ALBERT

All Library Books, journals and Electronic Records Telegrafenberg

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
  • Life and Medical Sciences  (4)
Collection
Publisher
Years
  • 1
    ISSN: 0730-2312
    Keywords: forskolin ; cholera toxin ; pertussis toxin ; interleukin-2 ; T lymphocyte ; G protein ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: The Nb2 T lymphoma is unique in that these lymphocytes proliferate in response to prolactin as well as in response to interleukin-2. In this study, we have examined the responsiveness of the adenylate cyclase system in Nb2 cells and the role of this signaling system in regulating proliferation and protein phosphorylation. An analog of cAMP inhibited prolactin-stimulated proliferation and blocked a prolactin-induced decrease in protein phosphorylation. Forskolin, a potent activator of adenylate cyclase in T lymphocytes, did not elevate cAMP levels in Nb2 cells and was not an effective inhibitor of prolactin-induced proliferation. In fact, one preparation of forskolin stimulated proliferation of quiescent Nb2 cells. Like forskolin, prostaglandin E2 did not stimulate cAMP production in Nb2 cells even though, it increased cAMP in a preparation of rat peripheral blood lymphocytes. Cholera toxin appeared to ADP-ribosylate a stimulatory guanine nucleotide-binding protein in Nb2 cells, but the toxin did not increase intracellular levels of cAMP nor was it a potent anti-mitogenic agent. Pertussis toxin, an agent that can increase cAMP production through suppression of the inhibitory guanine nucleotide-binding protein, exerted only minor anti-proliferative actions on prolactin-stimulated Nb2 cells. These data suggest that cAMP inhibits Nb2 cell proliferation and prolactin-induced changes in protein phosphorylation but that the adenylate cyclase system in our clone of Nb2 cells responds poorly to agents that normally increase cAMP.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 2
    ISSN: 0021-9541
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Rabbit red cells are separated by centrifuging them for one hour at 33,000 G in density gradient tubes of bovine serum albumin. The separation represented an equilibrium situation since rebanding experiments showed that the cells from a layer would again seek that density layer when recentrifuged in a new gradient tube. When rabbits were injected with 59Fe, the radioactive red cells at one day were nearly all light, but these labeled cells moved into the more dense layers over the next few days. This not only shows that the separation by density is discriminating but that some red cells became dense very quickly. Bearing in mind the problems of interpreting radioactive iron data because of the possibility of reutilization, it is tentatively concluded that dense red cells are not necessarily senescent red cells since these dense cells appear to persist for the normal life span of the rabbit red cell.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 3
    ISSN: 0095-9898
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Red cells from rabbits (reticulocyte count 1-2%) injected 4-6 days previously with Fe59 were centrifuged in isotonic hypodense media (plasma, buffer, saline) for 30 minutes at 1,600 G and layers were removed to achieve density fractionation. An important criterion of separation was the fractionation ratio (specific activity of hemoglobin in any layer/specific activity of hemoglobin in unfractionated blood) which indicated whether a layer contained mainly “new” or “old” red cells. The most important factor in enhancing the fractionation ratio was the centrifugal force, but time also had an effect. All isotonic media were essentially equivalent, but hypertonic media (sucrose) were quite poor. Dextran and PVP were also not good in promoting density separation. The exact degree of separation achieved by various combinations of conditions is documented, but no system achieves a true equilibrium, as shown by the fact that refractionation can split any fraction into subfractions of higher and lower hemoglobin specific activity. Upper layers were characterized by greater cell size, more reticulocytes, more free cholesterol, phospholipid, and ATP, and a faster rate of glycolysis. The distribution of Fe59 in the fractionated blood was followed serially for up to ten weeks, the most homogeneous distribution being seen only in the first week or two. After that the Fe59 was not sharply restricted to any density fraction. This suggested that the most significant density change takes place as the reticulocyte matures.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 4
    ISSN: 0749-503X
    Keywords: heat shock ; protein-DNA interactions ; transcriptional regulation ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: The C-terminal hydrophobic repeat (CTR) of heat shock transcription factor (HSF) has been proposed to regulate DNA binding by intramolecular interactions with the leucine zipper motifs present in the HSF trimerization domain. Schizosaccharomyces pombe provides a useful model organism for the study of the regulation of HSF DNA binding because, unlike Saccharomyces cerevisiae, S. pombe hsf is highly heat shock inducible for DNA binding and contains a clear homology to the CTR. We examined the role that the CTR plays in the regulation of S. pombe hsf by constructing isogenic strains bearing deletion and point mutations in the chromosomal copy of hsf. Surprisingly, we found that point mutation of key hydrophobic amino acids within the CTR, as well as full deletion of it, yielded factors that show normal binding at normal growth temperatures and full levels of heat-induced binding. Deletion of the CTR did, however, slightly lower the temperature required for maximal activation. In contrast, a large deletion of the C-terminus, which removes close to a third of the coding sequence, was deregulated and bound DNA at control temperature. Several of the deletion mutants were significantly reduced in their level of expression, yet they showed wild-type levels of DNA binding activity following heat shock. These experiments demonstrate that appropriate regulation of the DNA binding activity of S. pombe hsf is not solely dependent upon the CTR, and imply that a feedback mechanism exists that establishes proper levels of DNA binding following heat shock despite mutations that significantly alter levels of total hsf. © 1998 John Wiley & Sons, Ltd.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...