Mild head trauma, including concussion, can lead to chronic brain dysfunction and degeneration but the underlying mechanisms remain poorly understood. Here, we developed a novel head impact system to investigate the long-term effects of mild head trauma on brain structure and function, as well as the underlying mechanisms in Drosophila melanogaster. We find that Drosophila subjected to repetitive head impacts develop long-term deficits, including impaired startle-induced climbing, progressive brain degeneration, and shortened lifespan, all of which are substantially exacerbated in female flies. Interestingly, head impacts elicit an elevation in neuronal activity and its acute suppression abrogates the detrimental effects in female flies. Together, our findings validate Drosophila as a suitable model system for investigating the long-term effects of mild head trauma, suggest an increased vulnerability to brain injury in female flies, and indicate that early altered neuronal excitability may be a key mechanism linking mild brain trauma to chronic degeneration.
Repetitive head trauma, including mild injuries such as concussion, is a risk factor for developing several neurodegenerative disorders, including Alzheimer’s disease (AD)1,2, Parkinson’s disease (PD)3, Amyotrophic lateral sclerosis (ALS)4 and chronic traumatic encephalopathy (CTE)5,6,7,8,9. Although each of these conditions arise from distinct etiologies, they share some common features including abnormal protein deposits3,4,10,11, impaired axonal transport12, swelling13 and retraction14, immune cell activation, and excitotoxicity15,16,17,18,19,20,21,22, which ultimately result in progressive cellular degeneration, cell death, and frank brain atrophy. Symptomatic onset typically appears later in life in each of these aforementioned diseases, yet neurodegeneration is believed to begin years in advance23,24. While repetitive head trauma is a risk factor for developing neurodegeneration, it remains a challenge to provide a causal link between the mechanisms underlying the early injury response and chronic cellular and behavioral sequelae. A more complete understanding of the brain’s response to injury over time will lend new insight towards the development of neuroprotective strategies.
The use of rodent models is a common method to study the basic pathophysiological mechanisms of traumatic brain injury16,25,26,27,28,29,30,31,32, but the relatively long rodent lifespan together with the use of surgical procedures for delivering injuries27,33 represent a challenge to investigate the onset and progression of lifelong effects following head trauma. Here, we developed a tractable Drosophila melanogaster (fruit fly) model that enables lifelong interrogation of specific processes and their downstream cellular and behavioral effects. Fruit flies represent an excellent tractable model organism to dissect fundamental cellular and molecular disease mechanisms, including neurodegeneration34,35,36, while taking advantage of their relatively short lifespan37,38,39,40,41,42 that enables long-term outcome analyses related to head injury exposure. Several fly models have been developed to study traumatic brain injury in Drosophila, but the lack of controlled head-specific impacts may confound neuronal-specific responses43,44,45. Head-specific impact models have recently been developed in which physical head impacts were delivered to the heads of individually restrained flies46,47,48, but no long-term study was carried out to examine the detrimental effects that might develop later in life.
In this study, we devised a novel injury model with high precision and accuracy in delivering repetitive headfirst impacts to a large number (10–15 flies at a time) of awake and unrestrained fruit flies. We then applied this model to investigate novel mechanisms related to repetitive mild head impacts on lifelong function in both sexes. We established that early exposure to repetitive mild head impacts resulted in long-term behavioral dysfunction and brain degeneration, which is more pronounced in female flies. We further investigated an underlying mechanism and identified neuronal activity as a key mediator for mild trauma-induced long-term brain dysfunction. Together, this work provides a causal relationship between the early phase of injury involving neuronal activity and the subsequent chronic degenerative processes.
Materials and methods
Flies were maintained at 18 °C (activity-suppressing experiments) or 25 °C, with 60% humidity on a 12-h:12-h light:dark cycle and kept in vials containing fresh fly media consisting of cornmeal, yeast, molasses, agar, p-hydroxy-benzoic acid methyl ester. Vials were changed every 3–4 days using sterile methods. The following stocks were used: w1118 (BDSC 5905), UAS-CaLexA-LUC49 (from K. Abruzzi), OK107-GAL4 (BDSC 854), neuronal synaptobrevin-GAL4 (nSyb-GAL4)50 (from T. Ngo), nSyb-LexA50 (from T. Ngo), LexAop-Shibirets150 (from T. Ngo), Oregon R (BDSC 5) and UAS-Transformer (BDSC 4590). A stable line expressing nSyb > Shibirets1 (LexA > LexAop) was created using the respective aforementioned stocks and used for pan-neuronal activity suppressing experiments. Unless otherwise noted, flies used were progeny from nSyb-LexA males crossed to female w1118. For activity suppressing experiments, injured flies were progeny from nSyb > Shibirets1 stably-expressing males crossed to female w1118.
