scholarly journals Three decades of Cdk5

2021 ◽  
Vol 28 (1) ◽  
Author(s):  
Ping-Chieh Pao ◽  
Li-Huei Tsai

AbstractCdk5 is a proline-directed serine/threonine protein kinase that governs a variety of cellular processes in neurons, the dysregulation of which compromises normal brain function. The mechanisms underlying the modulation of Cdk5, its modes of action, and its effects on the nervous system have been a great focus in the field for nearly three decades. In this review, we provide an overview of the discovery and regulation of Cdk5, highlighting recent findings revealing its role in neuronal/synaptic functions, circadian clocks, DNA damage, cell cycle reentry, mitochondrial dysfunction, as well as its non-neuronal functions under physiological and pathological conditions. Moreover, we discuss evidence underscoring aberrant Cdk5 activity as a common theme observed in many neurodegenerative diseases.

Cancers ◽  
2019 ◽  
Vol 11 (2) ◽  
pp. 145 ◽  
Author(s):  
Ahmed Maklad ◽  
Anjana Sharma ◽  
Iman Azimi

Calcium signaling, in addition to its numerous physiological roles, is also implicated in several pathological conditions including cancer. An increasing body of evidence suggest critical roles of calcium signaling in the promotion of different aspects of cancer, including cell proliferation, therapy resistance and metastatic-related processes. In many cases, this is associated with altered expression and/or activity of some calcium channels and pumps. Brain cancers have also been the subject of many of these studies. In addition to diverse roles of calcium signals in normal brain function, a number of proteins involved in calcium transport are implicated to have specific roles in some brain cancers including gliomas, medulloblastoma, neuroblastoma and meningioma. This review discusses research that has been conducted so far to understand diverse roles of Ca2+-transporting proteins in the progression of brain cancers, as well as any attempts to target these proteins towards a therapeutic approach for the control of brain cancers. Finally, some knowledge gaps in the field that may need to be further considered are also discussed.


2012 ◽  
Vol 33 (4) ◽  
pp. e65-e65
Author(s):  
M. del Mar Carmona Abellán ◽  
M. Murie Fernández ◽  
P. Esteve Belloch

2015 ◽  
Vol 86 (11) ◽  
pp. e4.155-e4
Author(s):  
Ray Wynford-Thomas ◽  
Rob Powell

Just as ‘no man is an island’, despite its misleading name, the insula is not an island. Sitting deeply within the cerebrum, the insular cortex and its connections play an important role in both normal brain function and seizure generation. Stimulating specific areas of the insula can produce somatosensory, viscerosensory, somatomotor and visceroautonomic symptoms, as well as effects on speech processing and pain. Insular onset seizures are rare, but may mimic both temporal and extra-temporal epilepsy and if not recognised, may lead to failure of epilepsy surgery. We therefore highlight the semiology of insular epilepsy by discussing three cases with different auras. Insular onset seizures can broadly be divided into three main types both anatomically and according to seizure semiology:1. Seizures originating in the antero-inferior insula present with laryngeal constriction, along with visceral and gustatory auras (similar to those originating in medial temporal structures).2. Antero-superior onset seizures can have a silent onset, but tend to propagate rapidly to motor areas causing focal motor or hypermotor seizures.3. Seizures originating in the posterior insula present with contralateral sensory symptoms.


2019 ◽  
Vol 8 (3) ◽  
pp. 613-618

Neurochemical transmitters in the brain are fundamental to normal brain function and this investigation aims to introduce a study on the center of neuroscientific through an account of language development which conducts human speech mechanism using theoretical methods. In the process of this work, new understanding has been gained from the neurochemistry of several important neurotransmitters of dopamine (DA), epinephrine (EN), norepinephrine (NE), histamine (HA) and serotonin (ST) in brain by Monte Carlo simulation (MC) which uses the increased temperature to the potential energy of the neurochemicals in the brain considering the geometry optimization of the compounds as an additional conformational level. Moreover, the results of optimized DA, EN, NE, HA, ST neurochemical transmitters by running the physicochemical parameters as a practical model using Gaussian 09 program package can approve the twisting of language-brain due to these structures using density electron deliverers. The most stable of these compounds through the active sites of nitrogen and oxygen atoms has illustrated the best optimized position for localizing the structure through delivery technique in the brain to activate the center of learning a language as a simulated model. So, the best results with the calculated amounts conduct us to analyze the perspective of language learning process and enhancing this ability.


eLife ◽  
2016 ◽  
Vol 5 ◽  
Author(s):  
Gilad D Evrony ◽  
Eunjung Lee ◽  
Peter J Park ◽  
Christopher A Walsh

Whether somatic mutations contribute functional diversity to brain cells is a long-standing question. Single-neuron genomics enables direct measurement of somatic mutation rates in human brain and promises to answer this question. A recent study (<xref ref-type="bibr" rid="bib65">Upton et al., 2015</xref>) reported high rates of somatic LINE-1 element (L1) retrotransposition in the hippocampus and cerebral cortex that would have major implications for normal brain function, and suggested that these events preferentially impact genes important for neuronal function. We identify aspects of the single-cell sequencing approach, bioinformatic analysis, and validation methods that led to thousands of artifacts being interpreted as somatic mutation events. Our reanalysis supports a mutation frequency of approximately 0.2 events per cell, which is about fifty-fold lower than reported, confirming that L1 elements mobilize in some human neurons but indicating that L1 mosaicism is not ubiquitous. Through consideration of the challenges identified, we provide a foundation and framework for designing single-cell genomics studies.


2013 ◽  
pp. 83-88 ◽  
Author(s):  
Martin Ingvar ◽  
Predrag Petrovic ◽  
Karin Jensen

2017 ◽  
Vol 39 (04) ◽  
pp. 261-270
Author(s):  
Daniel Damiani ◽  
Anna Maria Nascimento ◽  
Leticia Kühl Pereira

AbstractIn 1909, Korbinian Brodmann described 52 functional brain areas, 43 of them found in the human brain. More than a century later, his devoted functional map was incremented by Glasser et al in 2016, using functional nuclear magnetic resonance imaging techniques to propose the existence of 180 functional areas in each hemisphere, based on their cortical thickness, degree of myelination (cortical myelin content), neuronal interconnection, topographic organization, multitask answers, and assessment in their resting state. This opens a huge possibility, through functional neuroanatomy, to understand a little more about normal brain function and its functional impairment in the presence of a disease.


Sign in / Sign up

Export Citation Format

Share Document