Search PubMed⌕ Search

Biomedical subjects

L Birnbaumer

Publications and source records attributed to L Birnbaumer.

At least 235 records · Page 13Linked to original sources
PubMed1983

Effects of estradiol treatment on rabbit luteal adenylyl cyclase: loss of luteinizing hormone receptors and attenuation of the regulatory N component activity.

We have reported previously that exogenously administered estradiol (E2) results in attenuation of the LH response of rabbit luteal adenylyl cyclase (approximately 50% less activity than control). This was accompanied by a much lesser reduction in the response of the system to the beta-adrenergic agonist isoproterenol (approximately 35% less activity than control). The purpose of the study reported here was to determine if the decreased responsiveness of adenylyl cyclase was the result of altered hormone receptor levels. To this end, hormone receptors were assessed by Scatchard analysis of specific binding. We confirmed that 4-day E2 treatments, which elevated serum E2 levels from 5 to 21 pg/ml. resulted in decreases in LH- and isoproterenol-stimulated adenylyl cyclase activities by 52% and 20%, respectively. In addition, we found that NaF-stimulated activity was also decreased by 20%. Basal adenylyl cyclase activity was unaffected. Upon assessment of the LH and beta-adrenergic receptor levels in luteal membranes, we found that E2 treatment resulted in marked reduction in LH receptor levels to 28% of the control value without changes in the levels of beta-adrenergic receptors. In view of the concomitant changes in the responsiveness of luteal membranes to isoproterenol and NaF, we determined whether E2 treatment affected luteal membrane levels of the stimulatory nucleotide-binding regulatory component (N) of adenylyl cyclase. N component activity was measured using a reconstitution assay that employs the stimulatory N component-deficient cyc- variant of the S49 mouse lymphoma cell line as an acceptor for luteal N component. Using this assay, we found that luteal membrane N component activity was reduced by 20-25% in E2-treated rabbits compared to that in control rabbits. All of the changes noted above were statistically significant. The results uncovered two heretofore unrecognized effects of E2 treatment: 1) loss of LH receptors, and 2) modification of the membrane component responsible for coupling of stimulatory receptors to the catalytic component of adenylyl cyclase.

Adenylyl Cyclases↗
PubMed1983

Human chorionic gonadotropin-induced heterologous desensitization of adenylyl cyclase from highly luteinized rat ovaries: attenuation of regulatory N component activity.

We injected hCG into superovulated rats on the seventh day of pseudopregnancy and confirmed previous findings that this results in both homologous desensitization of luteal adenylyl cyclase (loss of responsiveness to LH) and heterologous desensitization of the same adenylyl cyclase system (partial loss of responsiveness to catecholamines), and that these changes are associated with the loss of available unoccupied LH receptors (down-regulation) but not with any discernible loss of beta-adrenergic receptors. We tested the hypothesis that the heterologous component of the above changes might be due to alterations in the function of the nucleotide-binding N component of adenylyl cyclase that intervenes between receptors and catalytic units of adenylyl cyclase. This was done by assessing N component activity in reconstitution assays that measured the capacity of luteal N to mediate, in cyc- S49 lymphoma membranes, stimulation of adenylyl cyclase independently by the guanine nucleotide guanylyl imidodiphosphate, by NaF, or by the lymphoma membrane beta-adrenergic receptor. By all of these modes of assay, heterologous desensitization of luteal adenylyl cyclase to beta-adrenergic stimulation was found to be associated with a proportionally similar decrease in N component activity. This change in N component activity could be due to either quantitative or qualitative alterations. It is speculated that if the change is of a qualitative nature, the alteration may be a cAMP-dependent phosphorylation reaction of one of the subunits of the N component.

Adenylyl Cyclases↗
PubMed1983

Luteal adenylyl cyclase does not develop sensitivity to desensitization by human chorionic gonadotropin in the absence of nonluteal ovarian tissue.

