Behavioral Effect of IgSF9b in the Prefrontal Cortex Abstract IgSF9b was recently identified as a high-risk gene strongly associated with negative symptoms of schizophrenia (SZ) and major depressive disorders (MDD). IgSF9b gene codes for adhesion protein IgSF9b, which is specifically expressed in the brain, especially in the forebrain region of the neocortex. In vitro studies indicate IgSF9b is primarily expressed in GABAergic interneurons and subset of pyramidal neurons, with coupling to neuroligin 2 to promote inhibitory signaling. However, whether and how IgSF9b deficiency affects cognitive and social behaviors, especially those related to social withdrawal and anhedonia, remains untested. We endeavored to explore the functional roles of protein IgSF9b in the medial prefrontal cortex (mPFC) in the regulation of motivational and social behaviors as this brain region is highly associated with executive function, cognition, and social behavior control, as well as deficits related to depression and SZ. Our studies aim to elucidate the fundamental physiological role of protein IgSF9b, at a cellular, circuit, and behavioral level. In our pilot study, we performed successful knockdown (KD) of protein IgSF9b in the young adult mouse mPFC, and interestingly, we found that IgSF9b KD significantly impairs both social preference and social memory. We hypothesize that selective KD of IgSF9b impairs behaviors associated with social withdrawal and anhedonia by reducing inhibition and affecting neurons projecting to subcortical areas related to social behavior such as nucleus accumbens (NAc). We will first evaluate the effects of IgSF9b KD in the mPFC on motivational and social withdrawal behaviors and then determine whether IgSF9b KD in the mPFC selectively affects the mPFC-NAc pathway to regulate social behaviors. IgSF9b is mainly expressed in the forebrain of the neocortex and is proposed to be highly associated with negative symptoms. Therefore, examining the effects of IgSF9b on mPFC-associated behaviors has the potential to elucidate unidentified mechanisms of behavioral deficits seen in neuropsychiatric diseases such as SZ.

Public Health Relevance

IgSF9b has recently been identified as one of the high-risk genes for negative symptoms of schizophrenia. However, the basic physiological function of IgSF9b in the regulation of behavior remains unexplored. This study aims to explore if knockdown of IgSF9b level in the medial prefrontal cortex can produce circuit-specific behavioral changes. Our findings will provide novel insights into the physiological function of protein IgSF9b associated with prefrontal function.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Exploratory/Developmental Grants (R21)
Project #
1R21MH121836-01A1
Application #
10054717
Study Section
Molecular Neuropharmacology and Signaling Study Section (MNPS)
Program Officer
Winsky, Lois M
Project Start
2020-08-01
Project End
2022-07-30
Budget Start
2020-08-01
Budget End
2022-07-30
Support Year
1
Fiscal Year
2020
Total Cost
Indirect Cost
Name
Drexel University
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
002604817
City
Philadelphia
State
PA
Country
United States
Zip Code
19102