Any man could,

if he were so inclined,

be the sculptor of his own brain.

-Santiago Ramón y Cajal

 
 

Overview of Research in the Kopec Lab

When asked to think of brain development, one often pictures babies developing in utero, learning to speak, or triumphantly climbing the stairs of the school bus in their "first day of school" outfit. These are all momentous developmental steps in brain and psychological development. But brain development actually continues well past these stages, even into young adulthood. Decreases in grey matter density is a normal developmental process that continues in some brain regions well into ones twenties (right; image from Gogtay et al. 2004). 

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Brain regions associated with decision making and reward processing develop during adolescence. these regions are particularly vulnerable during this time and can be altered by stressors common to the human adolescent experience, such as drug use or social stress.

 

Microglia, the brain's immune cells, regulate both brain development and its response to experience. In development, microglia eliminate connections between neurons, known as synaptic pruning, which we think is related to decreases in grey matter (above). And, as immune cells, microglia's primary role is surveillance (left; acquired by Dr. Richa Hanamsagar). This allows microglia to rapidly respond to change, including changes in psychological state, like emotions, or bodily state, like the presence of addictive substances.

Dr. Kopec's previous work demonstrated that during adolescent development, microglia eliminate (or prune) dopamine receptors in reward regions in male, but not female rats. This immune process was responsible for normal developmental changes in social behavior over the course of adolescence.

By extension, any stimulus or experience that can activate dopamine or immune signaling has the potential to interact with adolescent brain development and re-route it in ways that will lastingly change brain wiring and behavior.

 

Moreover, because dopaminergic brain development in adolescence is regulated in sex-specific ways, experience is likely to be interpreted by the brain in a sex-specific manner and result in sex-specific outcomes. Interestingly, a variety of neuropsychiatric disorders associated with dopaminergic and/or immune signaling that 'emerge' during, or are strongly influenced by, the adolescent developmental period have sex-biased presentations, for instance ADHD in males and depression in females (right; image from McCarthy 2016). 

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What stimuli or experiences affect dopamine and/or immune signaling?

Answer: All of the things.

The Kopec lab seeks to understand how the adolescent brain develops in sex-specific ways, and how adolescent experience interacts with this development to lastingly alter brain circuits and behavior. We are particularly interested in how microglia and immune signaling might be at the crossroads between development and experience, serving to re-route neural development and communication down one path or another. 

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After all, if the brain develops in sex specific-ways, responds to experience in sex-specific ways, and neurological disorders emerge in sex-specific ways, then we will likely require sex-specific pharmacological and behavioral treatments to combat pathological states (left; from AAPS).

#haveyousciencedyettoday

The Kopec Lab Mission

Research

The Kopec lab aims to use basic science studying the intersection between experience and adolescent brain development, in particular neuro-immune development, to advance our understanding and treatment of sex-specific neurological disorders. 

We will achieve this by producing high quality research that is reproducible, creative, and thorough. This requires:

1) valuing literature reviews and discussing new research in journal clubs, 

2) planning, planning again, and then planning a third time before performing experiments,

3) optimizing experiments to attain the most interpretable data possible,

4) leveraging our environment at Albany Medical Center by engaging with clinical expertise to ensure the questions we are asking and models we are developing are translationally relevant, and

5) a sincere and unwavering commitment to training and developing exceptional scientists.

Mentorship

We all screw up. It's inevitable. Failure is part and parcel of academia. What really matters, is what happens next.

The Kopec lab values mentorship and supported development in both the personal and professional arenas. Each lab member will have the opportunity to regularly evaluate his/her scholarly and career goals, and how to negotiate those needs with personal needs. Dr. Kopec will be the first to admit she hasn't always done this right, but the culture she wants to instill is one in which (1) you screw up (again, as we all do), (2) we, as a team, work together to figure out what happened and how to move forward, (3) then you do so.

On a related note, academia will not be the last stop for everyone's career. The Kopec lab fully supports other ways of using your numerous skills, and Dr. Kopec is dedicated to helping you find what brings the absolute best out of your talents and makes you happy.

