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Dive into the research topics where Barbara A. Jakschik is active.

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Featured researches published by Barbara A. Jakschik.


Biochemical and Biophysical Research Communications | 1980

Calcium stimulation of a novel lipoxygenase.

Barbara A. Jakschik; Frank F. Sun; Lieh-hauh Lee; Maggie M. Steinhoff

Abstract Homogenates of rat basophilic leukemia (RBL-1) cells have a novel lipoxygenase which was stimulated by calcium in a concentration dependent fashion and inhibited by epinephrine. The major compounds formed from [14C]-arachidonic acid were identified by gas chromatography — mass spectrometry to be 5-hydroxyeicosatetraenoic acid and 5,12-dihydroxyeicosatetraenoic acid. Other compounds present in small amounts were 12-hydroxy- and 5,6-dihydroxyeicosatetraenoic acid. The stimulation by calcium of this pathway in basophils links it closely to the release reaction which is calcium dependent.


Journal of Clinical Investigation | 1994

Mast cell degranulation induced by type 1 fimbriated Escherichia coli in mice.

Ravi Malaviya; Elaine Ross; Barbara A. Jakschik; Soman N. Abraham

The strategic location of mast cells at the host-environment interface and their ability to release potent mediators of inflammation have suggested that these cells may play a pivotal role in host defense against bacterial infection. The ability of the opportunistic pathogen, Escherichia coli, to induce degranulation of mast cells obtained from the mouse peritoneum was investigated. We determined that unlike a mutant derivative deficient in the FimH subunit of the fimbriae or nonfimbriated E. coli, type 1 fimbriated E. coli induced mast cell degranulation in vitro. The magnitude of mast cell degranulation was directly proportional to the number of adherent bacteria on the cell surface in the initial period of the interaction. Using a mouse model of bacterial peritonitis, we demonstrated mast cell degranulation and histamine release by type 1 fimbriated bacteria in vivo. Furthermore, beads coated with FimH but not with FimA, the major subunit of type 1 fimbriae, evoked mast cell release of histamine in vivo in amounts comparable to that elicited by type 1 fimbriated E. coli. These studies reveal that mast cells can be degranulated by interaction with type 1 fimbriated E. coli and that FimH, the mannose-binding component of the fimbriae, is a potent mast cell stimulant.


Journal of Clinical Investigation | 1991

Augmentation of reverse arthus reaction by mast cells in mice.

Yan Zhang; Bernard F. Ramos; Barbara A. Jakschik

Immune complex-induced injury is an important pathogenic factor in antibody-mediated nephritis, systemic lupus erythematosus, rheumatoid arthritis, and other diseases. In this study we investigated the role mast cells in immune complex-mediated injury in mouse skin. Reverse Arthus reaction was induced in mast cell-deficient WBB6F1-W/Wv mice and their congenic controls (WBB6F1(-)+/+). Serial skin sections were evaluated for neutrophil infiltration, edema, and hemorrhage. In WBB6F1-W/Wv mice the neutrophil influx was only 40% and edema 60% of that in congenic controls. Hemorrhage was also significantly reduced in the mast cell-deficient mice. After mast cell reconstitution, the magnitude of the reaction in WBB6F1-W/Wv was equivalent to that in WBB6F1(-)+/+ mice. Mast cell release in reverse Arthus reaction was evaluated by measuring fluorescence intensity after avidin-FITC staining of mast cell granules. There was a 70% decrease in fluorescence intensity. The 5-lipoxygenase inhibitor A-63162 significantly decreased neutrophil accumulation (40%), edema (60%), and hemorrhage in WBB6F1(-)+/+, but not in mast cell-deficient mice. Mast cell reconstitution of WBB6F1-W/Wv mice restored the effect of A-63162. The results indicate that mast cells and their mediators, including leukotrienes, make an important contribution to reverse Arthus reaction.


