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Jacob Kallenbach awarded a Wilmot Cancer Institute predoctoral fellowship

Friday, June 12, 2020

Jacob Kallenbach

Jacob Kallenbach

Congratulations to PhD Candidate Jacob Kallenbach (Chakkalakal Lab), who was awarded a Wilmot Cancer Institute predoctoral fellowship to support his proposal on "Targeting CCR2 to Mitigate the Late Effects of Juvenile Radiation-Induced Skeletal Muscle Decline." 

He will investigate how adult survivors of childhood cancers are at an increased risk of diminished physiological musculoskeletal function, which is intricately connected to a survivor's quality of life. Jacob will exploit his lab's preclinical mouse model to study the early and late effects of juvenile radiation therapy, which comprises >50% of cancer therapies, on skeletal muscle tissues. The data from his study will be used to describe an inflammatory-mediated C-C chemokine receptor 2 (Ccr2) mechanism, where its inhibition could augment the functional quality of life of childhood cancer survivors.

The Wilmot Predoctoral Cancer Research Fellowship provides two years of support for Ph.D. or M.D./Ph.D. candidates under the mentorship of a Wilmot Cancer Institute member. The goal of the program is to enable emerging scientists to build an independent career in the investigation of the causes, diagnosis, treatment, prevention, or management of cancer or its side effects.

Matthew Rook awarded a Joan Wright Goodman Dissertation Fellowship

Monday, June 1, 2020

Matthew L. Rook, M.S. (MacLean Lab) has been awarded a Joan Wright Goodman Dissertation Fellowship for 2020-2021!  This fellowship was endowed by Joan Wright Goodman, PhD class of 1952, to support doctoral students across disciplines in the sciences.  It is one of the University’s most competitive dissertation fellowships and is given to students who display exceptional ability and promise.  It is a testimony to the University’s commitment to supporting your scholarship. 

The award is $20,000, and must be used over at least 9 months between July 1, 2020 and June 30, 2021. Congrats Matthew!

Meet Alexander Milliken: A School of Medicine and Dentistry Ambassador

Tuesday, February 4, 2020

Third year PhD student thrives on pushing boundaries

Alexander Milliken

Alexander Milliken

Alexander Milliken thrives on being challenged, pushing boundaries, and building community. He’s a third year graduate student at the School of Medicine and Dentistry (SMD), where he is pursuing a PhD in pharmacology.

Milliken is also part of SMD’s Ambassador Program, which connects current medical students, trainees, and PhD candidates with alumni through events, programs, tours, and other activities. Milliken and the other 27 SMD Ambassadors provide alumni a glimpse into the experience of current students and, in turn, alumni provide insights into their medical careers. “Being an ambassador gives me valuable volunteer experience,” Milliken says. “It helps me sharpen my leadership skills and make personal and professional contacts.” Milliken has met like-minded peers through the program, too—people he wouldn’t have met otherwise. And, he’s taken the concept of a multidisciplinary approach to a new level. For instance, he rock climbs with colleagues from immunology, microbiology, and virology. He works out at the River Campus fitness center with friends from neuroscience, pharmacology and toxicology. He plays in a softball league with biomedical engineering students, and he’s on a volleyball team with peers from biochemistry and biophysics.

When did you know you wanted a career in medicine? I always knew I wanted to pursue a career in medicine but after losing both my grandfather and one of my best friends to cardiac-related deaths, the decision was clear to start my career in research, pushing the boundaries of what we think we know.

Why cellular and molecular pharmacology? I was drawn to cellular and molecular pharmacology physiology because of the strong mitochondria research group. I can study the underlying molecular mechanisms of a pathology such as heart attack and then can begin to develop/screen novel therapeutics that could one day potentially make their way into the clinic. Mitochondria are the source of energy production in the cell and are starting to gain a significant amount of attention for their implications in many other diseases, pathologies, and syndromes.

Why did you want to go to the School of Medicine and Dentistry? I grew up in Rochester. I love it here and although I left the area for my undergraduate studies, SMD was my number one choice throughout the graduate school application process. The school is focused on answering rigorous scientific questions and sets the standard for how research should be done. The hospital, medical school, and graduate school are all under one roof, which allows for extensive collaboration among a vast array of research fields.

Why did you want to be an SMD Ambassador? Being an ambassador means that I am part of the group that helps connect generations of people associated with the University. We are all so lucky to be a part of the community here.

