Literature DB >> 1703294

Expression of a unique 56-kDa polypeptide by neurons in the subplate zone of the developing cerebral cortex.

J R Naegele1, C J Barnstable, P R Wahle.   

Abstract

In the mammalian cerebral cortex, neurons destined for layers 2-6 are generated only after the period of genesis for a group of transient neurons that populate the subplate and marginal zones. Although a number of molecular markers for the subplate zone exist, most are also expressed by other cell populations in the cortical plate. To begin to study molecular properties of the subplate, we generated monoclonal antibodies against homogenates of cat cortical subplate zone. One monoclonal antibody, termed subplate 1 (SP1), recognized a polypeptide of 56 kDa. This antigen was strongly expressed within the subplate neurons only during a 3-week period beginning at birth and extending until 3 weeks after birth. From postnatal day 1, the number of SP1-immunoreactive neurons below the visual cortex increased until the end of second postnatal week and then declined thereafter. This period coincides with the period when a majority of the subplate neurons undergo naturally occurring cell death. The antigen was not expressed by subplate neurons surviving in the adult white matter. At the peak of antigen expression, 14% or less of the immunoreactive neurons also coexpressed gamma-aminobutyric acid, somatostatin, or neuropeptide Y. Biochemical and immunocytochemical properties of the SP1 antigen were also compared with the Alz-50 antigen (A68), a marker for dying neurons. On Western blots, SP1- and Alz-50-reactive polypeptides were selectively enriched in cytosolic fractions of kitten cerebral cortex, but each marker recognized different molecular weight polypeptides. In tissue sections many subplate, cortical plate, and layer 1 neurons were Alz-50 immunoreactive. In contrast, a rarer subpopulation of neurons restricted to the subplate was labeled by SP1. We propose that the SP1 antigen is a protein expressed within dying cortical subplate neurons, at the commencement of cell death.

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Year:  1991        PMID: 1703294      PMCID: PMC50804          DOI: 10.1073/pnas.88.2.330

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  38 in total

1.  O-acetylation of a cell-surface carbohydrate creates discrete molecular patterns during neural development.

Authors:  A S Blum; C J Barnstable
Journal:  Proc Natl Acad Sci U S A       Date:  1987-12       Impact factor: 11.205

2.  Subplate neurons pioneer the first axon pathway from the cerebral cortex.

Authors:  S K McConnell; A Ghosh; C J Shatz
Journal:  Science       Date:  1989-09-01       Impact factor: 47.728

3.  Selective staining of a subset of GABAergic neurons in cat visual cortex by monoclonal antibody VC1.1.

Authors:  J R Naegele; Y Arimatsu; P Schwartz; C J Barnstable
Journal:  J Neurosci       Date:  1988-01       Impact factor: 6.167

4.  Molecular markers of neuronal subpopulations in layers 4, 5, and 6 of cat primary visual cortex.

Authors:  Y Arimatsu; J R Naegele; C J Barnstable
Journal:  J Neurosci       Date:  1987-04       Impact factor: 6.167

5.  Postnatal maturation of nonpyramidal neurons in the visual cortex of the cat.

Authors:  G Meyer; R Ferres-Torres
Journal:  J Comp Neurol       Date:  1984-09-10       Impact factor: 3.215

6.  Ontogenesis of microtubule-associated protein 2 (MAP2) in embryonic mouse cortex.

Authors:  J E Crandall; M Jacobson; K S Kosik
Journal:  Brain Res       Date:  1986-07       Impact factor: 3.252

7.  Morphology and axon terminal pattern of glutamate decarboxylase-immunoreactive cell types in the white matter of the cat occipital cortex during early postnatal development.

Authors:  P Wahle; G Meyer; J Y Wu; K Albus
Journal:  Brain Res       Date:  1987-11       Impact factor: 3.252

8.  Transient cells of the developing mammalian telencephalon are peptide-immunoreactive neurons.

Authors:  J J Chun; M J Nakamura; C J Shatz
Journal:  Nature       Date:  1987 Feb 12-18       Impact factor: 49.962

9.  Alzheimer-related neuronal protein A68: specificity and distribution.

Authors:  B Wolozin; P Davies
Journal:  Ann Neurol       Date:  1987-10       Impact factor: 10.422

10.  Alz-50, ubiquitin and tau immunoreactivity of neurofibrillary tangles, Pick bodies and Lewy bodies.

Authors:  S Love; T Saitoh; S Quijada; G M Cole; R D Terry
Journal:  J Neuropathol Exp Neurol       Date:  1988-07       Impact factor: 3.685

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  7 in total

1.  Distribution of neurons expressing substance P receptor messenger RNA in immature and adult cat visual cortex.

Authors:  C Matute; P Wahle; K Gutiérrez-Igarza; K Albus
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2.  Maternally derived immunoglobulin light chain is present in the fetal mammalian CNS.

Authors:  J A Weiner; J Chun
Journal:  J Neurosci       Date:  1997-05-01       Impact factor: 6.167

3.  Morphology of neurons in the white matter of the adult human neocortex.

Authors:  G Meyer; P Wahle; A Castaneyra-Perdomo; R Ferres-Torres
Journal:  Exp Brain Res       Date:  1992       Impact factor: 1.972

Review 4.  Immunoglobulin expression in non-lymphoid lineage and neoplastic cells.

Authors:  Zhengshan Chen; Xiaoyan Qiu; Jiang Gu
Journal:  Am J Pathol       Date:  2009-02-26       Impact factor: 4.307

5.  A biphasic pattern of gene expression during mouse retina development.

Authors:  Samuel Shao-Min Zhang; Xuming Xu; Mu-Gen Liu; Hongyu Zhao; Marcelo Bento Soares; Colin J Barnstable; Xin-Yuan Fu
Journal:  BMC Dev Biol       Date:  2006-10-17       Impact factor: 1.978

6.  Expression of immunoglobulin constant domain genes in neurons of the mouse central nervous system.

Authors:  Louis Scheurer; Rebecca R Das Gupta; Annika Saebisch; Thomas Grampp; Dietmar Benke; Hanns Ulrich Zeilhofer; Hendrik Wildner
Journal:  Life Sci Alliance       Date:  2021-08-25

Review 7.  Cornu Ammonis Regions-Antecedents of Cortical Layers?

Authors:  Audrey Mercer; Alex M Thomson
Journal:  Front Neuroanat       Date:  2017-09-26       Impact factor: 3.856

  7 in total

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