scholarly journals THE EFFECTS OF SECRETAGOGUES ON THE INCORPORATION OF [2-3H]MYOINOSITOL INTO LIPID IN CYTOLOGICAL FRACTIONS IN THE PANCREAS OF THE GUINEA PIG IN VIVO

1973 ◽  
Vol 56 (3) ◽  
pp. 736-745 ◽  
Author(s):  
Dorothy Gerber ◽  
Margaret Davies ◽  
Lowell E. Hokin
Keyword(s):  
Endoplasmic Reticulum ◽  
Single Injection ◽  
Enzyme Secretion ◽  
Amylase Level ◽  
Membrane Flow ◽  
Secretory Cycle ◽  
Microsome Fraction ◽  
Stimulation Of ◽  
Cholinergic Drug

Stimulation of enzyme secretion in the pancreas on injection of a single dose of the cholinergic drug, pilocarpine, was associated with an increased incorporation of [2-3H]myoinositol into a lipid, which was previously characterized as phosphatidylinositol. Stimulation of enzyme secretion by hourly injection of the pancreozymin congener, caerulein, led to more increased phosphatidylinositol synthesis than with a single injection of pilocarpine. The amylase level of the pancreas remained at a low level as long as caerulein was injected, indicating continued stimulation of enzyme secretion even though increased phosphatidylinositol synthesis ceased after 6 h. Feeding gave the same stimulation of phosphatidylinositol synthesis as caerulein. The major synthesis of phosphatidylinositol in controls and the stimulation of phosphatidylinositol synthesis by pilocarpine was entirely confined to the microsome fraction throughout the experiments (up to 18 h). This shows that there is no flow of microsomal membrane (smooth- or rough-surfaced endoplasmic reticulum) to other membranous structures throughout the secretory cycle and beyond. It is concluded that the stimulation of phosphatidylinositol synthesis by pancreatic secretagogues is confined to microsomal elements and does not play any role in membrane flow.

scholarly journals The formation, distribution and function of ribosomes and microsomal membranes during induced amphibian metamorphosis

1967 ◽  
Vol 105 (2) ◽  
pp. 783-801 ◽  
Author(s):  
J. R. Tata
Keyword(s):  
Endoplasmic Reticulum ◽  
Ribosomal Proteins ◽  
Specific Activity ◽  
Tail Length ◽  
Similar Response ◽  
Carbamoyl Phosphate ◽  
Microsomal Membranes ◽  
Stimulation Of ◽  
Induction Of Metamorphosis

1. A lag period of about 4 days preceded the onset of metamorphosis precociously induced by tri-iodothyronine in tadpoles of the giant American bullfrog (Rana catesbeiana). It was established by the accelerated synthesis or induction of carbamoyl phosphate synthetase and cytochrome oxidase in the liver, serum albumin and adult haemoglobin in the blood, acid phosphatase in the tail, and the increase in the hindleg/tail length ratio. 2. A 4- to 6-fold stimulation, 2 days after the induction of metamorphosis, of the rate of synthesis of rapidly labelled nuclear RNA in liver cells was followed by an increasing amount of RNA appearing in the cytoplasm. Most of the newly formed RNA on induction of metamorphosis was of the ribosomal type. An accelerated turnover at early stages of development preceded a net accumulation of RNA in the cytoplasm, with no change in the amount of DNA per liver. 3. Most hepatic ribosomes of the pre-metamorphic tadpoles were present as 78s monomers and 100s dimers; metamorphosis caused a shift towards larger polysomal aggregates with newly formed ribosomes that were relatively more tightly bound to membranes of the endoplasmic reticulum. 4. The appearance of new polyribosomes in the cytoplasm on induction of metamorphosis was co-ordinated in time with a stimulation of synthesis of phospholipids of the smooth and rough endoplasmic reticulum, followed by a gradual shift in preponderance from the smooth to the rough type of microsomal membranes. 5. Electron- and optical-microscopic examination of intact hepatocytes revealed a striking change in the distribution and nature of ribosomes and microsomal membranes during metamorphosis. 6. Ribosomes prepared from non-metamorphosing and metamorphosing animals were identical in their sedimentation coefficients and in the structural ribosomal proteins. The base composition and sedimentation coefficients of ribosomal RNA were also identical. Induction of metamorphosis also did not alter the incorporation of 32P into the different phospholipid constituents of microsomal membranes. 7. Nascent 14C-labelled protein with the highest specific activity was recovered in the ‘heavy’ rough membrane fraction of microsomes, whereas little 14C was associated with ‘free’ polysomes. Protein synthesis in vivo was most markedly stimulated during metamorphosis in the tightly membrane-bound ribosomal fraction after the appearance of new ribosomes. 8. The rate of synthesis of macromolecules in vivo could not be followed beyond 7–8 days after induction because of variable shifts in precursor pools due to regression of larval tissues. 9. The stimulation of RNA and ribosome formation was specifically associated with the process of metamorphosis since no similar response to thyroid hormones occurred in those species (Axolotl and Necturus) in which the hormones failed to induce metamorphosis.