High-speed video recording and video-assisted startle-induced climbing assay
High-speed video recording of head impacts was acquired using a Phantom Miro M310 high-speed camera controlled by a PC with Phantom Camera Control (PCC) software. Sequences recorded at either 3205 or 4106 frames per second were imported into Image J. Body orientation at impact was measured using the Angle tool.
Startle-induced climbing was assessed using a modified negative geotaxis assay. Flies were placed in vials containing 5% agar. Up to four vials were assayed at the same time, using a custom 3-D Polylactic Acid (PLA) printed rig. For each trial, the rig was lightly tamped three times, and fly movement was recorded using a Panasonic HC-V800 digital video recorder at 60 frames per second. Individual vials from each video were cropped, and the first 10 s were trimmed in Image J and underwent automated fly behavior tracking using id.tracker.ai. All testing took place between ZT 3 and ZT 8 (ZT, Zeitgeber time; lights are turned on at ZT 0 and turned off at ZT 12) and testing occurred between 20 and 22 °C under normal lighting conditions.
Automated fly behavior tracking using idtracker.ai
Automated fly behavior was performed using idtracker.ai, a deep-learning algorithm and software that permits individual tracking of flies. All videos were processed on a Google Cloud Compute Virtual Machine (VM) running a PyTorch Deep Learning VM Instance (c2-deeplearning-pytorch-1-2-cu100-20191005) equipped with an N1-Standard-16 (16 vCPUs, 60 GB memory) machine type, an NVIDIA Tesla T4 GPU, a 100 GB SSD disk and Intel Haswell CPU platform. Subsequent data analysis was performed using custom Matlab scripts.
Immunohistochemistry for detecting neurodegeneration
Whole flies were fixed for 3 h in 4% paraformaldehyde (PFA) in phosphate-buffered saline containing 0.5% Triton-X (PBS-T). The flies were rinsed 4 times for 15 min each with PBS-T and brains were subsequently dissected in PBS-T. Brains were permeabilized overnight in 0.5% PBST at 4 °C with nutation then blocked in 5% normal goat serum (NGS) in PBS-T for 90 min at room temperature with nutation. Brains were stained with DAPI (1:1000; Invitrogen D1306) (nuclear marker) and Alexa Fluor 594 (AF594) phalloidin (1:400, Invitrogen A12381), which binds to filamentous actin and stains the whole-brain parenchyma. Regions devoid of DAPI and phalloidin are considered vacuoles (Supplemental Fig. S1). Stained brains were rinsed 4 × 15 min with PBS-T, followed by one wash in PBS for 90 min and then mounted on glass slides within SecureSeal Imaging Spacers (Grace Bio-Labs, Bend, Oregon, USA) containing SlowFade Gold Antifade mounting medium (Life Technologies, Carlsbad, CA, USA S36937). Whole-brain imaging was performed using an Olympus FV1000MPE two-photon system equipped with a water immersion objective XLPLN25XWMP (working distance of 2 mm and N.A. of 1.05) to acquire 1 µm thick sections. Image analysis was performed using ImageJ (Fiji) software.
To demonstrate that vacuoles detected using this strategy correspond to neuropil loss, additional confirmatory staining was performed on a subset of brains for the post-synaptic marker with mouse monoclonal α-discs large 1 [1:50; DSHB 4F3] (Supplemental Fig. S1). The secondary antibody was AF-568 labeled goat anti-mouse Ig (1:400; Invitrogen A11031). Alexa Fluor 488 (AF488) phalloidin (1:400, Invitrogen A12379) replaced the use of AF594 phalloidin. Whole-brain imaging of 1 µm thick sections was performed using either an Olympus FV1000MPE two-photon system or a Nikon C2 laser-scanning confocal.
Neuronal activity luciferase reporter
To measure luciferase activity, representative groups of 2–4 OK107 > CaLexA-LUC sham and injured flies were quickly immobilized using CO2, decapitated and heads collected in 100µL 1 × Promega Glo Lysis Buffer (Promega #E2661), and 4–7 independent samples were collected for each treatment group. Fly heads were homogenized using an automated pestle motor mixer (Argos Cat. No. A0001) for 1 min at room temperature, then incubated at room temperature for 1 h, then centrifuged for 10 min at 13.5 k RPM. The supernatant was transferred to a new tube. For luciferase assays, 60 µL of each sample was mixed 1:1 with Steady-Glo Luciferase system (Promega #E2510) following the manufacturer’s protocols, and then added to a white-walled 96-well plate at room temperature and incubated in the dark for 10 min. Luminescence was measured using a BioTek Synergy HTX Multi-Mode Reader.
