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P. Lea, R. Temkin, K. Freeman, Grant Mitchell, Brain Robinson (1994)
Variations in mitochondrial ultrastructure and dynamics observed by high resolution scanning electron microscopy (HRSEM)Microscopy Research and Technique, 27
C. Zancanaro, V. Carnielli, C. Moretti, D. Benati, P. Gamba (1995)
An ultrastructural study of brown adipose tissue in pre-term human new-borns.Tissue & cell, 27 3
D. Lončar (1990)
Immunoelectron microscopical studies on synthesis and localization of uncoupling protein in brown adipocytes: evidence for cotranslational transport of uncoupling protein into mitochondria.Journal of structural biology, 105 1-3
P. Ruiz‐Lozano, Susan Smith, G. Perkins, S. Kubalak, G. Boss, H. Sucov, R. Evans, K. Chien (1998)
Energy deprivation and a deficiency in downstream metabolic target genes during the onset of embryonic heart failure in RXRalpha-/- embryos.Development, 125 3
N. Pfanner, J. Rassow, I. Klei, W. Neupert (1992)
A dynamic model of the mitochondrial protein import machineryCell, 68
A. Bakker, F. Goossens, M. Bie, I. Bernaert, H. Belle, W. Jacob (1995)
The effect of ischemia and reperfusion on mitochondrial contact sites in isolated rat hearts.Histology and histopathology, 10 2
von Ml, S. Fakan, W. Villiger, M. Müller (1993)
Cryofixation and cryosubstitution: a useful alternative in the analyses of cellular fine structure.European journal of histochemistry : EJH, 37 1
S. Malhotra, J. Tewari (1991)
Contact sites between mitochondrial membranes: comments.Cytobios, 68 273
H. Dalen, M. Lieberman, A. Lefurgey, P. Scheie, J. Sommer (1992)
Quick‐freezing of cultured cardiac cells in situ with special attention to the mitochondrial ultrastructureJournal of Microscopy, 168
H. Hohenberg, M. Tobler, Martin Müller (1996)
High‐pressure freezing of tissue obtained by fine‐needle biopsyJournal of Microscopy, 183
C. Mannella, M. Marko, P. Penczek, D. Barnard, J. Frank (1994)
The internal compartmentation of rat‐liver mitochondria: Tomographic study using the high‐voltage transmission electron microscopeMicroscopy Research and Technique, 27
A. Glauert (1975)
Fixation, dehydration and embedding of biological specimens
G. Perkins, C. Renken, J. Song, T. Frey, S. Young, S. Lamont, M. Martone, S. Lindsey, Mark Ellisman (1997)
Electron tomography of large, multicomponent biological structures.Journal of structural biology, 120 3
H. Dalen, P. Scheie, R. Nassar, T. High, B. Scherer, I. Taylor, N. Wallace, J. Sommer (1992)
Cryopreservation evaluated with mitochondrial and Z line ultrastructure in striated muscleJournal of Microscopy, 165
K. Fujimoto, M. Umeda, T. Fujimoto (1996)
Transmembrane phospholipid distribution revealed by freeze-fracture replica labeling.Journal of cell science, 109 ( Pt 10)
W. Jacob, A. Bakker, R. Hertsens, W. Biermans (1994)
Mitochondrial matrix granules: Their behavior during changing metabolic situations and their relationship to contact sites between inner and outer mitochondrial membranesMicroscopy Research and Technique, 27
T. Creighton (1999)
Encyclopedia of molecular biology.
Electron microscope tomography was used to examine the membrane topology of brown adipose tissue (BAT) mitochondria prepared by cryofixation or chemical fixation techniques. These mitochondria contain an uncoupling protein which results in the conversion of energy from electron transport into heat. The three-dimensional reconstructions of BAT mitochondria provided a view of the inner mitochondrial membrane different in important features from descriptions found in the literature. The work reported here provides new insight into BAT mitochondria architecture by identifying crista junctions, including multiple junctions connecting a crista to the same side of the inner boundary membrane, in a class of mitochondria that have no tubular cristae, but only lamellar cristae. Crista junctions were defined previously as the tubular membranes of relatively uniform diameter that connect a crista membrane with the inner boundary membrane. We have also found that the cristae architecture of cryofixed mitochondria, including crista junctions, is similar to that found in chemically fixed mitochondria, suggesting that this architecture is not a fixation artifact. The stacks of lamellar cristae extended through more of the BAT mitochondrial volume than did the cristae we observed in neuronal mitochondria. Hence, the inner membrane surface area was larger in the former. In chemically fixed mitochondria, contact sites were easily visualized because the outer and inner boundary membranes were separated by an 8 nm space. However, in cryofixed mitochondria almost all the outer membrane was observed to be in close contact with the inner boundary membrane.
Journal of Bioenergetics and Biomembranes – Springer Journals
Published: Sep 28, 2004
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