Literature DB >> 14964684

Distribution of calcium-binding proteins in the cerebellum.

Enrico Bastianelli1.   

Abstract

Calcium plays a fundamental role in the cell as second messenger and is principally regulated by calcium-binding proteins. Although these proteins share in common their ability to bind calcium, they belong to different subfamilies. They present, in general, specific developmental and distribution patterns. Most Purkinje cells express the fast and slow calcium buffer proteins calbindin-D28k and parvalbumin, whereas basket, stellate and Golgi cells the slow buffer parvalbumin only. They are, almost all, calretinin negative. Granule, Lugaro and unipolar brush cells present an opposite immunoreactivity profile, most of them being calretinin positive while lacking calbindin-D28k and parvalbumin. The developmental pattern of appearance of these proteins seems to follow the maturation of neurons. Calbindin-D28k appears early, shortly after cessation of mitosis when neurons become ready to start migration and differentiation while parvalbumin is expressed later in parallel with an increase in neuronal activity. The other proteins are generally detected later. During development, some of these proteins, like calretinin, are transiently expressed in specific cellular subpopulations. The function of these proteins is not fully understood, although strong evidence supports a prominent role in physiological settings with altered calcium concentrations. These proteins regulate and are regulated by intracellular calcium level. For example, they may directly or indirectly enable sensitization or desensitization of calcium channels, and may further block calcium entry into the cells, like the calcium-sensor proteins, that have been shown to be potent and specific modulators of ion channels, which may allow for feedback control of current function and hence signaling. The absence of calcium buffer proteins results in marked abnormalities in cell firing; with alterations in simple and complex spikes or transformation of depressing synapses into facilitating synapses. Calcium-binding protein implication in resistance to degeneration is still a controversial issue. Neurons rich in calcium-binding proteins, especially calbindin-D28k and parvalbumin, seem to be relatively resistant to degeneration in a variety of acute and chronic disorders. However other data support that an absence of calcium-binding proteins may also have a neuroprotective effect. It is not unlikely that neurons may face a dual action mechanism where a decrease in calcium-binding proteins has a first short-term beneficial effect while it becomes detrimental for the cell over the long term.

Entities:  

Mesh:

Substances:

Year:  2003        PMID: 14964684     DOI: 10.1080/14734220310022289

Source DB:  PubMed          Journal:  Cerebellum        ISSN: 1473-4222            Impact factor:   3.847


  132 in total

Review 1.  Classification and evolution of EF-hand proteins.

Authors:  H Kawasaki; S Nakayama; R H Kretsinger
Journal:  Biometals       Date:  1998-12       Impact factor: 2.949

Review 2.  Structure of the human cDNAs and genes coding for calbindin D28K and calretinin.

Authors:  M Parmentier
Journal:  Adv Exp Med Biol       Date:  1990       Impact factor: 2.622

3.  Opposite regulation of calbindin and calretinin expression by brain-derived neurotrophic factor in cortical neurons.

Authors:  H Fiumelli; M Kiraly; A Ambrus; P J Magistretti; J L Martin
Journal:  J Neurochem       Date:  2000-05       Impact factor: 5.372

Review 4.  Evolutionary diversification of structure and function in the family of intracellular calcium-binding proteins.

Authors:  M Goodman; J F Pechère; J Haiech; J G Demaille
Journal:  J Mol Evol       Date:  1979-11       Impact factor: 2.395

5.  Localization of the neural calcium-binding protein VILIP (visinin-like protein) in neurons of the chick visual system and cerebellum.

Authors:  S E Lenz; S Jiang; K Braun; E D Gundelfinger
Journal:  Cell Tissue Res       Date:  1996-03       Impact factor: 5.249

6.  Overexpression of calbindin-D28K induces neurite outgrowth in dopaminergic neuronal cells via activation of p38 MAPK.

