Literature DB >> 2895815

Complementarity of particles and pits in freeze-fractured hepatic and cardiac gap junctions.

A M De Mazière1, D W Scheuermann, P A Aertgeerts.   

Abstract

Particles and pits of freeze-fractured gap junctions are considered as complementary structures despite the frequent observations of more regular and closer spacings of pits, ascribed to plastic deformation of particle arrays. Recently, however, the noncomplementarity of pits and particles in Purkinje fibers has been reported. To ascertain the relationship between both structures, gap junctions from fixed, cryoprotected liver and myocardium were investigated using spacing and density measurements and complementary replicas. In hepatocyte gap junctions, the center-to-center distances (mean +/- SD) among pits, 9.57 +/- 1.49 nm, and particles, 9.70 +/- 1.77 nm, are not significantly different. Density determinations yielded a slightly higher value for the pits, (11,510 +/- 830)/microns 2, than for the particles, (11,230 +/- 950)/microns 2. In the myocardium, the spacing of the regularly arrayed pits, 9.55 +/- 1.33 nm, barely exceeds the value of 9.44 +/- 1.62 nm for the particles, which show some clustering. However, the packing density for the pits, (10,090 +/- 740)/microns 2, appears a little higher than that of the particles, (9,890 +/- 920)/microns 2. As density and spacing measurements provided no decisive answers, the positions of individual pits and particles of complementary junctional faces were recorded on transparent sheets and compared. In this fashion, a one-to-one correspondence between particles and pits could be established, while small discrepancies may be attributed to plastic deformation. Moreover, the co-linearity of pits and particles may be suggested by the observation of a platinum grain in the center of many pits.

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Year:  1987        PMID: 2895815     DOI: 10.1007/bf01869417

Source DB:  PubMed          Journal:  J Membr Biol        ISSN: 0022-2631            Impact factor:   1.843


  27 in total

1.  Intercellular junctions and the cardiac intercalated disk.

Authors:  N J Severs
Journal:  Adv Myocardiol       Date:  1985

Review 2.  Junctional intercellular communication: the cell-to-cell membrane channel.

Authors:  W R Loewenstein
Journal:  Physiol Rev       Date:  1981-10       Impact factor: 37.312

3.  Structural correlates of glutaraldehyde induced uncoupling in mouse liver gap junctions.

Authors:  S Sikerwar; S Malhotra
Journal:  Eur J Cell Biol       Date:  1981-10       Impact factor: 4.492

Review 4.  Structural correlates of gap junction permeation.

Authors:  C Peracchia
Journal:  Int Rev Cytol       Date:  1980

5.  Particles and pits matched in native membranes.

Authors:  H P Ting-Beall; F M Burgess; J D Robertson
Journal:  J Microsc       Date:  1986-06       Impact factor: 1.758

6.  A modified cleansing procedure to obtain large freeze-fracture replicas.

Authors:  A M De Mazière; P Aertgeerts; D W Scheuermann
Journal:  J Microsc       Date:  1985-02       Impact factor: 1.758

7.  Differences between cytoplasmic surfaces of deep-etched heart and liver gap junctions.

Authors:  Y Shibata; C K Manjunath; E Page
Journal:  Am J Physiol       Date:  1985-09

8.  Freeze-fracturing in ultrahigh vacuum at -196 degrees C.

Authors:  H Gross; E Bas; H Moor
Journal:  J Cell Biol       Date:  1978-03       Impact factor: 10.539

9.  An interpretation of liver cell membrane and junction structure based on observation of freeze-fracture replicas of both sides of the fracture.

Authors:  J P Chalcroft; S Bullivant
Journal:  J Cell Biol       Date:  1970-10       Impact factor: 10.539

10.  Structure of rapidly frozen gap junctions.

Authors:  E Raviola; D A Goodenough; G Raviola
Journal:  J Cell Biol       Date:  1980-10       Impact factor: 10.539

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