Lianna obtained her Ph.D. in Cell and Developmental Biology in Dr. Elizabeth Rideout’s lab at the University of British Columbia in 2021 where she studied the sex-specific regulation of fat metabolism using Drosophila as a model system. Lianna is bringing her expertise on sex differences and fat metabolism to the Svensson lab where she is interested in understanding in discovering secreted metabolic effectors that regulate male-female differences in energy metabolism and the development of metabolic disease
Honors & Awards
Larry Sandler Memorial Award, Genetics Society of America (2022-2023)
Elizabeth Young New Investigator Award, Organization for the Study of Sex Differences (2021-2022)
Laura G. Jasch Memorial Prize, University of British Columbia (2021-2022)
Canadian Institutes of Health Research Gold Award of Excellence, Canadian Institutes of Health Research (2020-2021)
Canadian Institutes of Health Research Sex & Gender Science Chair in Genetics Conference Award, Canadian Institutes of Health Research (2020-2021)
Gairdner Student Award, Canadian Institutes of Health Research (2020-2021)
Lindau Scholar Award, Canadian Institutes of Health Research (2020-2021)
University of British Columbia 1-Year CELL Fellowship, University of British Columbia (2020-2021)
British Columbia Graduate Scholarship, Government of British Columbia (2019-2020)
Raymond A. Pederson Prize in Physiology, University of British Columbia (2018-2019)
Boards, Advisory Committees, Professional Organizations
Member, Genetics Society of America (2020 - Present)
Member, University of British Columbia - Women's Health Research Cluster (2021 - Present)
PhD, The University of British Columbia, Cell and Developmental Biology (2021)
BSc, McMaster University, Honours Biology & Psychology (2016)
Katrin Svensson, Postdoctoral Faculty Sponsor
Protocol for invivo measurement of basal and insulin-stimulated glucose uptake in mouse tissues.
2023; 4 (2): 102179
Here, we present an invivo protocol for measuring basal and insulin-stimulated glucose uptake in tissues from mice. We describe steps for administering 2-deoxy-D-[1,2-3H]glucose in the presence or absence of insulin via intraperitoneal injections. We then detail tissue collection, tissue processing to measure 3H counts on a scintillation counter, and data interpretation. This protocol can be applied to other glucoregulatory hormones, genetic mouse models, and other species. For complete details on the use and execution of this protocol, please refer to Jiang etal. (2021).1.
View details for DOI 10.1016/j.xpro.2023.102179
View details for PubMedID 36933224
A low sugar diet enhances Drosophila body size in males and females via sex-specific mechanisms.
Development (Cambridge, England)
In Drosophila, changes to dietary protein elicit different body size responses between the sexes. Whether these differential body size effects extend to other macronutrients remains unclear. Here, we show that lowering dietary sugar (0S diet) enhanced body size in male and female larvae. Despite an equivalent phenotypic effect between the sexes, we detected sex-specific changes to signaling pathways, transcription, and whole-body glycogen and protein. In males, the low sugar diet augmented insulin/insulin-like growth factor signaling pathway (IIS) activity by increasing insulin sensitivity, where increased IIS was required for male metabolic and body size responses in 0S. In females reared on low sugar, IIS activity and insulin sensitivity were unaffected, and IIS function did not fully account for metabolic and body size responses. Instead, we identified a female-biased requirement for the target of rapamycin pathway in regulating metabolic and body size responses. Together, our data suggest the mechanisms underlying the low sugar-induced increase in body size are not fully shared between the sexes, highlighting the importance of including males and females in larval studies even when similar phenotypic outcomes are observed.
