Neurogenesis, neuronal migration, and axon guidance

Author(s):  
Andrea Accogli ◽  
Nassima Addour-Boudrahem ◽  
Myriam Srour
2018 ◽  
Vol 103 (6) ◽  
pp. 1009-1021 ◽  
Author(s):  
William B. Dobyns ◽  
Kimberly A. Aldinger ◽  
Gisele E. Ishak ◽  
Ghayda M. Mirzaa ◽  
Andrew E. Timms ◽  
...  

Cell ◽  
2006 ◽  
Vol 125 (1) ◽  
pp. 127-142 ◽  
Author(s):  
Guillermina López-Bendito ◽  
Aline Cautinat ◽  
Juan Antonio Sánchez ◽  
Franck Bielle ◽  
Nuria Flames ◽  
...  

2019 ◽  
Vol 11 ◽  
pp. 175883591985523 ◽  
Author(s):  
Zhengdong Jiang ◽  
Gang Liang ◽  
Ying Xiao ◽  
Tao Qin ◽  
Xin Chen ◽  
...  

The SLITs (SLIT1, SLIT2, and SLIT3) are a family of secreted proteins that mediate positional interactions between cells and their environment during development by signaling through ROBO receptors (ROBO1, ROBO2, ROBO3, and ROBO4). The SLIT/ROBO signaling pathway has been shown to participate in axonal repulsion, axon guidance, and neuronal migration in the nervous system and the formation of the vascular system. However, the role of the SLIT/ROBO pathway has not been thoroughly clarified in tumor development. The SLIT/ROBO pathway can produce both beneficial and detrimental effects in the growth of malignant cells. It has been confirmed that SLIT/ROBO play contradictory roles in tumorigenesis. Here, we discuss the tumor promotion and tumor suppression roles of the SLIT/ROBO pathway in tumor growth, angiogenesis, migration, and the tumor microenvironment. Understanding these roles will help us develop more effective cancer therapies.


2018 ◽  
Author(s):  
Inés González-Calvo ◽  
Fekrije Selimi

AbstractMany proteins initially identified in the immune system play roles in neurogenesis, neuronal migration, axon guidance, synaptic plasticity and other processes related to the formation and refinement of neural circuits. Although the function of the immune-related protein Galectin-3 (LGALS3) has been extensively studied in the regulation of inflammation, cancer and microglia activation, little is known about its role in the development of the brain. In this study, we identified that LGALS3 is expressed in the developing postnatal cerebellum. More precisely, LGALS3 is expressed by cells in meninges and in the choroid plexus, and in subpopulations of astrocytes and of microglial cells in the cerebellar cortex. Analysis of Lgals3 knockout mice showed that Lgals3 is dispensable for the development of cerebellar cytoarchitecture and Purkinje cell excitatory synaptogenesis in the mouse.


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