properly understand the earliest precipitating events leading to neuronal pathogenesis to develop effective long-term therapies. This means, in no unequivocal terms, it is crucial to understand the gene's normal function. Unfortunately, many genes are often essential for embryogenesis which precludes their study in whole organisms. This is true for HTT, the β-amyloid precursor protein (APP) and presenilins, responsible for early onset Alzheimer's disease (AD). To better understand neurological disease in humans, many lower and higher eukaryotic models have been established. So the question arises: how reasonable is the use of organisms to study neurological disorders when the model of choice does not contain neurons? Here we will review the surprising, and novel emerging use of the model organism Dictyostelium discoideum, a species of soil-living amoeba, as a valuable biomedical tool to study the normal function of neurodegenerative genes. Historically, the evidence on the usefulness of simple organisms to understand the etiology of cellular pathology cannot be denied. But using an organism without a central nervous system to understand diseases of the brain? We will first introduce the life cycle of Dictyostelium, the presence of many disease genes in the genome and how it has provided unique opportunities to identify mechanisms of disease involving actin pathologies, mitochondrial disease, human lysosomal and trafficking disorders and host-pathogen interactions. Secondly, I will highlight recent studies on the function of HTT, presenilin γ-secretase and Hirano bodies conducted in Dictyostelium. I will then outline the limitations and future directions in using Dictyostelium to study disease, and finally conclude that given the evolutionary conservation of genes between Dictyostelium and humans and the organisms' genetic tractability, that this system provides a fertile environment for discovering normal gene function related to neurodegeneration and will permit translational studies in higher systems.
KeywordsDictyostelium discoideum Model organism Neurodegeneration Huntingtin Presenilin γ-secretase Hirano bodies Neurotransmitter homologues
Dictyostelium - emergence of a classic model organism for the study of neurodegenerative disease
Alzheimer's disease: The amyloid precursor protein and discovery of presenilin-dependent γ-secretase activity
Alzheimer's disease (AD) is the most common cause of dementia, estimated to contribute to about 60 to 70% of cases . AD is a terminal disease that culminates in death. Impaired recent memory usually is an initial symptom of AD, but other cognitive deficits (e.g., changes in attention, problem-solving abilities) may also be present. Amyloid plaques and neurofibrillary tangles, the characteristic pathological hallmarks of AD, are believed to be causative and accrue in the years preceding clinical symptoms. Amyloid plaques are accumulations of insoluble protein aggregates in the extracellular space of the brain and the primary component of plaques is the Aβ peptide, a 38- to 43-amino acid peptide derived from the larger pre-cursor protein APP [13, 14]. Mutations in APP [15, 16] and two other genes, presenilin-1 (PSEN1)  and presenilin-2 (PSEN2), have been identified that result in autosomal dominant forms of early-onset FAD . The intimate relationship between APP and the presenilins in the production of Aβ is beyond the scope of this review but is detailed elsewhere . The presenilins are homologous, ubiquitously expressed multiple transmembrane domain proteins and many seminal reports provide compelling evidence that presenilins provide the catalytic core of γ-secretase [20–23]. The protein composition of the γ-secretase complexes have been resolved and each consist of four proteins that are all required for proteolytic activity [24–26]: APH-1, PEN2, and nicastrin [25, 27]. The normal biological function of the presenilins has been difficult to determine largely due to the fact that it is essential and knockout mice die in utero. To fully understand and appreciate the normal in vivo function of the presenilins they must be studied in the context of organismal models including Dictyostelium.
