## Abstract Stop‐flow techniques were used to determine how temperature affected the axonal transport of dopamine‐β‐hydroxylase (DBH) activity in rabbit sciatic nerves __in vitro.__ These nerves were cooled locally to 2°C for 1.5 hr, which caused a sharp peak of DBH activity to accumulate above the
Rapid axonal transport of phosphatidylinositol in the rabbit optic pathway
✍ Scribed by M. Alberghina; M. Viola; Prof. A. M. Giuffrida
- Publisher
- John Wiley and Sons
- Year
- 1981
- Tongue
- English
- Weight
- 516 KB
- Volume
- 6
- Category
- Article
- ISSN
- 0360-4012
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
At different time intervals (4 hr up to 24 days) after intravitreal injection of myo‐(2‐^3^H)‐inositol, the specific activity (sp act) of phosphatidylinositol (PtdIns) and water‐soluble compounds extracted from the retina, optic nerve (ON), optic tract (OT), lateral geniculate body (LGB), and superior colliculus (SC) was measured. Furthermore, 2 days after biocular injection of the labeled precursor, the specific activity of PtdIns and other major phospholipids in the various subcellular fractions (myelin, axolemma, synaptosomes, mitochondria, and microsomes) purified from ON + OT, from LGB, and from SC was evaluated. In the ON and OT, the phospholipids were labeled 8 hr after the precursor injection; in the LGB and SC after 8–12 hr. In all the optic components examined, the lipid specific activity reached a maximum at day 6 and decreased slowly until day 24 after injection. In the ON + OT, the specific activity of PtdIns, isolated from various subcellular fractions, decreased as follows: myelin > axolemma; in the LGB and SC as follows: microsomes > synaptosomes > myelin > mitochondria. The radioactivity present in the retina and in the optic pathway was exclusively localized in the PtdIns during the whole time interval studied. Ten days after the precursor injection, a high portion of the radioactivity transported was detected in the water‐soluble pool, separated from the ON and OT, whereas no significant counts in the corresponding LGB and SC pool were found. The kinetics of PtdIns labeling, observed in the different optic components, indicated a rapid axonal transport of the phospholipid; besides, the presence of labeled PtdIns in the purified myelin suggested a transaxonal migration of the phospholipid and its free precursor.
📜 SIMILAR VOLUMES
the sciatic nerve. Most synaptic vesicle proteins were colo-ABSTRACT: The optic nerve, as a part of the cencalized in the axons proximal to the crush. A differential tral nervous system (CNS), has been used to study axonal distribution of synaptobrevin I and II, however, was obtransport for decades.
Post-Golgi trafficking of the major fast axonally transported (FT) proteins was investigated in the rat optic pathway. Following intra-ocular injection of 35 Smethionine, radiolabeled FT proteins in the optic tract (OT) and superior colliculus (SC) were analyzed by twodimensional polyacrylamide gel
## Abstract Phosphatidylinositol 3‐kinase (PI3‐kinase) and phosphatidylinositol 4‐kinase (PI4‐kinase) enzymes are an important family of signaling molecules that have been implicated in the regulation of intracellular vesicle trafficking. It has previously been shown that PI3‐kinase and PI4‐kinase
## Abstract HRP was injected in the flocculonodular lobe and the paraflocculus in the rabbit to determine the areas of the inferior olive which project onto these cerebellar regions. Following injections in the flocculus labeled cells occurred in the dorsal cap and the rostralmost tip of the medial