Literature DB >> 8906502

Increased cerebellar Purkinje cell numbers in mice overexpressing a human bcl-2 transgene.

H S Zanjani1, M W Vogel, N Delhaye-Bouchaud, J C Martinou, J Mariani.   

Abstract

The Purkinje cell is a primary organizer in the development of the cerebellum. Purkinje cells may provide positional information cues that regulate afferent innervation, and Purkinje cell target size controls the adult number of afferent olivary neurons and granule cells. While Purkinje cells are necessary for the survival of olivary neurons and granule cells during periods of programmed cell death, little is known about the survival requirements of Purkinje cells in vivo. To determine if Purkinje cells are subject to programmed cell death during development we have analyzed Purkinje cell numbers in two lines of transgenic mice that overexpress a human gene for bcl-2 (Hu-bcl-2). Bcl-2 is a protooncogene that inhibits apoptosis in many cell types. Overexpression of bcl-2 in vitro and in vivo rescues neurons from trophic factor deprivation or naturally occurring cell death. In the mice analyzed in this study, transgene expression is driven by the neuron-specific enolase promoter that is first expressed embryonically in most regions of the brain in one line and postnatally in the second line. We have counted Purkinje cells in three adult control mice, five early overexpressing transgenics, and three late expressing transgenics. The number of Purkinje cells in the Hu-bcl-2 transgenic mice is significantly increased above control numbers, with an increase of 43% in the embryonically overexpressing line and an increase of 27% in the postnatally overexpressing line. Because bcl-2 overexpression has been shown to rescue other neurons from programmed cell death, the increase in Purkinje cell numbers in overexpressing bcl-2 transgenics suggests that Purkinje cells undergo a period of cell death during normal development.

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Year:  1996        PMID: 8906502     DOI: 10.1002/(SICI)1096-9861(19961021)374:3<332::AID-CNE2>3.0.CO;2-2

Source DB:  PubMed          Journal:  J Comp Neurol        ISSN: 0021-9967            Impact factor:   3.215


  18 in total

Review 1.  Cell death as a regulator of cerebellar histogenesis and compartmentation.

Authors:  Jakob Jankowski; Andreas Miething; Karl Schilling; John Oberdick; Stephan Baader
Journal:  Cerebellum       Date:  2011-09       Impact factor: 3.847

2.  Physiological purkinje cell death is spatiotemporally organized in the developing mouse cerebellum.

Authors:  Jakob Jankowski; Andreas Miething; Karl Schilling; Stephan L Baader
Journal:  Cerebellum       Date:  2009-02-24       Impact factor: 3.847

3.  A hybrid nanofiber matrix to control the survival and maturation of brain neurons.

Authors:  Shantanu Sur; Eugene T Pashuck; Mustafa O Guler; Masao Ito; Samuel I Stupp; Thomas Launey
Journal:  Biomaterials       Date:  2011-10-20       Impact factor: 12.479

4.  Transplantation of mouse embryonic stem cells into the cochlea of an auditory-neuropathy animal model: effects of timing after injury.

Authors:  Hainan Lang; Bradley A Schulte; John C Goddard; Michelle Hedrick; Jason B Schulte; Ling Wei; Richard A Schmiedt
Journal:  J Assoc Res Otolaryngol       Date:  2008-05-01

Review 5.  The mysterious microcircuitry of the cerebellar nuclei.

Authors:  Marylka Uusisaari; Erik De Schutter
Journal:  J Physiol       Date:  2011-04-26       Impact factor: 5.182

6.  Maternal immune activation produces cerebellar hyperplasia and alterations in motor and social behaviors in male and female mice.

Authors:  Tooka Aavani; Shadna A Rana; Richard Hawkes; Quentin J Pittman
Journal:  Cerebellum       Date:  2015-10       Impact factor: 3.847

7.  Local insulin-like growth factor I expression is essential for Purkinje neuron survival at birth.

Authors:  L Croci; V Barili; D Chia; L Massimino; R van Vugt; G Masserdotti; R Longhi; P Rotwein; G G Consalez
Journal:  Cell Death Differ       Date:  2010-07-02       Impact factor: 15.828

8.  Insulin-like growth factor-I overexpression attenuates cerebellar apoptosis by altering the expression of Bcl family proteins in a developmentally specific manner.

Authors:  D Chrysis; A S Calikoglu; P Ye; A J D'Ercole
Journal:  J Neurosci       Date:  2001-03-01       Impact factor: 6.167

9.  c-Jun N-terminal kinase (JNK) and p38 play different roles in age-related Purkinje cell death in murine organotypic culture.

Authors:  Mariaelena Repici; Rosine Wehrlé; Xanthi Antoniou; Tiziana Borsello; Isabelle Dusart
Journal:  Cerebellum       Date:  2011-06       Impact factor: 3.847

Review 10.  Cell death, Bcl-2, Bax, and the cerebellum.

Authors:  Michael W Vogel
Journal:  Cerebellum       Date:  2002-12       Impact factor: 3.847

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