The identification of presenilins and γ-secretase activity in Dictyostelium
The presenilin γ-secretase complexes regulate cell differentiation and phagocytosis in Dictyostelium
This work demonstrates the evolutionary conservation of this key regulatory enzyme. The most obvious value stemming from this work for the study of presenilin function are the possibilities for elucidating presenilin-independent function(s) as wild-type presenilins are required for proper protein degradation through the autophagosome-lysosome system thereby implicating a role for these proteins in autophagy ; secondly, the exciting prospects surrounding the finding that proteolytic processing of APP occurs in Dictyostelium exactly the same way as has been shown animal cells. This finding is important not only because it provides an excellent system in which to test therapeutic agents that target Aβ production in vivo, but it is remarkable that this enzyme, given the evolutionary distance between Dictyostelium and humans, is capable of cleaving a non-endogenous substrate to produce C-terminal fragments and ratios of secreted Aβ40/Aβ42 identical to mammalian systems. Knowledge gained about human diseases including cancers from the use of yeast cannot be denied, and with Dictyostelium, we also have an equally genetically tractable organism that not only contains genes uncannily similar to humans, but as a single cell behaves much like an animal cell and further offers the ability to study gene function under conditions of multicellularity all in the same model. Even with the evolutionary distance between humans and Dictyostelium one might expect genes to play different roles, but with regard to amyloidogenic processing of APP, this does not appear to be the case. It should be mentioned that a survey of the Dictyostelium genome does not readily identify or predict the presence of either the known α-secretase or β-secretase  and suggests the presence of yet to be identified first-cleavage sheddases either unique to Dictyostelium or potentially conserved across metazoan species. Moreover, this model offers a biochemical clarity not offered by any other system to date to study γ-secretase function directly, free from the multiple secondary effects that can arise from aberrant proteolytic processing of more than 60 identified substrates . This study provides strong in vivo evidence for presenilin function in regulating phagocytosis, only previously suspected in animal cell culture . Lastly, with the availability of Dictyostelium strains carrying multiple loss-of-function mutations to the components of the γ-secretase, this model system allows for the rapid systematic analysis of how specific mutations to human presenilins might result in gain-of-function or loss-of-function effects that can be readily assessed in higher models. Further studies will be required to determine whether the mammalian PSEN gene can rescue Dictyostelium ps1-null phenotypes and proteolytic processing of human APP.
Higher organism and cellular models of Huntington's disease
Huntington's disease (HD) is a fatal neurodegenerative disease  also known as Huntington's chorea, that affects muscle coordination from preferential loss of efferent medium spiny neurons in the striatum of the basal ganglia, leads to cognitive decline, dementia and eventually death [36–38]. Genetic evidence suggests the disease is caused by an unstable CAG trinucleotide repeat within the coding region of the htt gene leading to expansion (> 35) of glutamine (Q) residues near the amino-terminus of the protein . Mutant HTT confers an unknown gain-of-function property to the protein, but might also impair normal protein function . Huntingtin is a large (350 kDa) alpha-solenoid HEAT (h untingtin, e longation factor 3, the A subunit of protein phosphatase 2A, and T OR1) repeat protein  with little resemblance to any known protein. The normal function of HTT, the nature of the polyQ mutation which is expressed in both neuronal and non-neuronal cells and how it contributes to pathogenesis still remains unclear . Although genetically precise mouse models for HD have contributed significantly towards understanding HTT normal function, these mice are expensive to create, to maintain and therefore difficult to recapitulate results. Thus, defining the disease-producing 'gain-of-function' - either a polyglutamine-length dependent increase or deregulation of a normal huntingtin activity or the introduction of a novel polyglutamine-length dependent activity, will require an understanding of the protein's normal function(s).
A wide range of HD animal models are currently available and have been used to investigate pathological pathways, molecular targets, and potential therapeutics. Invertebrates such as Drosophila melanogaster, non-mammalian species (e.g., Danio rerio) and mammals, including mice, rats, sheep and non-human primates, have been genetically engineered to model the HD mutation. Although these systems are extremely important tools to understand HD, a large majority of studies focus upon the late end-stage disease symptoms and thus offer minimal insight into early manifestation including HTT normal function. The existence of HD cell lines has been, to a finite degree, useful for the dissection of huntingtin function and assessment of potential therapeutic compounds [42, 43]. Further, in vitro cell lines often do not show overt defects suggesting they are unable to reproduce the pathophysiological mechanisms induced by the mutant gene.
Many established model systems are based upon an amino-terminal fragment that results in perturbation of many cellular processes but these remove the polyglutamine tract from its normal protein context. Therefore, one cannot understate that strategies are badly needed to reveal full length huntingtin-dependent biochemical processes that contribute to HD pathology. Because of the evolutionary conservation of huntingtin, lower organism systems offer an attractive and affordable route that has yet to be exploited to understand huntingtin function.
