TY - JOUR
T1 - Ataxia-Telangiectasia mutated plays an important role in cerebellar integrity and functionality
AU - Mitiagin, Yulia
AU - Barzilai, Ari
N1 - Publisher Copyright:
© 2023 Wolters Kluwer Medknow Publications. All rights reserved.
PY - 2023/3
Y1 - 2023/3
N2 - Accumulating evidence indicates that ataxia-Telangiectasia mutated kinase is critical for maintaining cellular homeostasis and that it has both nuclear and cytoplasmic functions. However, the functions of ataxia-Telangiectasia mutated that when lost lead to cerebellar degeneration are still unknown. In this review, we first describe the role of ataxia-Telangiectasia mutated in cerebellar pathology. In addition to its canonical nuclear functions in DNA damage response circuits, ataxia-Telangiectasia mutated functions in various cytoplasmic and mitochondrial processes that are critically important for cellular homeostasis. We discuss these functions with a focus on the role of ataxia-Telangiectasia mutated in maintaining the homeostatic redox state. Finally, we describe the unique functions of ataxia-Telangiectasia mutated in various types of neuronal and glial cells including cerebellar granule neurons, astrocytes, and microglial cells.
AB - Accumulating evidence indicates that ataxia-Telangiectasia mutated kinase is critical for maintaining cellular homeostasis and that it has both nuclear and cytoplasmic functions. However, the functions of ataxia-Telangiectasia mutated that when lost lead to cerebellar degeneration are still unknown. In this review, we first describe the role of ataxia-Telangiectasia mutated in cerebellar pathology. In addition to its canonical nuclear functions in DNA damage response circuits, ataxia-Telangiectasia mutated functions in various cytoplasmic and mitochondrial processes that are critically important for cellular homeostasis. We discuss these functions with a focus on the role of ataxia-Telangiectasia mutated in maintaining the homeostatic redox state. Finally, we describe the unique functions of ataxia-Telangiectasia mutated in various types of neuronal and glial cells including cerebellar granule neurons, astrocytes, and microglial cells.
KW - ATM
KW - DNA damage response
KW - ataxia telangiectasia
KW - cerebellum
KW - double-strand breaks
KW - mitochondrial dysfunction
KW - oxidative stress
KW - single-strand breaks
UR - http://www.scopus.com/inward/record.url?scp=85137344704&partnerID=8YFLogxK
U2 - 10.4103/1673-5374.350194
DO - 10.4103/1673-5374.350194
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C2 - 36018153
AN - SCOPUS:85137344704
SN - 1673-5374
VL - 18
SP - 497
EP - 502
JO - Neural Regeneration Research
JF - Neural Regeneration Research
IS - 3
ER -