Three-dimensional visualization of osteoclasts in embryonic mouse mandibles using SEM array tomography

Author(s):  
Liao Caiyu ◽  
Megumi Nakamura ◽  
Miyuki Mayanagi ◽  
Atsuko Kayaba ◽  
Yasuyuki Sasano
2010 ◽  
Vol 2010 (11) ◽  
pp. pdb.top89-pdb.top89 ◽  
Author(s):  
K. D. Micheva ◽  
N. O'Rourke ◽  
B. Busse ◽  
S. J. Smith

2001 ◽  
Vol 158 (1) ◽  
pp. 49-55 ◽  
Author(s):  
Carrie L. Phillips ◽  
Lois J. Arend ◽  
Adele J. Filson ◽  
Doug J. Kojetin ◽  
Jeffrey L. Clendenon ◽  
...  

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Gerald J. Shami ◽  
Delfine Cheng ◽  
Pauline Verhaegh ◽  
Ger Koek ◽  
Eddie Wisse ◽  
...  

AbstractGiant mitochondria are peculiarly shaped, extremely large mitochondria in hepatic parenchymal cells, the internal structure of which is characterised by atypically arranged cristae, enlarged matrix granules and crystalline inclusions. The presence of giant mitochondria in human tissue biopsies is often linked with cellular adversity, caused by toxins such as alcohol, xenobiotics, anti-cancer drugs, free-radicals, nutritional deficiencies or as a consequence of high fat Western diets. To date, non-alcoholic fatty liver disease is the most prevalent liver disease in lipid dysmetabolism, in which mitochondrial dysfunction plays a crucial role. It is not well understood whether the morphologic characteristics of giant mitochondria are an adaption or caused by such dysfunction. In the present study, we employ a complementary multimodal imaging approach involving array tomography and transmission electron tomography in order to comparatively analyse the structure and morphometric parameters of thousands of normal- and giant mitochondria in four patients diagnosed with non-alcoholic fatty liver disease. In so doing, we reveal functional alterations associated with mitochondrial gigantism and propose a mechanism for their formation based on our ultrastructural findings.


2017 ◽  
Vol 474 (9) ◽  
pp. 1495-1508 ◽  
Author(s):  
Sarah M. Smith ◽  
Andrew Yarwood ◽  
Roland A. Fleck ◽  
Colin Robinson ◽  
Corinne J. Smith

The twin-arginine translocation (Tat) system is an integral membrane protein complex that accomplishes the remarkable feat of transporting large, fully folded polypeptides across the inner membrane of bacteria, into the periplasm. In Escherichia coli, Tat comprises three membrane proteins: TatA, TatB and TatC. How these proteins arrange themselves in the inner membrane to permit passage of Tat substrates, whilst maintaining membrane integrity, is still poorly understood. TatA is the most abundant component of this complex and facilitates assembly of the transport mechanism. We have utilised immunogold labelling in combination with array tomography to gain insight into the localisation and distribution of the TatA protein in E. coli cells. We show that TatA exhibits a uniform distribution throughout the inner membrane of E. coli and that altering the expression of TatBC shows a previously uncharacterised distribution of TatA in the inner membrane. Array tomography was used to provide our first insight into this altered distribution of TatA in three-dimensional space, revealing that this protein forms linear clusters in the inner membrane of E. coli upon increased expression of TatBC. This is the first indication that TatA organisation in the inner membrane alters in response to changes in Tat subunit stoichiometry.


2011 ◽  
Vol 4 (2) ◽  
pp. 311-323 ◽  
Author(s):  
Sanaz Saatchi ◽  
Nishey Wanchoo ◽  
Junya Azuma ◽  
Stephen J Smith ◽  
Philip S. Tsao ◽  
...  

Author(s):  
Jan Philipp Schneider ◽  
Jan Hegermann ◽  
Christoph Wrede

AbstractSince its entry into biomedical research in the first half of the twentieth century, electron microscopy has been a valuable tool for lung researchers to explore the lung’s delicate ultrastructure. Among others, it proved the existence of a continuous alveolar epithelium and demonstrated the surfactant lining layer. With the establishment of serial sectioning transmission electron microscopy, as the first “volume electron microscopic” technique, electron microscopy entered the third dimension and investigations of the lung’s three-dimensional ultrastructure became possible. Over the years, further techniques, ranging from electron tomography over serial block-face and focused ion beam scanning electron microscopy to array tomography became available. All techniques cover different volumes and resolutions, and, thus, different scientific questions. This review gives an overview of these techniques and their application in lung research, focusing on their fields of application and practical implementation. Furthermore, an introduction is given how the output raw data are processed and the final three-dimensional models can be generated.


2018 ◽  
Vol 24 (S1) ◽  
pp. 1248-1249
Author(s):  
M. Suga ◽  
H. Nisioka ◽  
M. Nakamura ◽  
K. Suzuki ◽  
K. Konishi ◽  
...  

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