The identification of Dictyostelium huntingtin
The Dictyostelium genome was screened and found to contain a single gene with sequence homology to human huntingtin. Bioinformatic and phylogenetic analysis of the primary amino acid sequence placed the protein firmly within the huntingtin family, including size, and the presence of numerous HEAT and HEAT-like repeats. Dictyostelium mutants' deficient for HTT cells are viable, unlike the embryonic lethality seen in higher eukaryotes, but are fragile in that they display a number of subtle phenotypes suggesting that HTT is involved in a number of cellular processes . We show that huntingtin deficiency impacts upon osmoregulation, cation homeostasis, cell motility, cell shape, chemotactic cAMP relay, homotypic cell-cell adhesion, cell fate determination and cytokinesis in Dictyostelium [9, 44]. Importantly, these phenotypic deficits are greatly dependent upon the environment in which the cells are placed which suggests that HTT aids in translating extracellular signals into cellular processes. These findings support the large body of evidence that suggest in metazoa, huntingtin is a multifunctional protein with roles in embryogenesis, cell fate, cytoskeleton, apoptosis, vesicular and mitochondrial transport, iron homeostasis, autophagy, energy metabolism and transcriptional regulation [39, 41, 45, 46]. A major issue of concern is which, if any, of these functions directly involve HTT or are secondary effects to HTT deficiency or mutant HTT activity. The power behind the Dictyostelium system is that it allows for the identification of in vivo HTT functions at the level of both single cells and a multi-cellular environment all in the same organism with a biochemical and cellular clarity to identify functions that directly depend on HTT.
Dictyostelium cells deficient for huntingtin display cell shape and cytoskeletal defects
When htt- cells are placed under low ionic strength phosphate buffer, the cells elicit a round phenotype without membrane extensions, a reduction of F-actin at the cortex of the cell and under hypoosmotic conditions rapidly swell and undergo complete lysis within 5-6 h . This fits well with reports that mutant HTT in cells from HD patients or when normal huntingtin levels are reduced, cells display defective actin-remodeling under conditions of stress  and consistent with mammalian studies that huntingtin regulates neurological processes including actin-rich dendritic spine formation and membrane branching [48, 49]. In vitro binding of the HTT N-terminus to F-actin has been reported  and may indicate a normal, perhaps transient, function for HTT in the regulation of the actin cytoskeleton. Dictyostelium provides a valuable tool to uncover mechanisms by which HTT regulates actin-cytoskeleton responses.
Huntingtin modulates chemotaxis in Dictyostelium
The failure of htt- cells to osmoregulate and sensitivity to extreme hypoosmotic shock secondarily affects intracellular ion homeostasis. As a consequence, unless specific cations (Ca2+ or Mg2+) are provided exogenously htt- cells appear unable to initiate cAMP-induced Ca2+-transients that may act in a feedback loop to positively reinforce cAMP relay which impairs chemotaxis during Dictyostelium development. Although the a role for HTT in chemotaxis has not been established in mammalian systems, a consensus is gradually emerging that the dyshomeostasis of Ca2+ is an important factor in the linkage of the HTT mutation to the onset and progression of the disease  and together suggest abnormal Ca2+ signaling and other Ca2+ signaling proteins should be explored further as an evolutionary conserved role for HTT.
Huntingtin regulates cell fate during development in Dictyostelium
Insight into Hirano bodies - Dictyostelium discoideum
Hirano bodies, described about 40 years ago, are bright eosinophilic intracytoplasmic inclusions/protein aggregates with crystalloid fine rod structures that occur preferentially in the neuronal processes of individuals with neurodegenerative diseases including Alzheimer's disease, Creutzfeldt-Jacob disease, amyotrophic lateral sclerosis, parkinsonism-dementia and Pick's disease [54, 55]. Hirano bodies are largely considered a pathological hallmark of postmortem brain samples from patients suffering from neurodegenerative disorders representing "tombstones" of neuronal cell death. Hirano bodies have been reported in glial cells, in peripheral nerve axons and in extraocular muscles of eyes  suggesting they are more than products of cell death. It should be noted that Hirano bodies, as a function of age, appear in individuals without neurodegeneration . Hirano bodies are complex inclusions comprised of many proteins including actin and actin-associated proteins (cofillin and alpha-actinin), tau, a C-terminal fragment of APP; microtubule associated bundling proteins, and neurofilaments . Moreover, they have been described in various experimental animals. Understanding the underlying pathological molecular mechanism responsible for their formation has been precluded by the lack of either an in vitro or in vivo experimental model system.
