scholarly journals Organization of the internal membrane system in the principal cells of the mouse epididymis after osmium impregnation

1988 ◽  
Vol 28 (5) ◽  
pp. 1237-1250 ◽  
Author(s):  
Marcelle-Anne FAIN-MAUREL ◽  
Aida ABOU-HAÏLA ◽  
J. P. DADOUNE
2017 ◽  
Vol 96 (2) ◽  
pp. 366-375 ◽  
Author(s):  
Yoo-Jin Park ◽  
Maria Agustina Battistone ◽  
Bongki Kim ◽  
Sylvie Breton

1983 ◽  
Vol 207 (2) ◽  
pp. 289-295 ◽  
Author(s):  
Kazuo Kanai ◽  
Shinsuke Kanamura ◽  
Jun Watanabe ◽  
Mari Asada-Kubota ◽  
Motoko Yoshikawa

eLife ◽  
2020 ◽  
Vol 9 ◽  
Author(s):  
Vera D Rinaldi ◽  
Elisa Donnard ◽  
Kyle Gellatly ◽  
Morten Rasmussen ◽  
Alper Kucukural ◽  
...  

Following testicular spermatogenesis, mammalian sperm continue to mature in a long epithelial tube known as the epididymis, which plays key roles in remodeling sperm protein, lipid, and RNA composition. To understand the roles for the epididymis in reproductive biology, we generated a single-cell atlas of the murine epididymis and vas deferens. We recovered key epithelial cell types including principal cells, clear cells, and basal cells, along with associated support cells that include fibroblasts, smooth muscle, macrophages and other immune cells. Moreover, our data illuminate extensive regional specialization of principal cell populations across the length of the epididymis. In addition to region-specific specialization of principal cells, we find evidence for functionally specialized subpopulations of stromal cells, and, most notably, two distinct populations of clear cells. Our dataset extends on existing knowledge of epididymal biology, and provides a wealth of information on potential regulatory and signaling factors that bear future investigation.


2017 ◽  
Vol 96 (4) ◽  
pp. 937-937 ◽  
Author(s):  
Yoo-Jin Park ◽  
Maria Agustina Battistone ◽  
Bongki Kim ◽  
Sylvie Breton

1983 ◽  
Vol 23 (2A) ◽  
pp. 175-182 ◽  
Author(s):  
Marcelle-Anne FAIN-MAUREL ◽  
J. P. DADOUNE ◽  
Françoise JAUZEIN-LEAU

Author(s):  
Mark H. Ellisman ◽  
Bridget Carragher ◽  
MaryAnn Martone

There are several types of intracellular membrane systems now known to be present in neurons. Much can be learned about the macromolecular composition and three dimensional distribution of many of these systems using the laser-scanning confocal microscope. However, detailed study of the morphology of these structures requires electron microscopy since most of the components of these intracellular systems are beyond the resolving power of the light microscope. Progress in selected research projects will be presented to provide examples for how new structural techniques are being used to study the internal membrane systems of neurons. Examples of membrane systems of neuronal cell bodies, and dendritic processes will be considered.


2021 ◽  
Vol 7 (1) ◽  
Author(s):  
Jianwu Shi ◽  
Kin Lam Fok ◽  
Pengyuan Dai ◽  
Feng Qiao ◽  
Mengya Zhang ◽  
...  

AbstractSpermatozoa acquire their fertilizing ability and forward motility during epididymal transit, suggesting the importance of the epididymis. Although the cell atlas of the epididymis was reported recently, the heterogeneity of the cells and the gene expression profile in the epididymal tube are still largely unknown. Considering single-cell RNA sequencing results, we thoroughly studied the cell composition, spatio-temporal differences in differentially expressed genes (DEGs) in epididymal segments and mitochondria throughout the epididymis with sufficient cell numbers. In total, 40,623 cells were detected and further clustered into 8 identified cell populations. Focused analyses revealed the subpopulations of principal cells, basal cells, clear/narrow cells, and halo/T cells. Notably, two subtypes of principal cells, the Prc7 and Prc8 subpopulations were enriched as stereocilia-like cells according to GO analysis. Further analysis demonstrated the spatially specific pattern of the DEGs in each cell cluster. Unexpectedly, the abundance of mitochondria and mitochondrial transcription (MT) was found to be higher in the corpus and cauda epididymis than in the caput epididymis by scRNA-seq, immunostaining, and qPCR validation. In addition, the spatio-temporal profile of the DEGs from the P42 and P56 epididymis, including transiting spermatozoa, was depicted. Overall, our study presented the single-cell transcriptome atlas of the mouse epididymis and revealed the novel distribution pattern of mitochondria and key genes that may be linked to sperm functionalities in the first wave and subsequent wave of sperm, providing a roadmap to be emulated in efforts to achieve sperm maturation regulation in the epididymis.


1966 ◽  
Vol 137 (2 Biological Me) ◽  
pp. 1038-1040 ◽  
Author(s):  
R. J. Podolsky ◽  
L. L. Costantin

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