Literature DB >> 2605373

Identification of the 16 degrees C compartment of the endoplasmic reticulum in rat liver and cultured hamster kidney cells.

D J Morré1, N Minnifield, M Paulik.   

Abstract

In many systems transfer between the endoplasmic reticulum and the Golgi apparatus is blocked at temperatures below 16 degrees C. In virus-infected cells in culture, a special membrane compartment is seen to accumulate. Our studies with rat liver show a similar response to temperature both in situ with slices and in vitro with isolated transitional endoplasmic reticulum fractions. With isolated transitional endoplasmic reticulum fractions, when incubated in the presence of nucleoside triphosphate and a cytosol fraction, temperature dependent formation of vesicles occurred with a Q10 of approximately 2 but was apparent only at temperatures greater than 12 degrees C. A similar response was seen in situ at 12 degrees C and 16 degrees C where fusion of transition vesicles with cis Golgi apparatus, but not their formation, was blocked and transition vesicles accumulated in large numbers. At 18 degrees C and below and especially at 8 degrees C and 12 degrees C, the cells responded by accumulating smooth tubular transitional membranes near the cis Golgi apparatus face. With cells and tissue slices at 20 degrees C neither transition vesicles nor the smooth tubular elements accumulated. Those transition vesicles which formed at 37 degrees C were of a greater diameter than those formed at 4 degrees C both in situ and in vitro. The findings show parallel responses between the temperature dependency of transition vesicle formation in vitro and in situ and suggest that a subpopulation of the transitional endoplasmic reticulum may be morphologically and functionally homologous to the 16 degrees C compartment observed in virally-infected cell lines grown at low temperatures.

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Year:  1989        PMID: 2605373      PMCID: PMC7161763          DOI: 10.1111/j.1768-322x.1989.tb03009.x

Source DB:  PubMed          Journal:  Biol Cell        ISSN: 0248-4900            Impact factor:   4.458


  19 in total

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Authors:  J Saraste; G E Palade; M G Farquhar
Journal:  Proc Natl Acad Sci U S A       Date:  1986-09       Impact factor: 11.205

2.  The effects of low temperatures on intracellular transport of newly synthesized albumin and haptoglobin in rat hepatocytes.

Authors:  E Fries; I Lindström
Journal:  Biochem J       Date:  1986-07-01       Impact factor: 3.857

3.  Inhibition of fast axonal transport of [3H]protein by cobalt ions.

Authors:  R Hammerschlag; A Y Chiu; A R Dravid
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4.  Pre- and post-Golgi vacuoles operate in the transport of Semliki Forest virus membrane glycoproteins to the cell surface.

Authors:  J Saraste; E Kuismanen
Journal:  Cell       Date:  1984-09       Impact factor: 41.582

5.  Interferon production by inactivated Newcastle disease virus in cell cultures and in mice.

Authors:  J S Youngner; A W Scott; J V Hallum; W R Stinebring
Journal:  J Bacteriol       Date:  1966-10       Impact factor: 3.490

6.  Temperature and energy dependence of secretory protein transport in the exocrine pancreas.

Authors:  A M Tartakoff
Journal:  EMBO J       Date:  1986-07       Impact factor: 11.598

7.  Temperature dependence of mast cell histamine secretion.

Authors:  D Lagunoff; H Wan
Journal:  J Cell Biol       Date:  1974-06       Impact factor: 10.539

8.  Improvements in epoxy resin embedding methods.

Authors:  J H LUFT
Journal:  J Biophys Biochem Cytol       Date:  1961-02

9.  Exit of newly synthesized membrane proteins from the trans cisterna of the Golgi complex to the plasma membrane.

Authors:  G Griffiths; S Pfeiffer; K Simons; K Matlin
Journal:  J Cell Biol       Date:  1985-09       Impact factor: 10.539

10.  Tunicamycin resistant glycosylation of coronavirus glycoprotein: demonstration of a novel type of viral glycoprotein.

Authors:  K V Holmes; E W Doller; L S Sturman
Journal:  Virology       Date:  1981-12       Impact factor: 3.616

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  5 in total

1.  Temperature- and acceptor-specificity of cell-free vesicular transfer from transitional endoplasmic reticulum to the cis Golgi apparatus.

Authors:  S Dunkle; T Reust; D D Nowack; L Waits; M Paulik; D M Morre; D J Morre
Journal:  Biochem J       Date:  1992-12-15       Impact factor: 3.857

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Authors:  D J Morré; G Selldén; C Sundqvist; A S Sandelius
Journal:  Plant Physiol       Date:  1991-12       Impact factor: 8.340

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Authors:  J K Hoober; R A White; D B Marks; J L Gabriel
Journal:  Photosynth Res       Date:  1994-01       Impact factor: 3.573

4.  The isolated ER-Golgi intermediate compartment exhibits properties that are different from ER and cis-Golgi.

Authors:  A Schweizer; K Matter; C M Ketcham; H P Hauri
Journal:  J Cell Biol       Date:  1991-04       Impact factor: 10.539

5.  A brief history of thylakoid biogenesis.

Authors:  Annabel Mechela; Serena Schwenkert; Jürgen Soll
Journal:  Open Biol       Date:  2019-01-31       Impact factor: 6.411

  5 in total

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