Data reporting and statistical analysis
No statistical methods were used to determine sample sizes but are consistent with sample sizes similar to those generally employed in the field51. Experimenters were not blinded as almost all data acquisition and analysis was automated. All flies in each vial were administered with the same treatment regimen. For each experiment, the experimental and control flies were collected, treated, and tested at the same time. A Mann–Whitney U test with Bonferroni or Holm correction for multiple comparisons was used for statistical analysis of behavioral data. All statistical analyses were performed using R (R v3.5, [rstatix]). P values are indicated as follows: ****P < 0.0001; ***P < 0.001; **P < 0.01; and *P < 0.05. For boxplots, lower and upper whiskers represent 1.5 interquartile range of the lower and upper quartiles, respectively; boxes indicate lower quartile, median, and upper quartile, from bottom to top. When all points are shown, whiskers represent range and boxes indicate lower quartile, median, and upper quartile, from bottom to top.
Development of a novel repetitive head impact Drosophila model
To investigate the long-term consequences of repetitive head trauma, we developed a novel repetitive head injury model using Drosophila that accurately and precisely delivers headfirst acceleration-deceleration-mediated head impacts (Fig. 1a). Multiple flies (10–15 flies at a time) are contained within a custom plastic injury vial designed to fit within our injury rig consisting of a cradle that is connected to a pulley system with a specific counterweight. To ensure consistency across injuries, each injury trial consists of pulling the cradle downward to the base of the injury rig, followed by lightly tamping the cradle three times for all the flies to fall to the bottom of the vial before releasing it for upward acceleration. When the cradle, which contains the injury vial with flies suddenly stops at the top, the momentum of the fruit flies continues to propel them upward, where they sustain headfirst impacts against the glass ceiling at the top of the vial (Fig. 1a, Supplemental Video S1). The light tamping is employed for two purposes: (1) to cause all the flies to fall to the bottom so they will travel the same distance before the head impact for consistent impact speed and (2) to allow the flies to orientate in a head-upward posture as part of their startle-induced negative geotactic climbing response. Indeed, our high-speed video recording revealed that many of the flies hit the top ceiling with their heads first, resulting in an impact angle of nearly 90 degrees (anterior–posterior body axis perpendicular to the impact surface, see Fig. 1a). This tailored approach improves upon an existing strategy that delivers traumatic injury to flies within a vial that is accelerated in a circular motion44, which causes the flies to undergo a tumbling motion, thereby prompting subsequent nonspecific impacts sustained to systemic regions of the body other than the head (Fig. 1b) and limiting the head-specific conclusions that can be drawn from this type of injury. With our current impact configuration, we determined using the high-speed video recording that each fly experienced an impact that involves ~ 1 ms of contact at a speed of ~ 4 m/s with the glass ceiling (Fig. 1a, arrows indicate immediately before and after contact between the fly and impact surface; asterisks indicate contact with impact surface). Immediately following headfirst impact, flies fell to the floor of the vial and exhibited a concussive-like behavioral response indicative of neurological injury (Fig. 1c, Supplemental Video S2) whose frequency increases with the number of successive impacts incurred; these behavioral signs include: temporary loss of consciousness and other uncoordinated behavioral responses (Supplemental Video S2). Importantly, flies sustain no gross morphological damage to the head or body following repetitive head impact exposure, indicative of a closed-head injury (Supplemental Fig. S2A). It should be noted that the floor of the vial is coated with a thin elastic silicone layer (2 mm) (SYLGARD, The Dow Chemical) that serves as the cushion to minimize any potential inadvertant damage to falling flies.
