Seminal Plasma Biochemistry II Seminal Plasma and Spermatozoal Cytidine Monophosphate-Sialic Acid Synthetase and Sialyltransferase Activities

Andrologia ◽  
2009 ◽  
Vol 13 (3) ◽  
pp. 215-224 ◽  
Author(s):  
B. DAUNTER ◽  
J. NEWLANDS
1963 ◽  
Vol 40 (4) ◽  
pp. 587-594
Author(s):  
H. BARNES

1. The seminal plasma of Balanus balanus has been analysed for a number of organic substances including total nitrogen, protein, urea, protein-bound hexose, hexosamine, fucose, ‘sialic acid’, glycogen, and RNA. The material was separated into soluble and insoluble fractions by precipitation with ethanol. 2. A large part of the ethanol-soluble material is inorganic salts and glycine; it contains a small quantity of protein-like material which on hydrolysis yields largely glycine and glutamic acid. 3. The alcohol-precipitated material contains protein, protein-bound hexose, hexosamine, lipids, and RNA. Glycogen, fucose, and ‘sialic acid’ are absent. 4. It is suggested that the plasma contains glycoproteins of a mucoid nature: the absence of both fucose and ‘sialic acid’ suggests that the mucoid may be of a relatively simple character. 5. Attention is drawn to the similarity of this seminal plasma, which is produced in the absence of accessory male organs, to that of higher animals.


1983 ◽  
Vol 10 (1) ◽  
pp. 45-46 ◽  
Author(s):  
H. Levinsky ◽  
R. Singer ◽  
M. Barnet ◽  
M. Sagiv ◽  
D. Allalouf

2014 ◽  
Vol 81 (3) ◽  
pp. 373-380 ◽  
Author(s):  
Mehmet Bozkurt Ataman ◽  
Hasan Hüseyin Dönmez ◽  
Nurcan Dönmez ◽  
Emrah Sur ◽  
Mustafa Numan Bucak ◽  
...  

2021 ◽  
Vol 8 ◽  
Author(s):  
Estrella Lopez-Gordo ◽  
Alejandro Orlowski ◽  
Arthur Wang ◽  
Alan Weinberg ◽  
Susmita Sahoo ◽  
...  

Adeno-associated virus (AAV) vectors are promising candidates for gene therapy. However, a number of recent preclinical large animal studies failed to translate into the clinic. This illustrates the formidable challenge of choosing the animal models that promise the best chance of a successful translation into the clinic. Several of the most common AAV serotypes use sialic acid (SIA) as their primary receptor. However, in contrast to most mammals, humans lack the enzyme CMAH, which hydroxylates cytidine monophosphate-N-acetylneuraminic acid (CMP-Neu5Ac) into cytidine monophosphate-N-glycolylneuraminic acid (CMP-Neu5Gc). As a result, human glycans only contain Neu5Ac and not Neu5Gc. Here, we investigate the tropism of AAV1, 5, 6 and 9 in wild-type C57BL/6J (WT) and CMAH knock-out (CMAH−/−) mice. All N-linked SIA-binding serotypes (AAV1, 5 and 6) showed significantly lower transduction of the heart in CMAH−/− when compared to WT mice (5–5.8-fold) and, strikingly, skeletal muscle transduction by AAV5 was almost 30-fold higher in CMAH−/− compared to WT mice. Importantly, the AAV tropism or distribution of expression among different organs was also affected. For AAV1, AAV5 and AAV6, expression in the heart compared to the liver was 4.6–8-fold higher in WT than in CMAH−/− mice, and for AAV5 the expression in the heart compared to the skeletal muscle was 57.3-fold higher in WT than in CMAH−/− mice. These data thus strongly suggest that the relative abundance of Neu5Ac and Neu5Gc plays a role in AAV tropism, and that results obtained in commonly used animal models might not translate into the clinic.


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