scholarly journals Radioautographic Analysis of the Secretory Pathway for Glycoproteins in Principal Cells of the Mouse Epididymis Exposed to [3H] Fucose

1985 ◽  
Vol 32 (2) ◽  
pp. 377-389 ◽  
Author(s):  
Charles J. Flickinger
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

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.


Endocrinology ◽  
2007 ◽  
Vol 148 (7) ◽  
pp. 3196-3204 ◽  
Author(s):  
Dwi Ari Pujianto ◽  
Anastasios E. Damdimopoulos ◽  
Petra Sipilä ◽  
Jenni Jalkanen ◽  
Ilpo Huhtaniemi ◽  
...  

B-cell lymphoma 2 (BCL2) family kin (BFK) is a recently identified novel protein that is similar to proteins of the BCL2 family. In the present study, we discovered that the mouse Bfk transcript is expressed at the highest level in the epididymis. Two transcripts of 0.9 and 2.6 kb in size were identified, with alternative exon 4 structures, resulting in a difference in the last three to five amino acids of the variants. However, the 0.9-kb transcript was found to be the predominant form in the epididymis and mammary gland, another tissue with strong Bfk expression. Epididymal Bfk expression was regulated both by androgens and other testicular factors. It is thus one of the few initial-segment enriched genes under androgen control, the majority of them being regulated by other testicular factors. BFK protein was expressed specifically in the principal cells of the epididymis. Its nuclear localization was evident in the initial segment and caput epididymis and in the epithelium of pregnant female mammary gland. The expression of BFK-enhanced green fluorescent protein recombinant protein in epididymal cells further confirmed the predominant nuclear localization of BFK with nucleo-cytoplasmic shuttling. Overexpressing BFK in epididymal cells did not induce apoptosis. However, enhanced caspase 3 activation was observed in the presence of BFK upon staurosporine-induced apoptosis. This suggests that BFK may have a proapoptotic role only after the process has been initiated by other mechanisms. Being exceptionally highly expressed in the initial segment, Bfk is suggested to have a role in the differentiation of this segment of the epididymis.


2005 ◽  
Vol 173 (4S) ◽  
pp. 301-301
Author(s):  
Chung Kuang Su ◽  
Jonathan N. Rubenstein ◽  
Affonso H.L.A. Camargo ◽  
Stephen L. Gluck ◽  
Marshall L. Stoller

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