Acute recovery of climbing deficits following minimally lethal repetitive head impacts is sexually dimorphic
To emulate repetitive mild head injury exposure sustained across time, young adult (3 days post-eclosed) male and female flies were subjected to two sessions of repetitive impacts 24 h apart; each session consisting of 15 iterative impacts delivered 10 s apart (Fig. 2a). Repetitively impacted flies exhibited minimal (< 7%) acute mortality following both days of impacts (Fig. 2b), whereas a single head impact generated no acute death (Supplemental Fig. S2B). This degree of mortality is far less than the mortality (20–60%) seen in a commonly employed method used to deliver repetitive head trauma to flies44,52, indicating that our approach delivered a much milder insult (thus considered as “mild head trauma”). Following the injury, flies were rested for 1.5 h before functional recovery testing was performed. This length of recovery time enabled acute recovery from temporary uncoordinated and seizure-like behaviors seen shortly following injury48, and allowed flies to regain postural stability needed to perform the behavioral function assay. To measure acute behavioral deficits following repetitive head impacts, startle-induced climbing was assessed using the negative geotaxis assay (NGA)53,54,55,56, which is a widely used locomotor assay sensitive to age-related decline and neurodegeneration. This assay tests both vestibulomotor and sensorimotor functions which are commonly assessed in traditional mammalian TBI models57,58,59. Flies were placed in plastic vials containing 2 mL of 5% agar at the bottom and subjected to gentle tamping to induce a startle response. Videos were analyzed using an automated python-based tracking software, idtracker.ai60,61, to measure cumulative climbing distance (slope), total (final) and vertical distance traversed in a 10 s span of time following the startle stimulus (Supplemental Video S3). Testing was performed 1.5 h after the first and second sessions of repetitive impacts (“1.5 h” and “25.5 h” with respect to the initial injury), as well as 24 h after each session to assess longer recovery (“24 h” and “48 h” with respect to the initial injury). While injured males showed an initial deficit in climbing after each session that resolved 24 h later, female flies exhibited a progressive climbing deficit that was further exacerbated following the second session of impacts (Fig. 2c,d, Supplemental Fig. S3). 24 h after the second session, a robust difference in climbing behavior was seen between injured sexes, with injured female flies showing a 30% reduction in climbing whereas injured males performed similar to their sham counterparts (Fig. 2e).
Lifelong deficits after early exposure to repetitive mild head impacts
One key advantage of our Drosophila model of mild head trauma is that it enables the monitoring and examination of long-term effects on lifespan and brain structure and function in relatively large cohorts. We thus continued to routinely examine flies following repetitive mild head impacts over their lifespan. We first measured the mortality and found that repetitive head impact exposure resulted in a shortened overall lifespan that was more prominent in female flies (Fig. 3a,b). To determine the effect of repetitive head injury exposure on long-term behavioral function, startle-induced climbing performance was routinely assessed until 98 days (14 weeks) post-injury. Flies subjected to repetitive head injury exposure exhibited long-term climbing deficits that were more profound in female than male flies (Fig. 3c–e, Supplemental Fig. S4). Significant deficits in climbing performance of injured female flies were consistently observed up to 70 days post injury (Fig. 3c,d). During this time period, injured female flies exhibited a greater reduction in climbing ability compared to injured males (Fig. 3e). By 84 days post-injury, female flies from the sham and injury groups exhibited no apparent difference in their climbing performance, which is likely attributed to the severely reduced baseline performance due to aging. On the other hand, male files appear to perform better at these later ages (84- and 98-days), as such, a small difference between injured and sham male flies in climbing performance existed up to 98 days post-injury (Fig. 3c,d, Supplemental Fig. S4). Together, this data demonstrated that early exposure to repetitive mild head trauma disrupts motor functions that lasts over a long period of time and disproportionally impacts female flies.
Repetitive head impacts exacerbate age-related brain degeneration
To examine brain pathology related to repetitive head injury exposure, whole-brain gross neurodegeneration was longitudinally assessed by measuring vacuolization; a commonly used measure of neurodegeneration in Drosophila40,62. To measure vacuolization, whole-brains were stained with phalloidin to detect actin-rich neuropil and DAPI to detect nuclei, and imaged using two-photon microscopy. Regions devoid of both DAPI and phalloidin signals were characterized as vacuoles42. Brains from flies subjected to repetitive impacts were processed for neurodegeneration acutely (1.5 h) and chronically (5 weeks) post-injury. Although minimal to no vacuolization existed at the early time point across sexes and injury groups (Supplemental Fig. S5), aged brains exhibited a far greater degree of vacuolization, as measured by the number and area of vacuoles per brain (Fig. 4). Both female and male flies subjected to repetitive head impacts resulted in an increase in neurodegeneration five weeks post-injury relative to sham (Fig. 4a–d), seen as an increase in the overall number of vacuoles per brain (Fig. 4e) and overall area of vacuoles per brain (Fig. 4f).