There is evidence suggesting that the mere presence of a hormone-responsive adenylyl cyclase system in a tissue may not be sufficient for desensitization to occur since phosphorylation reactions might also be involved. The purpose of this study was to determine if luteal tissue in the absence of other ovarian tissues would desensitize to human CG (hCG). One or both ovaries were removed from rabbits 5 h before hCG-induced ovulation and the periovulatory follicles were transplanted underneath the kidney capsule where they formed ectopic corpus luteum [or corpora lutea (CL)]. Rabbits which were bilaterally ovariectomized received estradiol implants at the time of ovariectomy to maintain control serum estradiol concentrations. On day 7 of pseudopregnancy, the rabbits were injected with saline (control) or with 75 IU hCG and were killed 24 h later at which time ovarian and ectopic CL progesterone content and adenylyl cyclase activity were assessed. As expected, in ovarian CL there was decreased LH-responsive adenylyl cyclase (69% relative to control) and a correspondingly decreased luteal progesterone content (40% relative to control). In the same rabbits, the ectopic CL showed much the same pattern of response as the ovarian CL but perhaps to a slightly lesser extent (decreases relative to control of 59% in adenylyl cyclase response to LH and 29% in progesterone content). However, in rabbits with ectopic CL only, the luteal tissue showed no change either in hormone-responsive adenylyl cyclase activity or in progesterone content. Similarly, binding of radiolabeled hCG to luteal membranes 24 h after hCG was almost totally absent in ovarian CL, was decreased by 50% in ectopic CL with one ovary present, and was unaltered in ectopic CL of bilaterally ovariectomized rabbits. These data suggest that nonluteal ovarian tissue may be required for the induction in CL of the appropriate protein kinases for the proposed phosphorylations involved in adenylyl cyclase desensitization.

Adenylyl Cyclases↗
PubMed1982

Guanine nucleotide inhibition of cyc- S49 mouse lymphoma cell membrane adenylyl cyclase.

Cyc- S49 mouse lymphoma cell membranes contain an adenylyl cyclase system which is deficient in the regulatory properties characteristic of a stimulatory guanine nucleotide-binding regulatory component (Ns), such as enhancement of activity in the presence of GTP, GTP analogues, and NaF. Detailed kinetic analysis of cycl- adenylyl cyclase showed, however, that it is not unresponsive to these agents, for their addition to assays elicited inhibitory effects. Inhibition of cyc- activity was seen in 11 different membrane preparations obtained from two different strains and was observable both in the absence and presence of the strongly stimulatory diterpene forskolin. The GTP analogues GTP gamma S and guanyl-5'-yl imidodiphosphate caused a maximum of 60% inhibition with IC50 values of 2 and 12 nM, respectively. GTP itself was less potent than its analogues, with an IC50 of 100 mM, and elicited less inhibition as well (a maximum of 25%). Cholera toxin treatment of cyc- S49 cell membranes, under conditions which appeared to maximally activate the adenylyl cyclase system of wild type S49 cell membranes, had no effect on inhibition of catalytic activity. Our results indicate the presence in cyc- S49 cell membranes of a guanine nucleotide-binding component which is inhibitory to adenylyl cyclase activity (Ni). This suggests (a) that these membranes cannot be considered as completely deficient of adenylyl cyclase guanine nucleotide-binding regulatory components, and (b) that these membranes offer a unique opportunity to study Ni-mediated effects of guanine nucleotides and fluoride in the functional absence of Ns-mediated effects of these agents.

Adenylyl Cyclase Inhibitors↗
PubMed1982

Hormone receptor modulates the regulatory component of adenylyl cyclase by reducing its requirement for Mg2+ and enhancing its extent of activation by guanine nucleotides.

