Skip to main content
Intended for healthcare professionals
Free access
Research article
First published May 1969

THE CYTOCHEMISTRY AND ULTRASTRUCTURE OF POLYPEPTIDE HORMONE-PRODUCING CELLS OF THE APUD SERIES AND THE EMBRYOLOGIC, PHYSIOLOGIC AND PATHOLOGIC IMPLICATIONS OF THE CONCEPT

Abstract

A group of apparently unrelated endocrine cells, some in endocrine glands, others in nonendocrine tissues, share a number of cytochemical and ultrastructural characteristics. These characteristics, from the initial letters of four of which the term APUD is derived, indicate the possession of a common metabolic pattern and common synthetic, storage and secretion mechanisms. It is postulated that the various characteristics reflect the production and storage of hormone precursor protein which has a predominantly random coil conformation. Several explanations are possible to account for the APUD characteristics but if the cells, in fact, share a common ancestor the only possible candidate is the neural crest cell.

Cite

Cite

Cite

OR

Download to reference manager

If you have citation software installed, you can download citation data to the citation manager of your choice

Share options

Share

Share this publication

Share with email
Email Link
Share on social media

Share access to this article

Sharing links are not relevant where the article is open access and not available if you do not have a subscription.

For more information view the Sage Journals article sharing page.

Information, rights and permissions

Information

Published In

Article first published: May 1969
Issue published: May 1969

Rights and permissions

1969, THE HISTOCHEMICAL SOCIETY, INC.
Request permissions for this article.
PubMed: 4143745

Authors

Affiliations

A. G. E. PEARSE
Royal postgraduate Medical School, London, England

Metrics and citations

Metrics

Journals metrics

This article was published in Journal of Histochemistry & Cytochemistry.

View All Journal Metrics

Publication usage*

Total views and downloads: 1092

*Usage tracking began in December 2016 or upon migration to Sage Journals, whichever is later. Prior usage data was not transferred.


Publications citing this one

Receive email alerts when this publication is cited

Web of Science: 1685 view articles Opens in new tab

Crossref: 1303

  1. Mechanistic insights and molecular therapy for neuroendocrine prostate cancer
    Go to citationCrossrefGoogle Scholar
  2. Neuroendocrine Neoplasia
    Go to citationCrossrefGoogle Scholar
  3. Diabetes and Alzheimer's Disease
    Go to citationCrossrefGoogle Scholar
  4. Paraneurons
    Go to citationCrossrefGoogle Scholar
  5. Neuroendocrine Neoplasia
    Go to citationCrossrefGoogle Scholar
  6. How the diffuse neuroendocrine system shapes health, homeostasis, and cancer
    Go to citationCrossrefGoogle Scholar
  7. Proneural gene Mash1 (Ascl1) is expressed in multiple lineages and regulates their differentiation and specification
    Go to citationCrossrefGoogle Scholar
  8. Serotonin Signaling and Macrophage Subsets in Goldfish Gills: Unraveling the Neuroimmune Network for Gill Homeostasis
    Go to citationCrossrefGoogle Scholar
  9. Analysis of Amyloid Using Various Methods
    Go to citationCrossrefGoogle Scholar
  10. Peptide Receptor Radionuclide Therapy in Lung and Mediastinum Neuroendocrine Tumor
    Go to citationCrossrefGoogle Scholar
  11. View More

Figures and tables

Figures & Media

Tables

View Options

View options

PDF/EPUB

View PDF/EPUB

Access options

If you have access to journal content via a personal subscription, university, library, employer or society, select from the options below:

JHC members can access this journal content using society membership credentials.

JHC members can access this journal content using society membership credentials.


Alternatively, view purchase options below:

Purchase 24 hour online access to view and download content.

Access journal content via a DeepDyve subscription or find out more about this option.

Morty Proxy This is a proxified and sanitized view of the page, visit original site.