scholarly journals THE SECRETORY PATHWAYS OF RAT SERUM GLYCOPROTEINS AND ALBUMIN

1972 ◽  
Vol 52 (2) ◽  
pp. 231-245 ◽  
Author(s):  
Colvin M. Redman ◽  
M. George Cherian
Keyword(s):  
Endoplasmic Reticulum ◽  
Membrane Protein ◽  
Rough Endoplasmic Reticulum ◽  
Serum Proteins ◽  
Rat Serum ◽  
Secretory Pathways ◽  
Specific Antisera ◽  
Microsome Fraction

These studies compare the secretory pathways of newly formed rat serum glycoproteins and albumin by studying their submicrosomal localization at early times after the beginning of their synthesis and also by determining the submicrosomal site of incorporation of N-acetylglucosamine, mannose, galactose, and leucine into protein. N-acetylglucosamine, mannose, and galactose were only incorporated in vitro into proteins from membrane-attached polysomes and not into proteins from free polysomes. Mannose incorporation occurred in the rough endoplasmic reticulum, was stimulated by puromycin but not by cycloheximide, and 90% of the mannose-labeled protein was bound to the membranes. Galactose incorporation, by contrast, occurred in the smooth microsome fraction and 89% of the radioactive protein was in the cisternae. Albumin was mostly recovered (98%) in the cisternae, with negligible amounts in the membranes. To determine whether the radio-active sugars were being incorporated into serum proteins or into membrane protein, the solubilized in vivo-labeled proteins were treated with specific antisera to rat serum proteins or to albumin. Immunoelectrophoresis of the 14C-labeled leucine membrane and cisternal proteins showed that the membranes contained radioactive serum glycoprotein but no albumin, while the cisternal fraction contained all of the radioactive albumin and some glycoproteins. The results indicate that newly formed serum glycoproteins remain attached to the membranes of the rough endoplasmic reticulum after they are released from the membrane-attached polysomes, while albumin passes directly into the cisternae.

scholarly journals IN VITRO STIMULATION OF ENZYME SECRETION AND THE SYNTHESIS OF MICROSOMAL MEMBRANES IN THE PANCREAS OF THE GUINEA PIG

1971 ◽  
Vol 51 (2) ◽  
pp. 396-404 ◽  
Author(s):  
Jacopo Meldolesi ◽  
Dario Cova
Keyword(s):  
Guinea Pig ◽  
High Ionic Strength ◽  
Enzyme Secretion ◽  
Secretory Cells ◽  
Secretory Cycle ◽  
Golgi Membranes ◽  
Granule Membrane ◽  
Microsomal Membranes ◽  
Stimulation Of