Prostaglandins | 1980

Fatty acid structural requirements for leukotriene biosynthesis

Barbara A. Jakschik; Alvin R. Sams; Howard Sprecher; Philip Needleman

Utilizing a variety of fatty acids, differing in chain length, degree and position of unsaturation, we investigated the substrate specificity for the enzymatic production of biologically active slow reacting substances (SRS) and of the other leukotrienes. A cell-free enzyme system obtained from RBL-1 cells was used in this study. The primary structural requirement observed for the conversion by this lipoxygenase enzyme system was a delta 5,8,11 unsaturation in a polyenoic fatty acid. Such fatty acids as 20:4 (5,8,11,14) 20:5 (5,8,11,14,17), 20:3 (5,8,11), 19:4 (5,8,11,14) and 18:4 (5,8,11,14) were readily converted to compounds that comigrated with 5-HETE and 5,12-DiHETE and to biologically active SRS. Chain length did not have an influence on the formatin of these hydroxyacids. Fatty acids with the initial unsaturation at delta 4, delta 6, delta 7, or delta 8 were a poor substrate for the leukotriene enzyme system. Therefore, this lipoxygenase pathway in leukocytes is quite different from the lipoxygenase in platelets which does not exhibit this specificity.


Journal of Clinical Investigation | 1974

Profile of Circulating Vasoactive Substances in Hemorrhagic Shock and Their Pharmacologic Manipulation

Barbara A. Jakschik; Garland R. Marshall; Janet L. Kourik; Philip Needleman

(a) Hemorrhage in dogs (to 45-50 mm Hg) was associated with a 10-fold increase in plasma renin activity (PRA) which remained elevated throughout the time-course of shock including the irreversible (decompensation) stage. The presence of angiotensin II (AII) in arterial blood was demonstrated by the bloodbathed organ technique and confirmed by blockade with specific AII antagonists (cysteine(8)-AII or isoleucine(8)-AII). The contribution of AII to systemic peripheral resistance during hemorrhage shock in dogs was established by administering AII antagonists which immediately cause a further fall in blood pressure.(b) Plasma catecholamines (CA) steadily increased during hemorrhage and peaked during compensation (a 100-fold increase). The CA decreased progressively during decompensation.(c) Prostaglandin (PG) E-like material was observed in arterial blood for 15-60 min (after hemorrhage); the peak arterial concentration was 2.6 ng/ml blood. Indomethacin (i.v., before 80% of maximum bleedout): (i) confirmed the presence of PGE, (ii) increased blood pressure, and (iii) increased blood loss.(d) Thus: peripheral resistance during hemorrhagic shock seems temporally correlated with blood CA levels (and not PRA), and the renin-AII system contributes to the maintenance of vascular resistance and may markedly decrease perfusion of organs, such as kidney; the administration of the proper combination of specific antagonists of vasoconstrictor humoral substances may radically improve organ perfusion and could contribute to ultimate recovery from hemorrhagic shock.


Prostaglandins | 1978

Arachidonic acid metabolism in rat basophilic leukemia (RBL-1) cells☆

Barbara A. Jakschik; L.H. Lee; G. Shuffer; Charles W. Parker

Abstract Rat basophilic leukemia (RBL-1) cells metabolized arachidonic acid through more than one enzymatic pathway. The major cyclooxygenase product was prostaglandin (PG) D2 as established by chromatographic and chemical behavior and the effect on platelet aggregation. PGD2 formation from exogenous arachidonic acid was inhibited by indomethacin, 1 μg/ml. RBL-1 incubated with exogenous arachidonic acid also formed SRS-A the synthesis of which was not inhibited by indomethacin. However, the SRS-A activity was blocked by the specific receptor antagonist FPL 55712. [14C]arachidonic acid was effectively incorporated into the phospholipids of RBL-1 cells. Challenge of such prelabelled cells or unlabelled cells with A 23187 caused release of PGD2, SRS-A and another presently unidentified product. However, with A 23187 as a stimulus, the RBL-1 cyclo-oxygenase could not be blocked by low concentrations of indomethacin. This work further substantiates our earlier findings that SRS-A formed from arachidontic acid is not a cyclooxegenase product.


