scholarly journals Reciprocal repulsions instruct the precise assembly of parallel hippocampal networks

Science ◽  
2021 ◽  
Vol 372 (6546) ◽  
pp. 1068-1073
Author(s):  
Daniel T. Pederick ◽  
Jan H. Lui ◽  
Ellen C. Gingrich ◽  
Chuanyun Xu ◽  
Mark J. Wagner ◽  
...  

Mammalian medial and lateral hippocampal networks preferentially process spatial- and object-related information, respectively. However, the mechanisms underlying the assembly of such parallel networks during development remain largely unknown. Our study shows that, in mice, complementary expression of cell surface molecules teneurin-3 (Ten3) and latrophilin-2 (Lphn2) in the medial and lateral hippocampal networks, respectively, guides the precise assembly of CA1-to-subiculum connections in both networks. In the medial network, Ten3-expressing (Ten3+) CA1 axons are repelled by target-derived Lphn2, revealing that Lphn2- and Ten3-mediated heterophilic repulsion and Ten3-mediated homophilic attraction cooperate to control precise target selection of CA1 axons. In the lateral network, Lphn2-expressing (Lphn2+) CA1 axons are confined to Lphn2+ targets via repulsion from Ten3+ targets. Our findings demonstrate that assembly of parallel hippocampal networks follows a “Ten3→Ten3, Lphn2→Lphn2” rule instructed by reciprocal repulsions.

1999 ◽  
Vol 190 (1) ◽  
pp. 65-74 ◽  
Author(s):  
Hidehiro Kishimoto ◽  
Jonathan Sprent

Repeated attempts to show that costimulation for negative selection is controlled by a single cell surface molecule have been unsuccessful. Thus, negative selection may involve multiple cell surface molecules acting in consort. In support of this idea, we show here that at least three cell surface molecules, namely CD28, CD5, and CD43, contribute to Fas-independent negative selection of the tolerance-susceptible population of heat-stable antigen (HSA)hiCD4+8− cells found in the medulla. The costimulatory function of these three molecules can be blocked by certain cytokines, IL-4 and IL-7, and coinjecting these cytokines with antigen in vivo abolishes negative selection; Fas-dependent negative selection, however, is maintained. The results suggest that efficient negative selection requires the combined functions of at least four cell surface molecules: CD28, CD5, CD43, and Fas.


Neuron ◽  
2008 ◽  
Vol 59 (6) ◽  
pp. 972-985 ◽  
Author(s):  
Mitsuhiko Kurusu ◽  
Amy Cording ◽  
Misako Taniguchi ◽  
Kaushiki Menon ◽  
Emiko Suzuki ◽  
...  

1991 ◽  
Vol 266 (15) ◽  
pp. 9697-9702 ◽  
Author(s):  
A.H. Limper ◽  
B.J. Quade ◽  
R.M. LaChance ◽  
T.M. Birkenmeier ◽  
T.S. Rangwala ◽  
...  

Neuroscience ◽  
1996 ◽  
Vol 73 (1) ◽  
pp. 161-169 ◽  
Author(s):  
G. Gopinath ◽  
V. Sable ◽  
K. Sailaja ◽  
P.N. Tandon

2011 ◽  
Vol 134 (2) ◽  
pp. 113-121 ◽  
Author(s):  
Laia Llinàs ◽  
Adriana Lázaro ◽  
Jose de Salort ◽  
Jessica Matesanz-Isabel ◽  
Jordi Sintes ◽  
...  

Author(s):  
D. N. J. Hart ◽  
G. J. Clark ◽  
J. W. Dekker ◽  
D. B. Fearnley ◽  
M. Kato ◽  
...  

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