Several mechanisms have been suggested to explain how secretory cells remove from the plasmalemma the excess membrane resulting from the insertion of granule membrane during exocytosis: intact patches of membrane may be internalized and then reutilized within the cell; alternatively these membranes may be either disassembled to subunits or degraded. In the latter case new membranes should be synthetized at other sites of the cell, probably in the rough-surfaced endoplasmic reticulum (RER) and the Golgi complex. In the present research, membrane subfractions were obtained from rough microsomes (derived from fragmented and resealed RER cisternae) and from smooth microsomes (primarily contributed by Golgi stacks and vesicles) of the guinea pig pancreas by incubation at 4°C for 4 hr in 0.0005 M puromycin at high ionic strength followed by mild (pH 7.8) alkaline extraction with 0.2 M NaHCO3. Such treatments release the majority of nonmembrane components of both microsomal fractions (i.e., contained secretory enzymes, ribosomes, and absorbed proteins of the cell sap) and allow the membranes to be recovered by centrifugation. The effect of in vitro stimulation of enzyme secretion (brought about in pancreas slices by 0.0001 M carbamoyl choline) on the rate of synthesis of the phospholipid (PLP) and protein of these membranes was then investigated. In agreement with previous data, we observed that in stimulated slices the synthesis of microsomal PLP was greatly increased. In contrast, the synthesis of microsomal membrane proteins was unchanged. These results suggest that exocytosis is not coupled with an increased rate of synthesis of complete ER and Golgi membranes and are, therefore, consistent with the view that excess plasma membrane is preserved and reutilized, either as discrete membrane patches or as membrane macromolecules, throughout the secretory cycle.

scholarly journals RADIOAUTOGRAPHIC LOCALIZATION OF THE INCREASED SYNTHESIS OF PHOSPHATIDYLINOSITOL IN RESPONSE TO PANCREOZYMIN OR ACETYLCHOLINE IN GUINEA PIG PANCREAS SLICES

1967 ◽  
Vol 33 (3) ◽  
pp. 521-530 ◽  
Author(s):  
Lowell E. Hokin ◽  
Dorothy Huebner
Keyword(s):  
Endoplasmic Reticulum ◽  
Guinea Pig ◽  
Acinar Cell ◽  
Protein Transport ◽  
Kinetic Studies ◽  
Pancreatic Acinar Cell ◽  
Enzyme Secretion ◽  
Golgi Membranes ◽  
Chloroform Methanol ◽  
Stimulation Of

A technique is described for measuring the incorporation of myo-inositol-2-3H into the lipid of various regions of the guinea pig pancreatic acinar cell by radioautography. Stimulation of enzyme secretion with either pancreozymin or acetylcholine was associated with increased graining in both the basophilic cytoplasm and the nonbasophilic cytoplasm. Kinetic studies suggested that the incorporation of myo-inositol-2-3H was stimulated independently in the two regions. Most of the increment in graining due to stimulation with pancreozymin or acetylcholine plus eserine was abolished if the tissue was extracted with 2:1 chloroform-methanol before radioautography. On chromatography of lipid extracts of pancreas, the only lipid showing a detectable increment in radioactivity on stimulation with pancreozymin was phosphatidylinositol. Thus, essentially all of the increment in graining is likely to be due to increased incorporation of tritium into phosphatidylinositol. These studies, coupled with earlier studies employing differential centrifugation, indicate that on stimulation of enzyme secretion there is increased synthesis of phosphatidylinositol in the rough-surfaced endoplasmic reticulum and in the smooth-surfaced Golgi membranes. The significance of these observations is discussed in connection with membrane circulation presumed to occur in the pancreatic acinar cell on stimulation of protein secretion. It is suggested that the increased synthesis of phosphatidylinositol may be concerned with the formation of new endoplasmic reticulum and possibly Golgi membrane to replace that which is presumably converted to membrane of the zymogen granules during intracellular protein transport.

DISSOCIATION OF THE CALORIGENIC ACTION OF THYROID HORMONES FROM THE DEIODINATION OF L-THYROXINE IN VIVO

1965 ◽  
Vol 48 (3) ◽  
pp. 506-512 ◽  
Author(s):  
M. Anbar ◽  
M. Inbar ◽  
J. R. Tata
Keyword(s):  
Thyroid Hormones ◽  
Metabolic Rate ◽  
Basal Metabolic Rate ◽  
Actinomycin D ◽  
Single Injection ◽  
Small Doses ◽  
Double Isotope ◽  
Stimulation Of

ABSTRACT The rate of deiodination of L-thyroxine was measured in vivo in normal and thyroidectomized rats by a technique of double isotope (125I and 131I) labelling. Small doses of Actinomycin D administered at the same time as 3,5,3′-triiodo-L-thyronine or L-thyroxine almost completely abolished the stimulatory effect of the hormones on basal metabolic rate (B. M. R.) but slightly elevated the rate of deiodination of L-thyroxine. When studied sequentially, the stimulation of B. M. R. preceded the increase in rate of deiodination of the hormone following a single injection of triiodothyronine to thyroidectomized rats. These results suggest that the rate of deiodination is not directly associated with the action of thyroid hormones.