Elevated brain activity by repetitive mild head impacts and the protective effects by acute suppression of neuronal activity are sex-dependent
We next began to explore the mechanisms underlying the development of long-term behavioral and brain dysfunction after repetitive mild head impacts. Emerging evidence indicates that neuronal hyperexcitability plays an important role in a number of neurodegenerative disorders63. Neuronal hyperexcitability has been examined in moderate to severe TBI16,17, but its existence in mild TBI remains poorly understood. We thus investigated if repetitive mild head trauma exposure in Drosophila elicits neuronal activity in vivo. To do so, we measured neuronal activity using a non-invasive in vivo luciferase-based transcriptional indicator of calcium signaling, CaLexA-Luciferase (CaLexA-LUC)49,64 (Calcium-dependent nuclear import of LexA); a Nuclear factor of activated T-cells (NFAT)-LexA chimera whose transcriptional activity is based on the Ca2+-regulated dephosphorylation and nuclear translocation of NFAT which then drives luciferase expression. Pan-neuronal expression of UAS-CaLexA-LUC using the neuronal synaptobrevin-GAL4 (nSyb-GAL4) is weak and sparse51, and in our hands, results in sick and sluggish appearing flies (data not shown). Instead, we measured neuronal activity in an essential midbrain structure, the mushroom body65, using the robust mushroom body driver to express CaLexA-LUC (OK107 > CaLexA-LUC). The mushroom body contains roughly 2% of the total fly brain neurons65 and features a dense organization of projection neurons that communicate with various regions of the fly brain, making it a center for high-level integration of functions related to learning/memory65 and startle-induced climbing66. OK107 > CaLexA-LUC flies were subjected to repetitive impacts (1 session of 30 impacts) and collected for fly head lysate preparation 1.5 h following injury. Bioluminescence (luciferase activity) was measured from collected fly head lysates. Injured female flies exhibited a 20% increase in measured neuronal activity relative to their sham female counterparts, whereas no significant difference was seen between injured and sham male flies (Fig. 5a).
We then took a tailored approach to conditionally suppress neuronal activity at the time of injury, using the temperature sensitive dynamin homologue mutant, shibirets1 (shits1)50,67,68 expressed pan-neuronally (nSyb > shits1). Pan-neuronal expression of shits1 enables conditional suppression of synaptic activity by halting synaptic vesicle release, via interruption of the readily releasable pool of synaptic vesicles, thereby inducing a reversible state of flaccid paralysis50,67,68. Conditional suppression of synaptic activity occurs rapidly when exposed to the non-permissive temperature threshold of 30 °C, which is initially achieved through transfer to a pre-warmed vial and maintained via exogenous heat delivered by a heat lamp.
Control flies expressing either pan-neuronal LexA only (nSyb-LexA) or pan-neuronal shibirets1 (nSyb > shits) flies were injured during two sessions of 15 impacts delivered 24 h apart. During each injury session, flies were subjected to the non-permissive temperature for only the extent of the injury induction period (~ 2.5 min long) (Fig. 5b). Suppression of neuronal activity at the time of injury nearly abolished the acute mortality found in both sexes of injured nSyb-LexA flies and restored normal female lifespan (Fig. 5c). Most interestingly, suppression of neuronal activity at the time of injury restored relative acute female climbing performance compared to nSyb-LexA injured performance, whereas injured nSyb > shits1 males showed no significant improvement compared to injured nSyb-LexA (Fig. 5d; Supplemental Fig. S6). Moreover, long-term climbing performance of injured nSyb > shits1 females better resembled their sham nSyb > shits1 counterparts compared to injured nSyb-LexA flies (Fig. 5e; Supplemental Fig. S7). This finding was most prominent during Days 42–70 post-injury. Interestingly, the long-term relative performance of injured male nSyb > shits1 flies appeared no different than injured nSyb-LexA flies, which may be due to the milder initial climbing deficit seen in injured males (Fig. 3).
We next examined if blocking acute activity at the time of injury is protective against long-term neurodegeneration following repetitive head impacts. Similarly, repetitive head impacts were delivered to nSyb > shits1 flies at the non-permissive temperature and injured nSyb > shits1 flies were processed using the same methods shown in Fig. 4 for vacuole assessment following the aforementioned acute-silencing regimen. Acute silencing of activity at the time of injury was found to substantially reduce the number and size of vacuoles in female brains, while no obvious reduction in injury-induced vacuole formation was found in injured male brains from nSyb > shits1 compared to nSyb-LexA (Fig. 6). Together with the mortality and climbing data, this data suggests that acute aberrant neuronal activity elicited by repetitive head trauma may potentiate long-lasting dysfunction that preferentially affects female flies. In accordance with this finding, blocking acute activity through the expression of the dominant negative transgene, shibirets1 provides long-term neuroprotection against repetitive injuries that preferentially benefits females.