Prostaglandins | 1983

Characterization of leukotriene A4 and B4 bioysnthesis

Barbara A. Jakschik; Christine G. Kuo

We have studied LTA4 and LTB4 synthesis in a cell-free system from RBL-1 cells. All the enzymes leading to the formation of LTB4 from arachidonic acid are localized in the soluble fraction (100,000 x g supernatant) of these cells. The formation of LTA4 and LTB4 is complete by 10 min. When we varied the arachidonic acid concentration from 1 to 300 microM, the synthesis of LTB4 leveled off at 30 microM and of LTA4 at 100 microM while 5-HETE had not reached a plateau at 300 microM. This enzyme system has the capacity to generate relatively large amounts of 5-HETE and LTA4 and only a relatively small amount of LTB4. Therefore, the rate limiting step is not the 5-lipoxygenase, the first step in the pathway, but the conversion of LTA4 to LTB4. This is in contrast to cyclooxygenase pathway where the first step is rate limiting. A second addition of arachidonic acid at submaximal concentration for LTA4 synthesis did not produce any additional LTA4 or LTB4. Further study of this phenomenon showed that the 5-lipoxygenase and LTA-synthase were inactivated with time by preincubation with arachidonic acid and that peroxy fatty acids seem to be the inactivating species.


Biochimica et Biophysica Acta | 1985

Arachidonic acid metabolism in isolated pancreatic islets: IV. Negative ion-mass spectrometric quantitation of monooxygenase product synthesis by liver and islets

John Turk; Bryan A. Wolf; P G Comens; Jerry R. Colca; Barbara A. Jakschik; Michael L. McDaniel

Deuterium-labelled standards of four regionally isomeric epoxyeicosatrienoic acids (EETs) and their hydrolysis products, the dihydroxyeicosatrienoic acids (DHETs), have been prepared and analyzed by capillary column gas chromatography (GC)-negative ion (NI)-methane chemical ionization (MCI)-mass spectrometry (MS) as the pentafluorobenzyl esters. As little as 40 pg of these compounds were readily visualized by these methods, and the deuterium-labelled standards were used in a stable isotope dilution mass spectrometric assay which was linear from near the detection limit over several orders of magnitude. NADPH-dependent synthesis of both EETs and DHETs from arachidonate by hepatic microsomal cytochrome P-450-mono-oxygenase activity was demonstrable with these methods and was significantly suppressed by the compound BW755C (500 microM), but not by eicosa-5,8,11,14-tetraynoic acid (ETYA, 20 microM) or by nordihydroguaiaretic acid (NDGA, 50 microM). All three compounds suppress glucose-induced insulin secretion and 12-hydroxyeicosatetraenoic acid (12-HETE) synthesis by isolated pancreatic islets with similar concentration dependence. Microsomes derived from isolated pancreatic islets synthesized less than 3% of the EET and DHET compounds as a comparable amount of hepatic microsomes. Intact islets synthesized less than 3% by mass of the EET and DHET compounds compared to the mass of 12-HETE produced by the islets. Islets also failed to convert 3H-labelled arachidonate to 3H-labelled EETs or DHETs under conditions where conversion to [3H]12-HETE and to [3H]prostaglandin E2 (but not to [3H]leukotriene C4, D4, or E4) was clearly demonstrable. Neither exogenous EETs nor leukotriene C4 stimulated insulin secretion from the isolated islets or reversed the suppression of glucose-induced secretion by the lipoxygenase inhibitor BW755C. The cytochrome P-450-monooxygenase inhibitor, metyrapone (50 microM), did not influence insulin secretion from the isolated islets under conditions where the lipoxygenase inhibitor, NDGA, suppressed glucose-induced secretion. These observations argue against the recently suggested hypothesis that EETs derived from arachidonate by monooxygenase action participate in glucose-induced insulin secretion by isolated pancreatic islets.