Intracellular Ca2+ in pancreatic acinar cells: Regulation and role in stimulation of enzyme secretion

1987 ◽  
Vol 7 (4) ◽  
pp. 333-344 ◽  
Author(s):  
Robert L. Dormer ◽  
Graham R. Brown ◽  
Claire Doughney ◽  
Margaret A. McPherson
Keyword(s):  
Endoplasmic Reticulum ◽  
Pancreatic Enzyme ◽  
Acinar Cells ◽  
Enzyme Secretion ◽  
Pancreatic Acinar Cells ◽  
Current Evidence ◽  
Primary Role ◽  
Direct Demonstration ◽  
Pancreatic Enzyme Secretion ◽  
Stimulation Of

Evidence for a primary role for intracellular Ca2+ in the stimulation of pancreatic enzyme secretion is reviewed. Measurements of cytoplasmic free Ca2+ concentration have allowed direct demonstration of its importance in triggering enzyme secretion and defined the concentration range over which membrane Ca2+ pumps must work to regulate intracellular Ca2+. Current evidence suggests a key role for the Ca2+ Mg-ATPase of rough endoplasmic reticulum in regulating intracellular Ca2+ and accumulating a Ca2+ store which is released by the action of inositol-l,4,5 trisphosphate following stimulation of secretion.

scholarly journals Phospholipide Turnover in Microsomal Membranes of the Pancreas during Enzyme Secretion

1959 ◽  
Vol 6 (2) ◽  
pp. 207-214 ◽  
Author(s):  
Colvin M. Redman ◽  
Lowell E. Hokin
Keyword(s):  
Soluble Fraction ◽  
Cellular Component ◽  
Enzyme Secretion ◽  
Zymogen Granules ◽  
Membranous Structure ◽  
Microsomal Membranes ◽  
Microsome Fraction ◽  
The Individual ◽  
Soluble Components ◽  
Stimulation Of

After incubation of pigeon pancreas slices with P32 and isolation of various fractions by differential centrifugation the deoxycholate extract of the microsome fraction was found to account for over half of the phospholipide P and over half of the P32 incorporated into the phospholipides. The remaining phospholipide P and P32 were fairly evenly distributed in the nuclei, zymogen granules, mitochondria, microsomal ribonucleoprotein particles, and the soluble fraction. When enzyme secretion was stimulated with acetylcholine about two-thirds of the increment in radioactivity in the total phospholipides was found in deoxycholate soluble components of the microsome fraction. The remainder of the increment was distributed in the other fractions. This indicates that the cellular component in which the increase in phospholipide turnover occurs on stimulation of secretion is a membranous structure. Evidence is presented which indicates that the increment in radioactivity in the non-microsomal fractions on stimulation of secretion is due to contamination of these fractions with fragments of the stimulated membranous structure. The distribution of P32 radioactivity in each of the chromatographically separated phospholipides in the various fractions from unstimulated tissue paralleled the distribution of radioactivity in the total phospholipide fraction, indicating that individual phospholipides are not concentrated in different fractions but are associated together in the membranous structures of the microsome fraction. The major proportion of the stimulation of the turnover of the individual phospholipides also occurred in the microsome fraction. The distribution of radioactivity from glycerol-1-C14 in the total phospholipides and in the individual phospholipides in the various fractions was similar to the distribution of P32. In the microsome fraction acetylcholine stimulated the incorporation of glycerol-1-C14 in each phospholipide which showed a stimulation of P32 incorporation. The significance of the turnover of phosphatides in microsomal membranes in relation to the mechanism of secretion is discussed.

scholarly journals Turnover of metallothioneins in rat liver

1978 ◽  
Vol 174 (1) ◽  
pp. 327-338 ◽  
Author(s):  
R D Andersen ◽  
W P Winter ◽  
J J Maher ◽  
I A Bernstein
Keyword(s):  
Radioactive Isotope ◽  
Single Injection ◽  
Thiol Group ◽  
Control Value ◽  
Metal Treatment ◽  
Wet Weight ◽  
Cdcl2 Treatment ◽  
Stimulation Of ◽  
Rate Of Accumulation