An emerging body of evidence demonstrates that a past history of repetitive mild head trauma increases the risk for developing cognitive and motor impairment, and brain degeneration later in life5,6. However, it remains unclear how the early exposure to mild head trauma leads to the development of long-term neurological dysfunction. This is in part due to the challenges using existing animal models for lifelong examination and interrogation of the detrimental effects after injury. In this study, we developed a Drosophila head impact system to investigate the long-term detrimental effects of mild repetitive head trauma and their underlying mechanisms. Our data show that repetitive mild physical impacts delivered to the adult fly head result in acute concussion-like responses and impairments in startle-induced climbing behavior. Importantly, when monitored over an extended period of time (throughout the entire lifespan), the early repetitive head trauma was found to shorten lifespan and elicit a decline in behavior, particularly in female flies. Whole-brain imaging also revealed increased brain degeneration in flies that received early repetitive head trauma. Finally, we provided evidence that neuronal activity plays a critical role in mild head trauma-induced long-term deficits in behavior and brain pathology within female flies.
While fruit flies are anatomically different from human, it has become clear that Drosophila is an excellent model organism to investigate the molecular, cellular, and genetic mechanisms underlying a wide range of human disorders. For example, the use of Drosophila has led to the discovery of novel genes and mechanisms of neurodegeneration36,69,70,71,72,73, including those involved in axonal transection-mediated degeneration, that have been validated by subsequent murine74,75,76 and human studies77. Existing head trauma models have also demonstrated conserved neuropathology in flies that recapitulates human aspects of head trauma8, including frank neurodegeneration48, and other cellular pathologies implicated in chronic traumatic encephalopathy, such as hyperphosphorylation of tau45 and abnormal accumulation of TDP-4378. The findings from our study not only support the use of Drosophila as a model system to study the long-term brain degeneration and dysfunction secondary to environmental insults, but also provide crucial insight into the underlying mechanisms involving excitatory neuronal activity in the development of brain deficits induced by head trauma. Our finding that silencing neuronal activity largely abolishes the long-term detrimental effects on fly behavior and brain pathology is consistent with the emerging view on the involvement of excitotoxicity in a number of neurodegenerative disorders63 including TBI79,80,81. Lastly, our findings also suggest that lifelong injury outcomes are exacerbated in the female flies compared to male flies.
Our newly developed Drosophila head impact model possesses several unique features that distinguish it from other systems. First, the physical impacts are delivered mostly to the heads of awake and unrestrained flies. The headfirst collision of flies to the impact ceiling is achieved in part through the upward body orientation at the start of acceleration due to the innate negative geotactic escape response during which flies orient headfirst against the force of gravity when startled. The aerodynamic body shape of the flies is also believed to contribute to the headfirst impact orientation as we observed mostly headfirst impacts with flies in a coma (data not shown). Second, the headfirst impacts are delivered to a large cohort of flies (10–15 flies at a time), thus increasing the efficiency for investigating the effects on large populations that are essential for analyzing genetic variations and long-term age-dependent changes, the latter of which is made possible by the relatively short overall lifespan of fruit flies. This, together with our non-invasive automated behavioral testing paradigm, is amenable to future high-throughput screening for genetic and environmental modifiers. Third, injury severity, or the impact force sustained by the fly head can be specifically modified by adjusting the hardness of the impact surface. For example, our current glass impact surface, which is a circular glass coverslip, can be replaced with a surface material of different hardness, such as plastic or Styrofoam, which can provide a specific degree of buffering for mimicking the padding of helmets in contact sports. Injury severity can also be adjusted within our system by using different counterweights and heights within the pulley system, resulting in a change in velocity at impact. Therefore, our head impact system has the potential to be utilized in a wide range of studies concerning head trauma that are focused on behavioral, structural, and functional consequences using adult flies of different ages and genetic backgrounds, helping to better understand the risk factors in the development of neurodegeneration and long-term dysfunction after head trauma.
