Difference between revisions of "ICLM Journal Club"

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(This Friday - January 20, 2023 (9:30 am, in person, Gonda 1357))
(No ICLM this Friday - January 27, 2023. See you next week!)
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=<font color="blue">'''No ICLM this Friday - January 27, 2023. See you next week!'''</font>=
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=<font color="blue">'''This Friday - February 3, 2023 (9:30 a.m., in person, Gonda 1357)'''</font>=
  
<u>Speaker:</u> '' ''
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<u>Speaker:</u> ''Jamie Mondello''
  
<u>Title:</u> ''' '''
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<u>Title:</u> '''Topographic representation of current and future threats in the mouse nociceptive amygdala'''
  
<u>Summary:</u>  
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<u>Summary:</u> Adaptive behaviors arise from an integration of current sensory context and internal representations of past experiences. The central amygdala (CeA) is positioned as a key integrator of cognitive and affective signals, yet it remains unknown whether individual populations simultaneously carry current- and future-state representations. We find that a primary nociceptive population within the CeA of mice, defined by CGRP-receptor (Calcrl) expression, receives topographic sensory information, with spatially defined representations of internal and external stimuli. While Calcrl+ neurons in both the rostral and caudal CeA respond to noxious stimuli, rostral neurons promote locomotor responses to externally sourced threats, while caudal CeA Calcrl+ neurons are activated by internal threats and promote passive coping behaviors and associative valence coding. During associative fear learning, rostral CeA Calcrl+ neurons stably encode noxious stimulus occurrence, while caudal CeA Calcrl+ neurons acquire predictive responses. This arrangement supports valence-aligned representations of current and future threats for the generation of adaptive behaviors.
  
 
<u>Relevant Papers:</u>
 
<u>Relevant Papers:</u>
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[https://www.nature.com/articles/s41467-023-35826-4 Topographic representation of current and future threats in the mouse nociceptive amygdala, ''Bowen, A. J., Huang, Y. W., Chen, J. Y., Pauli, J. L., Campos, C. A., & Palmiter, R. D.,'' Nat Comm (2023)]
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[https://www.sciencedirect.com/science/article/pii/S0092867415007758?via%3Dihub Elucidating an affective pain circuit that creates a threat memory, ''Han, S., Soleiman, M. T., Soden, M. E., Zweifel, L. S., & Palmiter, R. D.,'' Cell (2015)]
  
 
='''About Us'''=
 
='''About Us'''=

Revision as of 02:01, 1 February 2023

This Friday - February 3, 2023 (9:30 a.m., in person, Gonda 1357)

Speaker: Jamie Mondello

Title: Topographic representation of current and future threats in the mouse nociceptive amygdala

Summary: Adaptive behaviors arise from an integration of current sensory context and internal representations of past experiences. The central amygdala (CeA) is positioned as a key integrator of cognitive and affective signals, yet it remains unknown whether individual populations simultaneously carry current- and future-state representations. We find that a primary nociceptive population within the CeA of mice, defined by CGRP-receptor (Calcrl) expression, receives topographic sensory information, with spatially defined representations of internal and external stimuli. While Calcrl+ neurons in both the rostral and caudal CeA respond to noxious stimuli, rostral neurons promote locomotor responses to externally sourced threats, while caudal CeA Calcrl+ neurons are activated by internal threats and promote passive coping behaviors and associative valence coding. During associative fear learning, rostral CeA Calcrl+ neurons stably encode noxious stimulus occurrence, while caudal CeA Calcrl+ neurons acquire predictive responses. This arrangement supports valence-aligned representations of current and future threats for the generation of adaptive behaviors.

Relevant Papers:

Topographic representation of current and future threats in the mouse nociceptive amygdala, Bowen, A. J., Huang, Y. W., Chen, J. Y., Pauli, J. L., Campos, C. A., & Palmiter, R. D., Nat Comm (2023)

Elucidating an affective pain circuit that creates a threat memory, Han, S., Soleiman, M. T., Soden, M. E., Zweifel, L. S., & Palmiter, R. D., Cell (2015)

About Us

Introduction

The Integrative Center for Learning and Memory (ICLM) is a multidisciplinary center of UCLA labs devoted to understanding the neural basis of learning and memory and its disorders. This will require a unified approach across different levels of analysis, including;

1. Elucidating the molecular cellular and systems mechanisms that allow neurons and synapses to undergo the long-term changes that ultimately correspond to 'neural memories'.

2. Understanding how functional dynamics and computations emerge from complex circuits of neurons, and how plasticity governs these processes.

3. Describing the neural systems in which different forms of learning and memory take place, and how these systems interact to ultimately generate behavior and cognition.

History of ICLM

The Integrative Center for Learning and Memory formally LMP started in its current form in 1998, and has served as a platform for many interactions and collaborations within UCLA. A key event organized by the group is the weekly ICLM Journal Club. For more than 10 years, graduate students, postdocs, principal investigators, and invited speakers have presented on topics ranging from the molecular mechanisms of synaptic plasticity, through computational models of learning, to behavior and cognition. Dean Buonomano oversees the ICLM journal club with help of student/post doctoral organizers. For other events organized by ICLM go to http://www.iclm.ucla.edu/Events.html.

Current Organizers:

Saray Soldado (Buonomano Lab) & Lukas Oesch (Churchland Lab). Please email us at iclm.journalclub@gmail.com if you would like to get regular updates regarding our journal club and weekly reminders.

Current Faculty Advisor:

Dean Buonomano


Past Organizers:

i) Anna Matynia(Aug 2004 - Jun 2008) (Silva Lab)

ii) Robert Brown (Aug 2008 - Jun 2009) (Balleine Lab)

iii) Balaji Jayaprakash (Aug 2008 - Nov 2011) (Silva Lab)

iv) Justin Shobe & Thomas Rogerson (Dec 2011 - June 2013) (Silva Lab)

v) Walt Babiec (O'Dell Lab) (2013-2014)

vi) Walt Babiec (O'Dell Lab) & Helen Motanis (Buonomano Lab) (2014-2017)

vii) Helen Motanis (Buonomano Lab) & Shonali Dhingra (Mehta Lab) (2017-2018)

viii) Shonali Dhingra (Mehta Lab) (2018-2020)

ix) Megha Sehgal (Silva Lab) & Giselle Fernandes (Silva Lab) (2020-2022)

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