Communication

The Kopec lab believes communication is key for scientists. To develop communication skills, ample opportunities will be provided to practice writing and speaking aimed at different audiences. A talk given to a room full of scientists will look a lot different from a talk given to a room full of community members. A grant application will look a lot different from a manuscript submitted for publication. A well-rounded communication toolkit is essential and the Kopec lab will help you build it.

Furthermore, interpersonal communication is key for team success and workplace satisfaction. Dr. Kopec will prioritize open communication and constructive discussions, and she expects other lab colleagues to do so as well. 

Outreach and education

The Kopec lab is excited to integrate into and contribute to the Albany community! All outreach and educational endeavors will be fully encouraged, and ideally a team effort. We look forward to expanding this section as our lab grows in Albany. Previous examples of Dr. Kopec's outreach effort include volunteering for the BioBus, mentoring through the New York Academy of Sciences, and hosting the Science Olympiad winners for a lecture during 2017-2018's Society for Neuroscience meetings.

 

Principal Investigator

Dr. Ashley M. Kopec

I grew up in Wisconsin and received my Bachelor's degree in Psychology from the liberal arts institution, Carroll University. My interest in research began with a summer research program sponsored by Amgen at UC San Francisco, and eventually motivated me to earn my PhD from NYU's Center for Neural Science under the mentorship of Dr. Thomas Carew. My NRSA F31-supported thesis focused on the role of different growth factors simultaneously engaged during long-term memory formation.  I completed my postdoctoral work with Dr. Staci Bilbo at Duke University and Harvard Medical School/Mass General Hospital, where my NRSA F32-supported project focused on the neuro-immune mechanisms of adolescent brain and behavioral development. I am now continuing my academic journey as an Assistant Professor in the Department of Neuroscience and Experimental Therapeutics at Albany Medical College, starting in Nov. 2018. In addition to research, I love teaching, reading, watching sports, and spending time with my husband, Dan, and two fur babies, Milo and Brave Champion (yes, you read that right). Go Pack Go!

Lab Manager/Technician

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Christopher Figueroa, B.S.

I received my undergraduate education from Franciscan University of Steubenville.  During my undergraduate studies, I spent a summer as an intern for AVM Biotechnology in Seattle, WA, which was my first experience in biomedical research.  After that experience, I knew that I wanted to pursue research as a career after college; I was hooked.  I went on to graduate in the winter of 2017 with a B.S. in Biology.  Up to this point, I had not had any contact with neuroscience and barely any research experience to my name. However, I was accepted into the Postbaccalaureate IRTA program at the NIH and went on to spend a year working on autism research under Dr. Beebe Smith.  My first experience with neuroscience was a positive one, so I decided to continue pursuing a career in neuroscience research, which led me to this very website!  After reading about Dr. Kopec’s ideas for her research, I immediately applied for the Research Technician position and excitedly accepted her offer to join the lab.  Outside of research, I especially enjoy spending time with my wife, playing music and board/card games, Marvel and DC comics and pretty much anything outdoors.

Postdoctoral Fellows

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Justin bourgeois, phd (anticipated april 2019)

Justin will be joining the Kopec lab in April 2019 - stay tuned for his bio!

Graduate Students

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David ndambuki, b.s. (anticipated may 2019)

David is joining the PhD program in Neuroscience, and will be rotating with the Kopec lab. Stay tuned for his bio!


 

Undergraduate Students

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Helen Yang

Helen is an undergraduate from Northeastern joining the Kopec lab for summer 2019. Stay tuned for her bio!

 

The Kopec lab is always open to new innovative and enthusiastic colleagues! If you are interested in joining the lab, please contact Dr. Kopec with a cover letter and CV at kopeclab@gmail.com

Publications

Dr. Kopec's complete works on Pubmed can be found here. Below you will find individual publications with a linked PDF. For information regarding on-going projects, please feel free to contact us!