Research using Dictyostelium revealed that formation of Hirano bodies is a pathological event . The expression in Dictyostelium of the CT fragment (amino acids 124-295) of the 34 kDa protein, the 34 kDa protein is one of 11 actin crosslinking proteins present in Dictyostelium, a protein that exhibits activated actin binding and calcium-insensitive actin filament cross-linking activity induced cells to form ellipsoidal paracrystalline inclusions that contain ordered assemblies of F-actin, CT-myc, myosin II, cofilin and alpha-actinin that remarkably resembled the structure of Hirano bodies. They extended their findings to mammalian murine cells and discovered that F-actin rearrangements caused by a reduction in stress fibers accumulate as numerous punctate foci and large aggregates: Hirano bodies . So the failure to regulate either the activity and/or affinity of an actin cross-linking protein provides a signal that forms Hirano bodies. Whereas wild type cells complete development in 24 h, CT-myc cells contained significantly higher amounts of F-actin, formed fruiting bodies with delayed developmental timing by ~6 h. The accumulation of F-actin was also shown to occur in murine cells expressing CT-myc. This report established for the first time that Hirano bodies are not restricted to mammalian cells or nerve cells occur because of aberrant function of the actin cytoskeleton and that Hirano bodies can exert defects on normal cell function. Because of using Dictyostelium, Hirano bodies and induction of F-actin rearrangements in mammalian cell cultures by expression of the CT 34-kDa actin-bundling protein was found to occur in HEK 293, HeLa, Cos7 cells, neuroblastoma and astrocytic cells, and in primary neurons .
Several Dictyostelium genes are homologous or retain a significant amount of structural conservation to human genes making the organism a useful biomedical model system. With the entire genome sequenced and publicly available in a model organism database called dictyBase, it allows molecular and cellular biologists to examine with more clarity the complex multifunctional aspects of gene function. However, one limitation of using unicellular organisms (e.g., yeast) as models for assessing the function of genes involved in disease is that pathologies which affect specific organs cannot be as readily assessed as it might be in the relevant organism. This limitation may also apply to genes that are present in unicellular organisms but are required in a more stringent manner in specialized tissues, or expressed as a variety of different isoforms in specific cell types. However, this limitation has not precluded the use of lower organisms to understand cell division and cancers in many different organs. Although Dictyostelium develops into bona fide multicellular organism, it does present a limitation in the number of cell types that can be analyzed and therefore discoveries made using this organism must be rigorously assessed in the relevant mammalian cell type. Coupled with translational experiments and validation in higher eukaryotes, research using Dictyostelium will expedite and contribute to our understanding of human neurological diseases. Individual cell behavior accounts for the many phases of health and pathogenic mechanisms that initiate disease. This has been elegantly portrayed in Dictyostelium with respect to the precise production of Aβ from the heterologous expression of human APP. Chemotaxis is a critical cellular function with implications in embryogenesis. Dictyostelium cells deficient for HTT show highly defective chemotactic behavior coupled with cytoskeletal/membrane deficits under conditions of low ionic conditions that may reveal conserved roles for this protein in axon guidance, neuritic extensions and embryogenesis. Future endeavors that increases the amount of translational research conducted in higher organisms or neuronal cell models will be beneficial for understanding both Dictyostelium cellular physiology and, more importantly, the cellular mechanisms of human disease. I wish to posit that multiple model systems can and should be employed in the cross-genomic analysis of human neurodegenerative disease genes to address multiple basic eukaryotic cellular functions (e.g., Dictyostelium), to their assembly into various types of more complex molecular pathways (e.g., flies and worms), and then validated and assessed in models of human neurodegenerative disease (e.g., mice).
Amyloid precursor protein
Cyclic adenosine monophosphate
Familial Alzheimer's disease
Huntingtin: elongation factor 3: the A subunit of protein phosphatase 2A: and TOR1.
I wish to thank Marcy E. MacDonald and James F. Gusella for their support, foresight in using this particular model organism and numerous insightful, scientific discussions.
MM was supported by grants NINDS NS032765, Massachusetts HD Center Without Walls NS016367, Huntington's Disease Society of America Coalition for the Cure, and the CHDI Foundation.
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