Dense-core granules

A specific hallmark of the neuronal/neurosecretory cell phenotype

Maria Luisa Malosio, Tiziana Giordano, Andrea Laslop, Jacopo Meldolesi

Research output: Contribution to journalArticle

55 Citations (Scopus)

Abstract

Expression of dense-core granules, a typical exocytic organelle, is widely believed to be controlled by coordinate gene expression mechanisms specific to neurones and neurosecretory cells. Recent studies in PC12 cells, however, have suggested the number of granules/cells depends on the levels of only one of their cargo proteins, chromogranin A, regulating the metabolism of the other proteins, and thus the composition of the organelles, by an on/off switch mechanism. In addition, transfection of chromogranin A was reported to induce appearance of dense-core granules in the non-neurosecretory fibroblasts of the CV-1 line. Here the role of chromogranin A has been reinvestigated using not the heterogeneous PC12 line but several clones isolated therefrom. In these clones, investigated as such or after transfection with chromogranin A antisense sequences, the ratio between chromogranin A and its secretory protein mate, chromogranin B, was not constant but highly and apparently randomly variable. Variability of the chromogranin A/chromogranin B ratio was seen by confocal immunofluorescence also among the cells of single clones and subclones and among the granules of single cells. Moreover, stable and transient transfections of chromogranin A in a PC12 clone characterised by a low number of dense-core granules (one fifth of the reference clone) failed to modify significantly the number of the organelles, despite the several-fold increase of the granin. Finally, in three types of non-neurosecretory cells (CV-1, adenocarcinoma TS/A and a clone of PC12 incompetent for secretion) the transfected chromogranin A accumulated mostly in the Golgi/transGolgi area and was released rapidly from resting cells (constitutive secretion) as revealed by both immunofluorescence during cycloheximide treatment and pulse-chase experiments. Only a minor fraction was sorted to discrete organelles that were not dense-core granules, but primarily lysosomes because they contained no chromogranin B, and were largely positive for the late endosomal-lysosomal markers, lamp1 and lamp3. Dense-core granules are therefore true hallmarks of neurones and neurosecretory cells. Their number/cell appears independent of chromogranin A and their composition does not appear to be constant; in particular, they exhibit considerable, and so far unexplained variability in the chromogranin A/chromogranin B ratio.

Original languageEnglish
Pages (from-to)743-749
Number of pages7
JournalJournal of Cell Science
Volume117
Issue number5
DOIs
Publication statusPublished - Feb 15 2004

Fingerprint

Chromogranin A
Phenotype
Chromogranin B
Clone Cells
Organelles
Transfection
Fluorescent Antibody Technique
Cell Count
Chromogranins
Neurons
Proteins
PC12 Cells
Cycloheximide
Lysosomes
Adenocarcinoma
Fibroblasts
Gene Expression

Keywords

  • Chromogranin A
  • Chromogranin B
  • Dense-core granules
  • Neurosecretory cells
  • Regulated exocytoxis

ASJC Scopus subject areas

  • Cell Biology

Cite this

Dense-core granules : A specific hallmark of the neuronal/neurosecretory cell phenotype. / Malosio, Maria Luisa; Giordano, Tiziana; Laslop, Andrea; Meldolesi, Jacopo.

In: Journal of Cell Science, Vol. 117, No. 5, 15.02.2004, p. 743-749.

Research output: Contribution to journalArticle

Malosio, Maria Luisa ; Giordano, Tiziana ; Laslop, Andrea ; Meldolesi, Jacopo. / Dense-core granules : A specific hallmark of the neuronal/neurosecretory cell phenotype. In: Journal of Cell Science. 2004 ; Vol. 117, No. 5. pp. 743-749.
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