scholarly journals A purkinje cell-specific protein (spot 35 protein) showing wide distribution in the endocrine system of some mammals. An immunohistochemical study.

1986 ◽  
Vol 19 (5) ◽  
pp. 545-553 ◽  
Author(s):  
ISAO HOZUMI ◽  
TOSHIHIKO IWANAGA ◽  
TSUNEO FUJITA ◽  
TOHRU YAMAKUNI ◽  
YASUO TAKAHASHI
2017 ◽  
Vol 81 ◽  
pp. 87-96 ◽  
Author(s):  
Samah Kandeel ◽  
Naema Mahmoud Elhosary ◽  
Mona Mohamed Abo El-Noor ◽  
Mohamed Balaha

Parasitology ◽  
1984 ◽  
Vol 89 (2) ◽  
pp. 253-262 ◽  
Author(s):  
Hilary Hurd ◽  
C. Arme

SummaryThe effects of metacestodes ofHymenolepis diminutaon haemolymph proteins ofTenebrio molitorare restricted to female hosts. In beetles aged 15 days post-emergence, and harbouring 12-day-old metacestodes, haemolymph concentration is 46·7% higher than in non-infected animals and similar effects are found in longer standing infections. Electrophoresis of haemolymph revealed the presence of 13 bands. Densitometric analysis showed that only band 2/3 was significantly elevated in infected hosts although band 7/8 also showed an increase. These bands were also present in egg homogenates and are thought to be vitellogenins. It is therefore proposed that the excess protein found in infected beetles is a female-specific protein resulting from an interaction between the parasite and the host endocrine system.


1993 ◽  
Vol 26 (5) ◽  
pp. 405-414 ◽  
Author(s):  
HIROYUKI OHTSUKA ◽  
TOSHIHIKO IWANAGA ◽  
MASAYUKI A. FUJINO ◽  
TSUNEO FUJITA

2021 ◽  
Vol 116 (1) ◽  
Author(s):  
Vladimir Bogdanov ◽  
Andrew M. Soltisz ◽  
Nicolae Moise ◽  
Galina Sakuta ◽  
Benjamin Hernandez Orengo ◽  
...  

AbstractIt is widely assumed that synthesis of membrane proteins, particularly in the heart, follows the classical secretory pathway with mRNA translation occurring in perinuclear regions followed by protein trafficking to sites of deployment. However, this view is based on studies conducted in less-specialized cells, and has not been experimentally addressed in cardiac myocytes. Therefore, we undertook direct experimental investigation of protein synthesis in cardiac tissue and isolated myocytes using single-molecule visualization techniques and a novel proximity-ligated in situ hybridization approach for visualizing ribosome-associated mRNA molecules for a specific protein species, indicative of translation sites. We identify here, for the first time, that the molecular machinery for membrane protein synthesis occurs throughout the cardiac myocyte, and enables distributed synthesis of membrane proteins within sub-cellular niches where the synthesized protein functions using local mRNA pools trafficked, in part, by microtubules. We also observed cell-wide distribution of membrane protein mRNA in myocardial tissue from both non-failing and hypertrophied (failing) human hearts, demonstrating an evolutionarily conserved distributed mechanism from mouse to human. Our results identify previously unanticipated aspects of local control of cardiac myocyte biology and highlight local protein synthesis in cardiac myocytes as an important potential determinant of the heart’s biology in health and disease.


1989 ◽  
Vol 76 (2) ◽  
pp. 171-191 ◽  
Author(s):  
R. Perez-Tomas ◽  
J. Ballesta ◽  
L.M. Pastor ◽  
J.F. Madrid ◽  
J.M. Polak

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