What do you enjoy most about being an Ambassador? A lot of the alumni I’ve met are MDs, not PhDs like me. What’s clear to me is that although our paths have been very different, there are a lot of similarities, including the rigorous training and the tremendous rewards of such hard work. We all share one thing in common: the University of Rochester experience. I particular enjoy how much the MDs are genuinely interested in PhD research when I have had the opportunity to talk with them at various networking events.

What’s a typical day like for you? Each day usually starts with responding to emails, checking for any new publications on PubMed, and finishing up calculations. Then, I will start an experiment, for instance, something related to surgery or mitochondria or cardiac cell isolation. After that, I analyze data from the experiment to see which direction the day has pushed me toward and where I need to focus my work tomorrow.

Suzanne Haber Honored by Society of Biological Psychiatry for Research on Mental Disorders

Thursday, January 30, 2020

Suzanne N. Haber, Ph.D., Dean’s Professor in the Department of Pharmacology and Physiology, will receive the Society of Biological Psychiatry’s 2020 Gold Medal Award at the Society’s 75th Annual Scientific Convention & Meeting in the spring. The award honors members of the Society whose significant and sustained work has advanced and extended knowledge on the neurobiology of mental illness.

Haber’s lab investigates the cortico-cortical and cortico-basal ganglia systems in the brain. Her work demonstrates the specific hard-wired connections that are associated with normal decision making, emotional and cognitive control, and the connectional abnormalities in those circuits that are linked to a wide range of mental health disorders, including obsessive-compulsive disorder (OCD), drug abuse and addiction, schizophrenia, and motor control disorders such as Parkinson’s disease.  This work has played a key role in targeting and interpreting the effects of noninvasive and invasive therapeutic approaches for OCD and depression.

For the past ten years, Haber has led the Silvio O. Conte Center for Basic and Translational Mental Health Research at the University of Rochester. Funded by the National Institute of Mental Health, the Center uses translational approaches to probe the neurocircuitry that underlies neuromodulation for OCD, pinpointing specific abnormalities within the brain circuits that are associated with the disease. This information is being used to guide new treatment options for the three million-plus Americans who live with the disorder.

“Suzanne’s seminal contributions to elucidating specific neural networks that control learning, decision-making, reward and motivation, and how pathologies associated with these neural communication hubs underlie multiple neurological, movement, and mental health disorders make her uniquely qualified to receive this prestigious career award,” said Robert T. Dirksen, Ph.D., Lewis Pratt Ross Professor and Chair of the Department of Pharmacology and Physiology. “Her work is making a difference in the lives of individuals and families suffering from neurological and mental health disorders. We are extremely proud that she represents the University of Rochester as a Society of Biological Psychiatry Gold Medal Award winner.”

The Society of Biological Psychiatry was founded in 1945 to emphasize the medical and scientific study and treatment of mental disorders. It’s the oldest neuropsychiatry research society in America, currently made up of more than 1,500 members from across the United States, Canada, Europe and Asia. Members conduct research in areas spanning from basic cellular studies to clinical trials and prevention research.

Haber, who is also a professor of Neuroscience, Brain and Cognitive Science, and Psychiatry, will split the 2020 Gold Medal Award with Carol Tamminga, M.D. of UT Southwestern Medical Center.

Jing Liu awarded a two-year American Heart Association predoctoral fellowship

Thursday, January 9, 2020

Jing Liu, graduate student in the laboratory of Dr. David A. Dean was awarded a two-year American Heart Association predoctoral fellowship entitled, “Role of MRCKa and Na+,K+-ATPase signaling in alveolar barrier function in the mouse lung”, beginning January 1, 2020.