While most affected individuals appear to recover from mild head trauma, the risk for developing long-term deficits in brain function and structure has been documented5. One interesting finding in our study is that female flies were more affected by repetitive head impacts than males. This was seen behaviorally, as a greater reduction in climbing ability relative to sham injured flies, as well as a shortened overall lifespan. The greater persistent functional deficit found in female flies following injury parallels human data from the Transforming Research and Clinical Knowledge in Traumatic Brain Injury (TRACK-TBI) study in which the female sex was associated with decreased six-month functional outcome measured using the Glasgow Outcome Scale-Extended (GOSE)82. A recent cross-sectional human study revealed that females were more likely to report a less favorable health-related quality of life (HRQoL) during the chronic stage of TBI (10 years post-injury)83. Additional evidence demonstrates that young female athletes may take longer to become symptom free following sports-related concussion84. Taken together, this demonstrates sex differences following recovery from TBI and substantiates the importance of using both sexes in preclinical animal models. Interestingly, sex-dependent differences in function (climbing behavior) in fly head injury models has only been examined once prior, in which no differences between sexes were revealed43. However, flies were only measured for 72 h during the post-injury period, and the method for measuring behavior was done using the traditional approach to measure startle-induced climbing performance53,54. To provide greater sensitivity to potential subtle differences in climbing behavior, we used idtracker.ai60, an automated deep-learning tracking algorithm that enables measurement of individual fly performance. Climbing function was measured until 98 days post-injury, which accounted for most of the overall lifespan for flies reared at 18 °C (~ 150 day median survival).
At this moment, the underlying mechanism for the greater vulnerability to mild head trauma for female flies remains unclear. In humans, females are more likely to report mild TBI85, but several biological factors have been proposed to account for sex-dependent differences. For example, gender differences in head-neck anatomy in human can result in greater head acceleration (angular acceleration and displacement) in females compared to males86,87, which may elicit a greater force acted upon the head and thus increase the injury risk found in females87. In Drosophila, female flies are known to have a relatively larger body size compared to males88,89, which may incur a greater impact force and account for worse outcomes following injury. It is also possible that sex-dependent differences in neuroanatomy and gene expression may contribute to the greater vulnerability of females to head injury. To start addressing this possibility, we have performed a preliminary study in which the female specific sex determination gene transformer (tra)89 was expressed in the post-mitotic neurons of the male flies using nSyb-GAL490. When these flies were subjected to two sessions of repetitive impacts (24 h apart; each session = 15 iterative impacts delivered 10 s apart), we found that males expressing the female-specific transformer (nSyb > Tra) performed similarly to their injured nSyb-GAL4 counterparts (Supplemental Fig. S8). This finding suggests that neuroanatomical differences, but not female-specific gene expression in neurons may be responsible for the increased vulnerability to injury seen in female flies. We also noted that male flies expressing transformer (nSyb > Tra) appear to be larger in size comparing to the control (nSy-GAL4 only). The lack of difference in climbing responses after repetitive head impacts between these two groups also argue against the size difference as a major factor contributing to the female vulnerability in head trauma. Clearly, further investigation is needed to fully elucidate the molecular and genetic mechanisms underlying the sexually dimorphic responses to head injury.
Neuroanatomical differences have been suggested to contribute to sexually dimorphic vulnerability to injury in vitro91. In response to mechanical trauma, sudden stretching of the axon can increase membrane permeability, resulting in the temporary loss of ionic homeostasis, an influx of cations and excessive excitatory neurotransmitter release, and subsequent excitotoxicity, metabolic dysfunction, and cell death15,16,17,18,19. Cultured neurons from female human and murine sources contain axons with fewer microtubules per axon, resulting in a thinner axon diameter compared to males91, making it potentially more vulnerable to trauma. Moreover, in response to injury using a cell stretch injury model, female axons exhibited a greater acute influx of calcium compared to males91, which may explain the finding of more persistent deficits in hippocampal synaptic plasticity following mild TBI seen in preclinical data from female rats92. Our study provides corresponding in vivo data demonstrating that repetitive injury elicits acute neuronal activity within the injured female fly brain. Although this surge of excitation is thought to be short-lived, on the scale of minutes to hours93,94, this action may potentiate long-lasting effects on synaptic plasticity and neuronal function and affect the brain’s vulnerability to further injury, however this theory remains untested in part due to the lack of animal models for long-term examination.
Here in this study, we were able to target neuronal activity, specifically neurotransmitter release, at the time of injury using the transgenic temperature-sensitive shibirets1 mutant fly line as a tool to conditionally suppress whole-brain neuronal activity and monitor mortality, lifelong functional deficits, and brain degeneration. Our data provides the first evidence that silencing neuronal activity at the time of injury was able to largely mitigate the long-term detrimental effects of mild repetitive brain trauma in female flies. Together, this supports a mechanism involving synaptic plasticity and neuronal excitability related to chronic trauma-induced degeneration. While the protective mechanism of blocking activity remains unclear, it is likely associated with the downstream mechanisms of hyperexcitability following mechanical injury. The surge of neuronal activity can result in an influx of calcium, and subsequent activation of proteases, caspases, and mitochondrial dysfunction95, which eventually contribute towards cell death and degeneration. Blocking the activity surge during mechanical insults could potentially inhibit the excitotoxicity that would otherwise trigger the long-term cascades related to neurodegeneration and long-term dysfunction. Future work using our system can assess the potential benefit of silencing activity at various timepoints following repetitive injuries to determine the long-term therapeutic window of active rest, which is a commonly prescribed treatment following head injury. Additional work will also longitudinally examine how early repetitive head impact exposure affects neuronal excitability later in life, especially given that increased neuronal excitability is associated with brain aging96, for which injury exposure may accelerate.