Biochimica et Biophysica Acta | 1980

Enzymatic formation of prostaglandin D2 by rat basophilic leukemia cells and normal rat mast cells

M.M. Steinhoff; L.H. Lee; Barbara A. Jakschik

It has been shown that the major cyclooxygenase product in rat basophilic leukemia (RBL-1) cells and in normal rat mast cells is prostaglandin D2. In RBL-1 cells, prostaglandin D2 is isomerase activity was found in the 150 000 X g microsomal pellet as well as the supernatant fraction. Incubation of RBL-1 microsomes with arachidonic acid without cofactors yielded 17.5 +/- 2% prostaglandin E2 and 9.1 +/- 1.4% prostaglandin D2. The cyclooxygenase activity was enhanced (25%) by epinephrine and the addition of reduced glutathione led to a marked increase in prostaglandin D2 synthesis (3-fold). Incubations with arachidonic acid, glutathione and epinephrine gave the maximum conversion to prostaglandin D2, yielding 7 +/- 0.4% prostaglandin E2 and 35.6 +/- 3.5% prostaglandin D2. Incubations with [14C]prostaglandin H2 to bypass cyclooxygenase confirmed the presence and glutathione dependence of the prostaglandin D2 isomerase in the microsomal fraction and also revealed the presence of the same enzyme in the 150 000 X g supernant. In contrast to RBL-1 cells, incubations of microsomes and supernatant from normal rat mast cells with [14C]-arachidonic acid and [14C]prostaglandin H2 localized the prostaglandin D2 isomerase activity in the soluble fraction. Similar to the enzyme in the RBL-1 cells, the mast cell enzyme was glutathione dependent.


Progress in Lipid Research | 1981

Fatty acids as sources of potential “magic bullets” for the modification of platelet and vascular function

Philip Needleman; Angela Wyche; Louise E. Leduc; S.K. Sankarappe; Barbara A. Jakschik; Howard Sprecher

Platelet cyclooxygenase exhibits a pronounced structural specificity whereas the lipoxygenase does not. Agonist recognition by platelets appears to be highly discriminatory. Endoperoxides apparently act on different receptors than do the thromboxanes and furthermore, thromboxane receptor recognition and/or activation must differ in blood vessels and platelets. The α-chain of the fatty acid metabolites profoundly influences receptor recognition without apparent influence of substrate affinity by the synthetic enzymes. The availability of inactive products or of partial agonists for the vascular and platelet receptors could lead to the development of selective receptor agonists and antagonists. Obviously there would be a considerable advantage in developing platelet-specific receptor analogs which do not influence smooth muscle receptors. Fatty acids which possess a Δ5 unsaturation are readily converted by a calcium-dependent, cell-free enzyme system into mono- and dihydroxy fatty acids. However, in the presence of glutathione, this enzyme system completely assembles the biologically active slow-reacting substance of anaphylaxis (now termed leukotrienes C and D). Thus, arachidonic acid (5, 8, 11, 14), eicosapentaenoic acid (5, 8, 11, 14, 17), and 20:3 (5, 8, 11; which accumulates during essential fatty acid deficiency) all are excellent substrates for the synthesis of potent biologically active leukotrienes. Eicosapentaenoic acid (EPA, 5, 8, 11, 14, 17-) can serve as a prototype for the utilization of a fatty acid as a dietary strategy for the manipulation of certain disease processes. EPA as well as other members of the ω3 fatty acid family are effective antagonists of arachidonic acid metabolism (both exogenous or endogenous) by platelet cyclooxygenase. A substitution of EPA or possibly its precursor (9, 12, 15-octadecatrienoic acid, α-linolenic acid) in the diet would be expected to lead to both an inhibition of arachidonic acid metabolism and the lowering of endogenous arachidonate in tissue (e.g., platelets) lipids. The net anticipated result would be a marked reduction in the generation of PGH2 and thromboxane A2 which cause platelet aggregation. A preliminary clinical trial supporting this hypothesis has recently appeared. However, the discovery of the ease of conversion of EPA into the bronchoconstrictor leukotrienes demands appropriate caution and additional experimentation prior to widespread dietary supplementation.

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Philip Needleman

Washington University in St. Louis

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Bernard F. Ramos

Washington University in St. Louis

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Charles W. Parker

Washington University in St. Louis

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Christine G. Kuo

Washington University in St. Louis

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Yan Zhang

Washington University in St. Louis

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Aubrey R. Morrison

Washington University in St. Louis

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Eugene M. Johnson

Washington University in St. Louis

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John Turk

Washington University in St. Louis

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