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Ultrastructural changes in pancreatic beta cells treated with NGF and dbcAMP

  • M. González del Pliegob(Author)
    ,
  • E. Aguirre-Benítezb(Author)
    ,
  • M. Del Carmen Sánchez-Sotoa(Author)
    ,
  • M. Larrietaa(Author)
    ,
  • A. Velázquez-Carranzab(Author)
    ,
  • aInstituto de Fisiologia Celular de la UNAM
    ,
  • bUniversidad de Colima, Facultad de Medicina
Research Output: Contribution to journal Article Peer-review

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0.55
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10
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10
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60

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Abstract

Nerve growth factor (NGF) induces morphological and physiological changes in cultured pancreatic β-cells, including the extension of neurite-like processes. This latter effect is potentiated by dibutyryl cAMP (dbcAMP). β-cells cultured under these conditions maintain their immunoreactivity to insulin and gamma-amino-butyric acid (GABA). NGF, dbcAMP, and high glucose concentrations also increase the expression of the GABA-synthesizing enzyme glutamic acid decarboxylase-65 in cultured β-cells. The aim of this work was to study the effect of NGF alone or in combination with dbcAMP on pancreatic β-cell ultrastructural morphology, after 10 days in culture. We used light microscopy, scanning electron microscopy, and transmission electron microscopy to analyze the modifications in cell surface and neurite-like projections. Morphometric analysis showed that NGF and/or dbcAMP treatment substantially increased the insulin and GABA content in granules and rough endoplasmic reticulum. Given that pancreatic β-cells express NGF receptors and that NGF is synthesized and secreted by β-cells, these results further suggest that NGF could have trophic actions on pancreatic hormone synthesis and/or storage.

Publication Information

Output type

Research Output: Contribution to journal Article Peer-review

Original language

English

Pages from-to (Number of pages)

Pages 365-378 (14 pages)

Journal (Volume, Issue Number)

Cell and Tissue Research (Volume 305, Issue 3)

Publication milestones

  • Published - 01/12/2001

Publication status

Published - 01/12/2001

ISSN

0302-766X

External Publication IDs

  • Scopus: 18344376701