View details for DOI 10.1242/dev.200491
View details for PubMedID 35195254
Sex determination gene transformer regulates the male-female difference in Drosophila fat storage via the adipokinetic hormone pathway
Sex differences in whole-body fat storage exist in many species. For example, Drosophila females store more fat than males. Yet, the mechanisms underlying this sex difference in fat storage remain incompletely understood. Here, we identify a key role for sex determination gene transformer (tra) in regulating the male-female difference in fat storage. Normally, a functional Tra protein is present only in females, where it promotes female sexual development. We show that loss of Tra in females reduced whole-body fat storage, whereas gain of Tra in males augmented fat storage. Tra's role in promoting fat storage was largely due to its function in neurons, specifically the Adipokinetic hormone (Akh)-producing cells (APCs). Our analysis of Akh pathway regulation revealed a male bias in APC activity and Akh pathway function, where this sex-biased regulation influenced the sex difference in fat storage by limiting triglyceride accumulation in males. Importantly, Tra loss in females increased Akh pathway activity, and genetically manipulating the Akh pathway rescued Tra-dependent effects on fat storage. This identifies sex-specific regulation of Akh as one mechanism underlying the male-female difference in whole-body triglyceride levels, and provides important insight into the conserved mechanisms underlying sexual dimorphism in whole-body fat storage.
View details for DOI 10.7554/eLife.72350.sa2
View details for Web of Science ID 000720132300001
View details for PubMedID 34672260
View details for PubMedCentralID PMC8594944
Female-biased upregulation of insulin pathway activity mediates the sex difference in Drosophila body size plasticity
Nutrient-dependent body size plasticity differs between the sexes in most species, including mammals. Previous work in Drosophila showed that body size plasticity was higher in females, yet the mechanisms underlying increased female body size plasticity remain unclear. Here, we discover that a protein-rich diet augments body size in females and not males because of a female-biased increase in activity of the conserved insulin/insulin-like growth factor signaling pathway (IIS). This sex-biased upregulation of IIS activity was triggered by a diet-induced increase in stunted mRNA in females, and required Drosophila insulin-like peptide 2, illuminating new sex-specific roles for these genes. Importantly, we show that sex determination gene transformer promotes the diet-induced increase in stunted mRNA via transcriptional coactivator Spargel to regulate the male-female difference in body size plasticity. Together, these findings provide vital insight into conserved mechanisms underlying the sex difference in nutrient-dependent body size plasticity.
View details for DOI 10.7554/eLife.58341
View details for Web of Science ID 000618526800001
View details for PubMedID 33448263
View details for PubMedCentralID PMC7864645
A role for triglyceride lipase brummer in the regulation of sex differences in Drosophila fat storage and breakdown
2020; 18 (1): e3000595
Triglycerides are the major form of stored fat in all animals. One important determinant of whole-body fat storage is whether an animal is male or female. Here, we use Drosophila, an established model for studies on triglyceride metabolism, to gain insight into the genes and physiological mechanisms that contribute to sex differences in fat storage. Our analysis of triglyceride storage and breakdown in both sexes identified a role for triglyceride lipase brummer (bmm) in the regulation of sex differences in triglyceride homeostasis. Normally, male flies have higher levels of bmm mRNA both under normal culture conditions and in response to starvation, a lipolytic stimulus. We find that loss of bmm largely eliminates the sex difference in triglyceride storage and abolishes the sex difference in triglyceride breakdown via strongly male-biased effects. Although we show that bmm function in the fat body affects whole-body triglyceride levels in both sexes, in males, we identify an additional role for bmm function in the somatic cells of the gonad and in neurons in the regulation of whole-body triglyceride homeostasis. Furthermore, we demonstrate that lipid droplets are normally present in both the somatic cells of the male gonad and in neurons, revealing a previously unrecognized role for bmm function, and possibly lipid droplets, in these cell types in the regulation of whole-body triglyceride homeostasis. Taken together, our data reveal a role for bmm function in the somatic cells of the gonad and in neurons in the regulation of male-female differences in fat storage and breakdown and identify bmm as a link between the regulation of triglyceride homeostasis and biological sex.
View details for DOI 10.1371/journal.pbio.3000595
View details for Web of Science ID 000510743800011
View details for PubMedID 31961851
View details for PubMedCentralID PMC6994176