Although blocking activity seemed to preferentially benefit injured females to a greater extent than injured males, this may be related to the timing and duration of the activity suppression. Within our current paradigm, neuronal activity suppression was limited to the time of the injury exposure (~ 2.5 min), after which flies were quickly returned to the permissive temperature for the remainder of their lives. Additional strategies could be used within our current system that provide chronic suppression of changes in hyperexcitability using glial cells involved in excitatory neurotransmitter recycling by specifically targeting excitatory neurotransmitter transporters97,98,99. The inability to properly regulate excitability may be related to the loss of excitatory neurotransmitter buffering capacity in glial cells, primarily astrocytes, which have been shown to be perturbed in severe isolated scenarios of head trauma100,101. While this remains to be seen in repetitive mild head trauma exposure, decreased buffering capacity may potentiate chronic changes in hyperexcitability that then result in eventual neuronal degeneration. Interestingly, the early stages of Alzheimer’s disease may involve abnormal changes in glutamatergic buffering, which results in persistent excessive neuronal activation, excitotoxicity and eventual cell death102,103. Activity-dependent changes related to repetitive exposure to trauma may represent an early mechanism that potentiates AD, as well as other neurodegenerative diseases. Additional studies using our tractable injury model can also examine the role of hyperexcitability towards the formation of abnormal protein deposition seen in AD and CTE, including hyperphosphorylated tau and TDP-43 inclusions8,11,104.
This work utilizes a novel Drosophila head impact model to investigate how early exposure to repetitive mild head trauma results in long-term brain dysfunction and degeneration. We find that exposure to repetitive trauma resulted in lifelong brain dysfunction and degeneration that is further exacerbated in female flies. We also uncovered a novel activity-dependent mechanism underlying head trauma-induced long-term brain deficits. The finding that silencing neuronal activity during head impacts can effectively mitigate the development of long-term deficits suggests it as a potential therapeutic target for treating chronic sequalae of repetitive mild head trauma exposure. The basis of this work calls to question whether treating milder, potentially unassuming injuries, should receive greater attention as a means to thwart long-term complications. Understanding the natural course and lifelong implications of head trauma exposure is critically important for developing long-term neuroprotective strategies. We will continue to use our tractable fly model to investigate genetic and environmental factors that affect neurodegeneration secondary to repetitive head trauma exposure and provide insight into the fundamental mechanisms that lead to the progression of lifelong neurological dysfunction.
Experimental tools and data are available from the corresponding authors.
Analysis of variance
Calcium-dependent nuclear import of LexA
Central processing unit
Graphics processing unit
Phosphate buffered saline
- Shits1 :
Shibire temperature-sensitive 1
Solid state drive
Traumatic brain injury
Upstream activator sequence
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We thank Drs. Janet Alder, Smita Thakker-Varia and Michael Sayegh for their comments on the manuscript. We also thank Dr. Brian Robinson and Chris Rounds for their technical assistance with Drosophila handling, and Dr. Lauren Stewart at Georgia Institute of Technology for her help with high-speed video recording. Corey Zheng at Georgia Institute of Technology helped with the design and construction of the Pulley impact system as well as the 3-D printing of the impact cradle. Thank you to Teri Ngo (Rubin Lab) and Dr. Kate Abruzzi (Rosbash Lab) for providing fly stocks. This research project would not have taken shape without stimulating discussions with Drs. Dorothy Lerit and Victor Faundez, and other colleagues within the Department of Cell Biology at Emory University.
This research project was supported in part by research grants from the National Institutes of Health to JQZ (GM083889, R01MH104632) and to KHM (MH107305). This research was also supported in part by Google Cloud’s Academic Research Credits Program to JAB.
The authors declare no competing interests.
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Behnke, J.A., Ye, C., Setty, A. et al. Repetitive mild head trauma induces activity mediated lifelong brain deficits in a novel Drosophila model. Sci Rep 11, 9738 (2021). https://doi.org/10.1038/s41598-021-89121-7