Authors:  W S Choi; S Y Chun; G J Markelonis; T H Oh; Y J Oh
Journal:  Biochem Biophys Res Commun       Date:  2001-09-28       Impact factor: 3.575

7.  Changes in shape and motility of cells transfected with parvalbumin cDNA.

Authors:  C Andressen; V Gotzos; M W Berchtold; T L Pauls; B Schwaller; B Fellay; M R Celio
Journal:  Exp Cell Res       Date:  1995-08       Impact factor: 3.905

8.  Staggerer mutant mouse Purkinje cells do not contain detectable calmodulin mRNA.

Authors:  A Messer; J Plummer-Siegard; B Eisenberg
Journal:  J Neurochem       Date:  1990-07       Impact factor: 5.372

9.  Process of differentiation of cerebellar Purkinje neurons in the chick embryo.

Authors:  M Bertossi; L Roncali; L Mancini; D Ribatti; B Nico
Journal:  Anat Embryol (Berl)       Date:  1986

10.  Parvalbumin is a marker of ALS-resistant motor neurons.

Authors:  J L Elliott; W D Snider
Journal:  Neuroreport       Date:  1995-02-15       Impact factor: 1.837

View more
  78 in total

1.  Rebound from Inhibition: Self-Correction against Neurodegeneration?

Authors:  Shobhana Sivaramakrishnan; William P Lynch
Journal:  J Clin Cell Immunol       Date:  2017-03-13

Review 2.  Of mice and rats: key species variations in the sexual differentiation of brain and behavior.

Authors:  P J Bonthuis; K H Cox; B T Searcy; P Kumar; S Tobet; E F Rissman
Journal:  Front Neuroendocrinol       Date:  2010-05-10       Impact factor: 8.606

3.  Suppression of calbindin-D28k expression exacerbates SCA1 phenotype in a disease mouse model.

Authors:  Parminder J S Vig; Jinrong Wei; Qingmei Shao; Maripar E Lopez; Rebecca Halperin; Jill Gerber
Journal:  Cerebellum       Date:  2012-09       Impact factor: 3.847

4.  Changes induced by natural scrapie in the calretinin-immunopositive cells and fibres of the sheep cerebellar cortex.

Authors:  Adolfo Toledano; María-Isabel Alvarez; Eva Monleón; Adolfo Toledano-Díaz; Juan-José Badiola; Marta Monzón
Journal:  Cerebellum       Date:  2012-06       Impact factor: 3.847

Review 5.  Models of calcium dynamics in cerebellar granule cells.

Authors:  Elena È Saftenku
Journal:  Cerebellum       Date:  2012-03       Impact factor: 3.847

6.  Sources of calretinin inputs to motoneurons of extraocular muscles involved in upgaze.

Authors:  Julia Ahlfeld; Michael Mustari; Anja K E Horn
Journal:  Ann N Y Acad Sci       Date:  2011-09       Impact factor: 5.691

7.  Ca(2+) current facilitation determines short-term facilitation at inhibitory synapses between cerebellar Purkinje cells.

Authors:  Françoise Díaz-Rojas; Takeshi Sakaba; Shin-Ya Kawaguchi
Journal:  J Physiol       Date:  2015-10-12       Impact factor: 5.182

8.  Apoptosis inducing factor deficiency causes reduced mitofusion 1 expression and patterned Purkinje cell degeneration.

Authors:  Seung-Hyuk Chung; Marco Calafiore; Jennifer M Plane; David E Pleasure; Wenbin Deng
Journal:  Neurobiol Dis       Date:  2010-10-23       Impact factor: 5.996

9.  Processing of the matricellular protein hevin in mouse brain is dependent on ADAMTS4.

Authors:  Matt S Weaver; Gail Workman; Marina Cardo-Vila; Wadih Arap; Renata Pasqualini; E Helene Sage
Journal:  J Biol Chem       Date:  2009-12-15       Impact factor: 5.157

10.  Maternal Exposure to Valproic Acid Primarily Targets Interneurons Followed by Late Effects on Neurogenesis in the Hippocampal Dentate Gyrus in Rat Offspring.

Authors:  Yousuke Watanabe; Tomoaki Murakami; Masashi Kawashima; Yasuko Hasegawa-Baba; Sayaka Mizukami; Nobuya Imatanaka; Yumi Akahori; Toshinori Yoshida; Makoto Shibutani
Journal:  Neurotox Res       Date:  2016-08-26       Impact factor: 3.911

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.