N-Ethylmaleimide treatment of rat liver plasma membranes results in an adenylyl cyclase (EC 4.6.1.1) system that shows no measurable cyclizing activity but retains both an active glucagon receptor and a receptor-sensitive regulatory component N as assessed by reconstitution into cyclase-negative (cyc-) membranes from S49 murine lymphoma. Treatment of such N-ethylmaleimide-treated membranes, termed C- liver membranes, with guanosine 5'-[gamma-thio]triphosphate (GTP[gamma S] ) and Mg2+, followed by the removal of GTP[gamma S] by washing, yields an activated N which upon mixing with cyc- S49 membranes reconstitutes the cyc- S49 membrane adenylyl cyclase in the absence of added GTP[gamma S]. It was found that GTP[gamma S] activation of the N at saturating concentrations of GTP[gamma S] is slow at low Mg2+ concentration and accelerated by increasing Mg2+ concentrations. Addition of glucagon during the activation results in a lowering of the Mg2+ requirement for full activation from 25 mM to around 10 muM and in concomitant increases in both the rate and the extent of N activation. In contrast to its dramatic effect on Mg2+ requirement, glucagon has little (less than 2-fold) effect on the GTP[gamma S] requirement of N activation. These experiments indicate that the glucagon receptor facilitates activation of N by: (i) decreasing the apparent Km of N for Mg2+, and (ii) increasing the extent of activation that can be elicited by saturating concentrations of guanine nucleotide. It is postulated that the mechanism by which Mg2+ and receptors facilitate N activation involves dissociation of n alpha activated ADP-ribosylatable subunits (with guanine nucleotide bound to them) from n beta non-ADP-ribosylatable subunits (with receptor and Mg2+ bound to them).

Adenylyl Cyclases↗
PubMed1982

Temporal characteristics of gonadotropin interaction with rabbit luteal receptors and activation of adenylyl cyclase: comparison to the mode of action of catecholamine receptors.

The temporal characteristics of gonadotropin (LH and hCG) and catecholamine interaction with their luteal receptors and activation of adenylyl cyclase were studied in rabbit luteal membranes. studies on hormone-receptor interaction showed that, once bound, [125I]iodo-hCG dissociated from its receptor very slowly. If excess LH was added 30 min after the initiation of [125I]iodo-hCG binding, 85% of the [125I]iodo-hCG bound at 30 min was still bound to the luteal receptors 4.5 h later. The rate of dissociation of [125I]iodo-hCG from its receptor was not altered by 100 microM GTP, 2 mM MgCl2, or GTP plus MgCl2. The slow rate of [125I]iodo-hCG dissociation observed at 30 min was not due to a time-dependent change in the hormone-receptor complex, as the dissociation of [125I]iodo-hCG was equally slow 5 min after the initiation of the binding reaction. Studies on the activation of luteal adenylyl cyclase by LH showed that stimulation by 1 microgram/ml ovine LH (oLH) could be prevented but, once initiated, could not be reversed by antiserum to oLH. This indicates that once bound to the rabbit luteal LH receptor, oLH causes persistent activation of rabbit luteal adenylyl cyclase. In contrast, the activation of luteal adenylyl cyclase by 1 microM isoproterenol could be completely reversed by the addition of 50 nM propranolol 5 min after the initiation of the reaction. The inhibitory effect of the propranolol could be completely overcome by the addition of excess isoproterenol, indicating that catecholamine binding to its luteal beta-receptor is readily reversible. Thus, there appears to be a basic difference in the mechanism by which the gonadotropins and catecholamines interact with their receptors and activate the rabbit luteal adenylyl cyclase.

Adenylyl Cyclases↗
PubMed1981

Studies on the mechanism of luteinizing hormone-induced desensitization of the rabbit follicular adenylyl cyclase system in vitro.

