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Walker, A. B.

Publications and source records attributed to Walker, A. B..

4 recordsLinked to original sources

Bacterial-driven development is mediated by Calcium-Dependent Intrinsic Apoptosis in the Squid-Vibrio Symbiosis

The presence of beneficial microbes serves as a post-embryonic developmental cue in a wide array of metazoan species. However, the mechanisms through which mutualistic bacteria induce developmental processes such as apoptosis are poorly understood. A leading model system utilized to study bacteria-induced developmental apoptosis is the Hawaiian bobtail squid, Euprymna scolopes, whose bacterial symbiont Vibrio fischeri induces several developmental events upon colonization of the squids light organ. Upon hatching the light organ possesses ciliated epithelial fields (CEFs) and appendages that facilitate the collection of V. fischeri from the ambient seawater for symbiont colonization of the internal crypt spaces. To better understand the molecular pathways underpinning bacterial-induced development occurring in these appendages, we isolated appendages from hatchling (0-1h) and aposymbiotic and symbiotic E. scolopes light organs (18h) for RNA sequencing. Our analysis of this transcriptomic dataset indicated that symbiotic appendages undergo intrinsic apoptosis in response to excessive cytosolic calcium. Further experiments found that symbiotic appendages exhibited increased cytosolic calcium and mitochondrial membrane potential overload relative to their aposymbiotic counterparts. In comparing our appendage specific gene expression to previously published whole light organ transcriptomic dataset, we identified increased presence of apoptosis inducing factor (AIF) and decreased expression of transcripts related to protein folding in the appendages as potential mechanisms of apoptotic signal specificity to the CEF. Together, these data suggest a central role of cytosolic calcium in the developmental apoptotic signaling induced by V. fischeri colonization of the E. scolopes light organ. ImportanceBacterial cues are known to induce post-embryonic animal development, but the mechanisms mediating crosstalk between bacterial product recognition and developmental dynamics require further study. Because of its binary nature and clear developmental phenotypes, the Euprymna scolopes- Vibrio fischeri system is an excellent model for symbiont-induced development. Here, we characterize the symbiont-induced apoptotic signaling that mediates the loss of V. fischeri recruitment structures in the E. scolopes light organ following colonization. Transcriptomic changes in colonized light organs and subsequent microscopy-based experiments support that acquisition of V. fischeri induces loss of the ciliated symbiont recruitment structures in juvenile light organs via intrinsic apoptotic signaling initiated by excess cytosolic calcium. This work advances our understanding of how mutualistic bacterial cues initiate signal transduction to induce developmental programming and may serve as a foundation upon which we can begin to disentangle the ways in which more diverse and complex microbial communities influence post-embryonic development.

developmental biology↗

The Neuroanatomy of the Hawaiian Bobtail Squid Juvenile Bacterial Light Organ

BackgroundRecent studies have shown that symbiotic bacteria can have drastic effects on host neurobiology, but few simple, accessible models currently exist in which to study these interactions. Hawaiian bobtail squid (Euprymna scolopes) participate in a binary symbiosis with the bacterium Vibrio fischeri, a population of which resides in a specialized hindgut-derived organ called the light organ. Upon colonization by V. fischeri, the light organ undergoes transcriptional changes that suggest neurons are among the cell types impacted by the initiation of symbiosis, but the nascent light organs innervation has remained uncharacterized. ResultsThe light organ-associated nervous system (LONS) in hatchling E. scolopes is a remarkably complex segment of the peripheral nervous system. The LONS is largely plexiform and originates from two primary nerves connected by a local commissure. The abundance of synapsin-like immunoreactivity indicates that the lobe plexus is highly interconnected. We also highlight a small number of serotonin-like immunoreactive neurites innervating the anterior appendages that are poised to be directly impacted by symbiont-driven post-embryonic development. Finally, we present evidence that a limited but morphologically diverse population of neurons reside within the light organ and are often located near internal symbiont-interacting structures. ConclusionOur results show that the LONS is structurally and molecularly complex and exhibits traits characteristic of an immature nervous system, suggesting that it may undergo substantial post-embryonic refinement. This initial characterization of the LONS provides a foundation from which to investigate how beneficial bacterial symbionts affect host peripheral neurobiology in a tractable model system.

neuroscience↗

Estradiol treatment enhances neurovascular coupling independent of metabolic health status in a mouse model of menopause

The loss of ovarian estrogen during the menopause transition has been identified as a risk factor for increased cardiometabolic and neurovascular dysfunction, age-related cognitive decline, and Alzheimers disease. A wealth of studies using rodent models of menopause have highlighted the cardio- and neuroprotective effects of 17{beta}-estradiol (E2) treatment when administered within a critical period, though these have yet to be successfully translated to human populations in clinical trials of hormone therapy. A proposed explanation for this mismatch in results is the "healthy cell bias," where estrogen is only beneficial when initiated in physiologically intact systems. Our study investigates whether pre-existing metabolic dysfunction attenuates the effects of E2 on neurovascular coupling (NVC) in a rodent model of menopause. Female mice were fed a high-fat diet (HFD) or control diet (CD) for 11 weeks to induce metabolic dysfunction, followed by ovariectomy (OVX) and subsequent E2 or vehicle (Veh) treatment. NVC was assessed in awake mice using two-photon laser scanning microscopy of penetrating arterioles (PAs) in the somatosensory cortex, barrel field. Mice developed glucose intolerance and increased adiposity yet displayed intact NVC following 11 weeks of HFD exposure. Following ovariectomy, E2 treatment enhanced NVC responses regardless of diet. Interestingly, in HFD-fed mice, E2 appeared to reduce basal PA diameter relative to Veh, suggesting health status-specific mechanisms of action. These results indicate that PAs retain functional sensitivity to estrogen treatment in the face of metabolic impairment, which has implications for the use of hormone therapy in women that arrive at the menopause transition with varied pre-existing cardiometabolic disorders.

neuroscience↗

The benefits of estradiol on cognitive aging in rats are independent from its effects on cardiometabolic health

Research in preclinical models of menopause indicates that exogenously administered estrogens positively impact cognitive aging. However, clinical evidence indicates that the effects of estrogen therapy on cognition are inconsistent and may be modulated by pre-existing cardiometabolic conditions. The extent to which cardiometabolic health affects the cognitive outcomes of estrogen therapy remains unclear. This study aimed to determine whether variations in cardiometabolic health, both prior to and resulting from different estradiol treatment regimens, are related to the ability of estradiol to improve the cognitive aging trajectory in ovariectomized Long-Evans rats. Cognitive function and health status were assessed at 10 months of age after which rats were ovariectomized and administered vehicle or various estradiol treatments. Rats were assessed again at 18 (middle age) and 22 (old age) months. Cognition was evaluated using a spatial memory radial-maze task. Health status was determined through body composition (dual-energy X-ray absorptiometry), glucose tolerance testing, and blood pressure (tail-cuff plethysmography). Results demonstrated that both continuous ongoing estradiol treatment and a previous 40-day estradiol exposure (terminated long before testing) significantly improved the cognitive aging trajectory from middle to old age. However, only continuous estradiol treatment had positive impacts on health measures; previous estradiol treatment provided no benefits to aging cardiometabolic systems. In contrast, a delayed estradiol treatment (initiated months after ovariectomy) provided no benefits for cognition but provided health benefits. Results indicated that estradiol impacts on cognition in healthy aging rats are separate from and not secondary to its effects on cardiometabolic health.

animal behavior and cognition↗