Two electrophoretically distinguishable metallothioneins were isolated from the livers of Cd2+-treated rats and had thiol group/metal ratios of 3:1, a total metal content, in each of these proteins, of 3.6 atoms of Cd2+ + 2.4 atoms of Zn2+/molecule and 4.2 atoms of Cd2+ + 2.8 atoms of Zn2+/molecule and respective apoprotein mol.wts. of 5844 and 6251. Studies with 1 h pulse labels of [3H]cysteine, given after a single injection of ZnCl2 or CdCl2, showed that these metals stimulated radioactive isotope incorporation into the metallothioneins over the control value by 10- and 15-fold respectively. This stimulation was maximal at 4 h after a single CdCl2 injection and decreased to control values by 16 h, suggesting that either a translational event is responding to free intracellular Cd2+ or a short-lived mRNA is being produced or stabilized in response to the metal treatment. In rats chronically exposed to CdCl2, the metallothioneins increased to 0.2% of the liver wet weight from a control value of 2–4 mumol/kg of liver, with a maximum rate of accumulation of 2–3 mumol/h per kg of liver. The turnover of these proteins in control animals was 0.3–0.6 mumoles/h per kg of liver, measured by the rate of disappearance of 203Hg2+, which binds irreversibly to the metallothioneins. Pretreatment with CdCl2 completely stopped the rapid 203Hg turnover observed in untreated animals. Unlike CdCl2, treatment with ZnCl2 increased the concentration of metallothioneins to a new steady-state pool, 11 mumole/kg of liver, after 10 h. The increase in the zinc-thionein pool by exposure to ZnCl2 in vivo was determined to be primarily due to a stimulation of metallothionein biosynthesis.

Suitability of L-[35S]methionine for studying the biosynthesis of the polypeptides of mouse liver endoplasmic reticulum membrane fractions in vivo

1979 ◽  
Vol 57 (6) ◽  
pp. 625-638 ◽  
Author(s):  
Monique Behar-Bannelier ◽  
Rajendra N. Sharma ◽  
Robert K. Murray
Keyword(s):  
Endoplasmic Reticulum ◽  
Mouse Liver ◽  
Serum Proteins ◽  
Sodium Dodecyl ◽  
Endoplasmic Reticulum Membrane ◽  
Membrane Flow ◽  
Adult Mice ◽  
Coomassie Blue ◽  
Er Membrane

The use of L-[35S]methionine (500–700 Ci/mmol (1 Ci = 37 GBq)) for labelling the polypeptides of liver rough (R) and smooth (S) endoplasmic reticulum (ER) membrane fractions in vivo was studied. Adult mice were injected intraperitoneally with 400 μCi of the isotope and killed at various times (2 min to 24 h) thereafter. RER and SER fractions were prepared, stripped of ribosomes, and treated with Triton X-100 to remove intravesicular contents. Sufficient radioactivity was present in individual aliquots (75 μg protein) of the ER membrane fractions to permit their analysis by fluorography after separation by electrophoresis in polyacrylamide gels containing sodium dodecyl sulphate. By 3 min, although the majority of the labelled components were of intravesicular origin, some 12 membrane polypeptides were labelled in the RER fraction (including one corresponding in migration to cytochrome P-450); some 6 of these latter polypeptides were labelled to a lesser degree in the SER membrane fraction at this time. By 5 min, the patterns of radioactive polypeptides of the RER and SER fractions (including both membrane and intravesicular components) were identical. By 7 min, some 28 labelled membrane polypeptides were detectable in the total microsomal membrane. Analysis of the 24-h samples revealed that all the membrane polypeptides seen by staining with Coomassie blue were visualised by fluorography. Other studies revealed the applicability of the approach used for producing highly labelled cell sap and serum proteins. The overall results demonstrate the suitability of L-[35S]methionine administered in vivo for producing mouse liver ER membrane polypeptides of relatively high radioactivity and are consistent with a rapid conversion of RER to SER by ribosome detachment or membrane flow.

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