Literature DB >> 3744900

Effects of leupeptin on endocytosis and membrane recycling in rat visceral yolk-sac endoderm.

A Miki, P Kugler.   

Abstract

The effect of exposure to leupeptin (25 micrograms/ml for 24 h) on the endocytotic activity and the membrane flow of apical cell membranes was studied in endodermal cells of cultured rat visceral yolk sacs by applying a double-labelling method using concanavalin-A ferritin (Con-A Fer) and horseradish peroxidase (HRP). Control and leupeptin-treated yolk sacs were labelled with Con-A Fer at 4 degrees C and then incubated with HRP for 5, 15 or 60 min at 37 degrees C. In controls, HRP reaction product was detected after 5 min in many of the apical vacuoles as well as a few lysosomes; after 15 min, reaction product was observed in all apical vacuoles and in lysosomes of various sizes. These HRP-positive structures usually contained a variable amount of membrane-bound Fer. After 60 min, all apical vacuoles and almost all lysosomes exhibited HRP reactions, but only some of these structures contained Fer particles. At this time, many apical canaliculi (which are involved in membrane recycling) exhibited positive HRP reactions and sometimes also contained Fer particles. In leupeptin-treated cells, HRP reaction product and variable amounts of membrane-bound Fer particles were found in apical vacuoles after 5 min; after 15 min, both labels were also observed in some small lysosomes, and after 60 min, they were found in all apical vacuoles as well as some small and middle-sized lysosomes. Significantly fewer labelled apical vacuoles, lysosomes and apical canaliculi were present after leupeptin treatment than in controls at corresponding times. At all times examined, the giant lysosomes found in leupeptin-treated cells did not exhibit any labeling.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1986        PMID: 3744900     DOI: 10.1007/bf00491765

Source DB:  PubMed          Journal:  Histochemistry        ISSN: 0301-5564


  30 in total

1.  Inhibition of protein degradation in isolated rat hepatocytes.

Authors:  M F Hopgood; M G Clark; F J Ballard
Journal:  Biochem J       Date:  1977-05-15       Impact factor: 3.857

2.  [Effect of leupeptin on protein uptake and the degradation of the visceral yolk sac epithelium of the rat].

Authors:  P Kugler; T Beckenbauer
Journal:  Z Mikrosk Anat Forsch       Date:  1987

3.  An ultrastructural comparison of the uptake and transport of horseradish peroxidase by the rat visceral yolk-sac placenta during mid- and late gestation.

Authors:  W Seibel
Journal:  Am J Anat       Date:  1974-06

4.  Protein absorption and transport by the guinea pig visceral yolk sac placenta.

Authors:  B F King; A C Enders
Journal:  Am J Anat       Date:  1970-11

5.  Intracellular degradation of 125I-labelled asialo-glycoproteins in rat hepatocytes: effect of leupeptin on subcellular distribution of asialo-fetuin.

Authors:  T Berg; T Ose; L Ose; H Tolleshaug
Journal:  Int J Biochem       Date:  1981

6.  The cellular specificity of lectin binding in the kidney. I. A light microscopical study in the rat.

Authors:  M Le Hir; U C Dubach
Journal:  Histochemistry       Date:  1982

7.  The effect of cathepsin inhibitor on rat embryos grown in vitro.

Authors:  F Beck; A Lowy
Journal:  J Embryol Exp Morphol       Date:  1982-10

8.  Cathepsin L. A new proteinase from rat-liver lysosomes.

Authors:  H Kirschke; J Langner; B Wiederanders; S Ansorge; P Bohley
Journal:  Eur J Biochem       Date:  1977-04-01

9.  Quantitation of rat embryonic development in vitro: a morphological scoring system.

Authors:  N A Brown; S Fabro
Journal:  Teratology       Date:  1981-08

10.  Hydrolase secretion is a consequence of membrane recycling.

Authors:  T C Hohman; B Bowers
Journal:  J Cell Biol       Date:  1984-01       Impact factor: 10.539

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  2 in total

1.  Reabsorption of fluorescein-isothiocyanate-labelled-ovalbumin in the kidney of normal and castrated male and female rats.

Authors:  L Sievers; P Kugler
Journal:  Histochemistry       Date:  1986

Review 2.  Vacuoles in mammals: a subcellular structure indispensable for early embryogenesis.

Authors:  Yoh Wada
Journal:  Bioarchitecture       Date:  2013 Jan-Feb
  2 in total

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