Kopec AM, Smith CJ, Bilbo SD. (2019). Neuro-immune mechanisms regulating social behavior: Dopamine as mediator? Trends in Neuroscience, S0166-2236(19): 30022-0.

Kopec AM, Smith CJ, Ayre NR, Sweat SC, Bilbo SD. (2018). Microglial dopamine receptor elimination defines sex-specific nucleus accumbens development and social behavior in adolescent rats. Nature Communications, 9(1): 3769.

*This study received media attention (here), was selected by Nat Comms editors for a press release (here) and feature (here), was recommended twice by F1000 (below), and got a shoutout from the director of the NIH (here)!*

Access the recommendation on F1000Prime

Kopec AM, Fiorentino MR, Bilbo SD. (2018). Gut-immune-brain dysfunction in Autism: Importance of sex. Brain Research, S0006-8993(18): 30017-19.

Lacagnina MJ, Kopec AM, Cox SS, Hanamsagar R, Wells C, Slade S, Grace PM, Watkins LR, Levin ED, Bilbo SD. (2017). Opioid Self-Administration is Attenuated by Early-Life Experience and Gene Therapy for Anti-Inflammatory IL-10 in the Nucleus Accumbens of Male Rats. Neuropsychopharmacology, 42(11): 2128-40.

Kopec AM, Rivera PD, Lacagnina MJ, Hanamsagar R, Bilbo SD. (2017). Optimized solubilization of TRIzol-precipitated protein permits Western blotting analysis to maximize data available from brain tissue. Journal of Neuroscience Methods, 280: 64-76.

Mirisis AA*, Alexandrescu A*, Carew TJ, Kopec AM. (2016). The contribution of spatial and temporal networks in the induction of long-term memory and its underlying synaptic plasticity. Aims Neuroscience, 3(3): 356-84. 

Stough S*, Kopec AM*, Carew TJ. (2015). Synaptic generation of an intracellular retrograde signal requires activation of the tyrosine kinase and mitogen-activated protein kinase signaling cascades in Aplysia. Neurobiology of Learning and Memory, 125: 47-54. *indicates co-first authorship

Kopec AM, Philips GT, Carew TJ. (2015). Distinct growth factor families are recruited in unique spatiotemporal domains during long-term memory formation in Aplysia californica. Neuron, 86(5): 1228-39. 

Fischbach S*, Kopec AM*, Carew TJ (2014). Activity-dependent inhibitory gating in molecular signaling cascades induces a novel form of intermediate-term synaptic facilitation in Aplysia californica. Learning and Memory, 21(4): 199-204. *indicates co-first authorship

 Pu L, Kopec AM, Boyle HD, Carew TJ (2014). A novel cysteine-rich neurotrophic factor in Aplysia facilitates neuronal growth, MAPK activation, and long-term synaptic facilitation in identified sensory neurons. Learning and Memory, 21(4): 215-222.

Kopec AM & Carew TJ (2013). Growth factor signaling and memory formation: Temporal and spatial integration of a molecular network. Learning & Memory, 20(10): 531-539.

Philips GT, Kopec AM, Carew TJ (2013). Pattern and predictability in memory formation: From molecular mechanisms to clinical relevance. Neurobiology of Learning and Memory, 105: 117-124.

Philips GT, Ye X, Kopec AM, Carew TJ (2013). MAPK establishes a molecular context that defines effective training patterns for long-term memory formation. The Journal of Neuroscience, 33(17): 7565-73.

Contact the Kopec lab

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The Kopec lab doors opened in Nov. 2018 at Albany Medical College in New York. Albany is a fun, affordable city with lots to do and see! From hiking and kayaking to dining and dancing, there is something for everyone in Albany. As the geographical oddity it is, Albany is also only a few hours from New York City, Boston, and Montreal for when you get a craving for big-city flavors. 

The Kopec lab would love to hear from you! Whether you'd like to join the lab, chat about science, or offer a general comment or question, we welcome your input. You can reach us at kopeclab@gmail.com, or just message us from here! To stay up-to-date, follow Dr. Kopec on Twitter.

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