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ELECTRON MICROSCOPY OF THE HUMAN SYNOVIAL MEMBRANE

Peter Barland1,Alex B Novikoff1,David Hamerman1
1From the Departments of Pathology and Medicine, Albert Einstein College of Medicine, New York

Received 1962 Jan 5.

Copyright © Copyright, 1962, by The Rockefeller Institute Press

This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (seehttp://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described athttp://creativecommons.org/licenses/by-nc-sa/4.0/).

PMCID: PMC2106097  PMID:13865038

Abstract

The structure of the lining cells at the surface of the synovial membrane facing the joint cavity has been studied by electron microscopy. The long cytoplasmic processes of these cells appear to be oriented toward the surface of the membrane, where they overlap and intertwine. The matrix of the lining cells contains dense material but no fibers with the periodicity of collagen. The lining cells are divided into two cell types or states of activity on the basis of their cytoplasmic contents. Type A is more numerous and contains a prominent Golgi apparatus, numerous vacuoles (0.4 to 1.5 microns in diameter) containing varying amounts of a dense granular material, many filopodia, mitochondria, intracellular fibrils, and micropinocytotic-like vesicles. Type B contains large amounts of ergastoplasm with fewer large vacuoles, micropinocytotic-like vesicles, and mitochondria. The probable functions of these cells are discussed in the light of current knowledge of the metabolism and function of the synovial membrane.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

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Articles from The Journal of Cell Biology are provided here courtesy ofThe Rockefeller University Press

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