Purkinje Cell Migration and Differentiation

2021 ◽  
pp. 173-205
Author(s):  
Constantino Sotelo ◽  
Ferdinando Rossi
Keyword(s):  
Cell Reports ◽  
2017 ◽  
Vol 18 (2) ◽  
pp. 367-379 ◽  
Author(s):  
Maria Christina Sergaki ◽  
Carlos F. Ibáñez
Keyword(s):  

2020 ◽  
Author(s):  
Hassan Marzban ◽  
Maryam Rahimi-Balaei ◽  
Xiaodan Jiao ◽  
Azadeh Dalvand ◽  
Shahin Shabanipour ◽  
...  

Abstract Introduction: Microglia are the immune cells of the central nervous system that are involved in a variety of developmental processes such as regulation of cell death and survival, spatial patterning, and contribute to the development of Purkinje cells during migration. Microglia express immunoglobulin G Fc receptors (FcgRs). Hypothesis: In this report, we describe microglial FcgR expression in the cerebellum during development related to abnormal Purkinje cell migration. Method: To detect microglial FcgR, the direct anti-IgG (secondary antisera) and high concentrations of Triton X-100 were applied as a method for labeling microglial cells without the use of any specific primary antiserum. By using the Acp2 -/- mice, which show an excessive Purkinje cell migration into the molecular layer combined with the different knockout mice altering the Reelin pathway (Reeler, Scrambler, and Apoer2 -/- mice), that Purkinje cells are ectopically located in white matter. Result: We show the expression of microglial FcgRs in the cerebellum of these mice is absent, but not in the Acp2 -/- mice . Discussion: These results suggest a role for FcgRs in reelin signaling pathway, not related to Purkinje cell migration, but may be an adaptation to the environment with the large number of ectopic Purkinje cells. Conclusion: However, the exact correlation between the ectopic Purkinje cells presence and FcgRs absence in reeler, Scrambler, Apoer -/- mice and the presence of FcgRs in Acp2 -/- mutant are yet to be determined.


Author(s):  
J. Roemer ◽  
S.R. Simon

We are developing an in vitro interstitial extracellular matrix (ECM) system for study of inflammatory cell migration. Falcon brand Cyclopore membrane inserts of various pore sizes are used as a support substrate for production of ECM by R22 rat aortic smooth muscle cells. Under specific culture conditions these cells produce a highly insoluble matrix consisting of typical interstitial ECM components, i.e.: types I and III collagen, elastin, proteoglycans and fibronectin.


2019 ◽  
Vol 63 (5) ◽  
pp. 579-594 ◽  
Author(s):  
Guillem Lambies ◽  
Antonio García de Herreros ◽  
Víctor M. Díaz

Abstract Cell migration is a multifactorial/multistep process that requires the concerted action of growth and transcriptional factors, motor proteins, extracellular matrix remodeling and proteases. In this review, we focus on the role of transcription factors modulating Epithelial-to-Mesenchymal Transition (EMT-TFs), a fundamental process supporting both physiological and pathological cell migration. These EMT-TFs (Snail1/2, Twist1/2 and Zeb1/2) are labile proteins which should be stabilized to initiate EMT and provide full migratory and invasive properties. We present here a family of enzymes, the deubiquitinases (DUBs) which have a crucial role in counteracting polyubiquitination and proteasomal degradation of EMT-TFs after their induction by TGFβ, inflammatory cytokines and hypoxia. We also describe the DUBs promoting the stabilization of Smads, TGFβ receptors and other key proteins involved in transduction pathways controlling EMT.


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