Project Summary:
Acute Respiratory Distress Syndrome (ARDS) is a severe medical condition which is characterized by significant alveolar fluid accumulation and insufficient gas exchange. Cardiac surgery, ECMO, and use of cardiac medications are all known risk factors for ARDS which also complicates management of these and other cardiovascular diseases. Effective alveolar fluid clearance and repair of a functional alveolar-capillary barrier are considered the primary mechanisms for edema resolution in ARDS. Apart from enhancing fluid clearance, the Na+,K+-ATPase has been shown important for alveolar barrier function. Our lab showed that overexpression of the Na+,K+-ATPase b1 subunit into lungs enhances alveolar barrier integrity in previously injured lungs in mice and pigs. Previous in vitro data indicated that MRCKa mediates the upregulation of tight junction (TJ) proteins and epithelial barrier integrity by b1 overexpression. I hypothesize that the b1-Na+,K+-ATPase regulates alveolar barrier function through MRCKa in vivo. I will determine 1) whether MRCKa is required for the upregulation of TJ proteins and barrier function by b1 gene delivery in vivo, and 2) whether overexpression of MRCKa alone is sufficient to protect and/or treat lipopolysaccharides (LPS) induced lung injury in mice. LPS will be delivered by oropharyngeal aspiration to induce lung injury. Various plasmids will be delivered to mouse lungs by electroporation. For aim 1, plasmid to knockdown MRCKa or an MRCKa inhibitor will be delivered to lungs 24 hours before gene transfer of plasmid to overexpress b1. If required for signaling, MRCKa knockdown or inhibition will abolish b1's induction of TJ proteins and barrier upregulation. For aim 2, mice will be challenged with LPS 24 hours after (protection study) or before (treatment study) gene transfer. At end points, various assays will be performed to assess lung injury. It is expected that overexpression of MRCKa alone will be sufficient to protect and treat LPS induced acute lung injury, decreasing lung injury and increasing TJ expression; overexpression of both MRCKa and b1 subunit will augment the protection and treatment of LPS injured lungs to give the greatest reduction in lung injury and improvement in barrier function. These studies will increase our understanding of the pathogenesis and treatment of ARDS, improve lung health, and ultimately decrease cardiovascular complications.

Chongyang Zhang awarded a two-year American Heart Association predoctoral fellowship

Monday, January 6, 2020

Chongyang Zhang, graduate student in the laboratory of Dr. Chen Yan was awarded a two-year American Heart Association predoctoral fellowship entitled, “The role of PDE1C in vascular smooth muscle cell lysosomal dysfunction and atherosclerosis”, beginning January 1, 2020.

Project Summary:
The objective of this project is to investigate the function and underlying mechanism of the cyclic nucleotide phosphodiesterase 1C (PDE1C) in pathological vascular remodeling during atherogenesis. Cyclic AMP and cyclic GMP regulate vascular functions. PDEs by hydrolyzing cyclic nucleotides, regulate cyclic nucleotide signaling. Vascular smooth muscle cells (SMCs), upon endothelium damage, transit from contractile phenotype to synthetic phenotype. In vasculature, PDE1C expression is selectively induced in synthetic SMCs, but not in contractile SMCs or endothelial cells. Synthetic SMCs can accumulate oxidized low-density lipoprotein (oxLDL) in lysosomes, referred to as SMC-derived foam cells, that have been suggested to contribute significantly in atherosclerotic lesions. oxLDL accumulation in lysosome causes lysosome membrane permeabilization and lysosome dysfunction, which accelerates atherosclerosis progression. Our preliminary data demonstrate PDE1C deficiency significantly decreases atherosclerotic lesions in vivo. In synthetic SMCs in vitro, we found that PDE1C inhibition reduces lysosomal oxLDL accumulation and ameliorates lysosomal permeabilization. Therefore, we propose two specific aims. Aim1: Determine the roles and underlying mechanisms of PDE1C in the regulation of oxLDL accumulation and lysosomal permeabilization in synthetic SMCs in vitro. In SMCs culture, PDE1C deficiency will be examined by PDE1 activity inhibitor, PDE1C wildtype vs PDE1C knockout mouse SMCs, PDE1C shRNA, and PDE1C reconstitution by adenovirus. SMCs oxLDL accumulation and lysosomal permeabilization will be assessed by Acridine Orange staining, cathepsin B/D staining, and lysosomal galectin puncta assay. Underlying mechanistical studies will use pharmacological inhibitors, siRNA or shRNA. Aim2: Evaluate the effect of PDE1C deficiency on SMC lipid accumulation and lysosomal dysfunction in atherosclerotic lesions in vivo. We will use spontaneous atherosclerotic model induced by 4 months high fat diet in mouse for biochemical assessments in the lesion areas.

We will also examine the treatment potential of PDE1 inhibition on pre-trapped lipid deposition, using an accelerated atherosclerosis mouse model induced by carotid artery partial ligation. We hypothesize that PDE1C plays an essential role in atherosclerotic vascular modeling by promoting oxLDL induced-lysosomal dysfunction in synthetic SMC. This study may have significant therapeutic impact on atherosclerosis treatment.