In vitro studies were conducted to evaluate the possible mechanisms of LH-induced desensitization of the rabbit follicular adenylyl cyclase (AC) system. We tested the effects of cAMP, dibutyryl cAMP, and inhibitors of various cellular functions on LH-stimulated AC activity as well as the reversibility of AC desensitization. Refractoriness of the AC to LH was induced by a1 1- or 2-h incubation of Graafian follicles with 10 microgram/ml LH. We fund that the initial 60-min phase of AC desensitization to LH in Graafian follicles was not prevented by a 60-min preincubation of follicles with 11 microM puromycin, 30 microM cycloheximide, 8 microM actinomycin D, 5 microgram/ml cytochalasin B, 50 microM colchicine, or 1 or 10 mM trinitrophenol or by a 90-min preincubation of follicles with 50 microM colchicine. We evaluated the effects of cAMP and dibutyryl cAMP on LH-stimulated AC activity by incubating Graafian follicles with these nucleotides for 30-min to 4 h. While LH-stimulated AC activity was not significantly reduced in follicles which had been incubated 30-min or 1-h with either nucleotide, 2 h incubations resulted in significant reductions in LH-stimulated AC activity, and 4-h incubations promoted a complete refractoriness of the LH-stimulable AC. cAMP also caused desensitization of the FSH-stimulable AC in 4-h incubations, but not in the 1-h incubations. Lastly, once the follicular AC was desensitized to LH, neither 4-guanylyl imidodiphosphate nor ATP could reverse desensitization. These results indicate that AC desensitization in rabbit Graafian follicles is biphasic event. The initial 60-min phase is not mediated by cAMP, RNA, or protein synthetic events, by energy-requiring events inhibited by trinitrophenol, or by microtubule- or micro-filament-associated processes. A secondary phase occurs within 2-h and appears to be mediated, at least in part, by cAMP.

Adenylyl Cyclases↗
PubMed1981

Developmental changes in the hormonal regulation of rat testis Sertoli cell adenylyl cyclase.

The stimulatory effects of FSH on Sertoli cell functions such as cAMP accumulation, protein kinase activation, and RNA and protein synthesis wane during testis maturation. However, FSH receptors increase with age and addition of cAMP stimulates these biochemical events in Sertoli cells from animals of any age. In order to determine if this loss of responsiveness to FSH was due to an inability to stimulate adenylyl cyclase, the hormonal responsiveness of this enzyme was investigated as a function of testicular development. In agreement with intact cell studies, adenylyl cyclase activity was found to be stimulated by FSH 2- to 3-fold in homogenates of testes from immature (5-20 days of age) Sertoli cell-enriched rats, while no stimulation of the enzyme by FSH was observed in similar homogenates from Sertoli cell-enriched animals 20 days of age or older. The possibility of a decrease in enzyme sensitivity to the gonadotropin as a function of maturation ws ruled out by dose-response studies. Catalytic activity of the enzyme was retained with increasing animal age as evidenced by the ability of fluoride (10 mM) to stimulate basal activity 4-fold. Hormonal responsiveness of the Sertoli cell adenylyl cyclase of mature animals could be restored, however, either by addition of the nonmetabolizable guanosine 5'-triphosphate analog, 5'-guanylyl-imidodiphosphate to homogenates or by preparation of membrane particles. We found that 5'-guanylyl-imidodiphosphate selectively potentiated FSH effects on cyclase in testicular homogenates from mature animals while having no effect on the relative degree of hormone stimulation in homogenates from immature animals, and that in contrast to homogenates, testicular membrane preparations retain their FSH responsiveness upon animal maturation.

Adenylyl Cyclases↗
PubMed1981

Effects of withdrawal of exogenous estradiol from pseudopregnant rabbits: transient nature of loss of luteal function and reversal of estradiol-induced suppression of luteinizing hormone-responsive adenylyl cyclase.

We have reported in recent studies that exogenous estradiol (E2) suppresses luteal LH-responsive adenylyl cyclase activity in pseudopregnant rabbits. The purpose of the present study was to determine whether this suppression is reversible. High or low level E2-filled Silastic capsules or empty capsules were sc implanted in day 5 pseudopregnant rabbits. On day 8 of pseudopregnancy, the high level E2 implants were either sham replaced, replaced with low level E2 implants, or replaced with empty capsules. The low level E2 implants and empty capsules were sham replaced. Animals from each of the five resulting groups were killed on days 9-12 of pseudopregnancy (1, 2, 3, and 4 days postimplant manipulation). As previously reported using an intermittent injection protocol, exogenous E2 had little effect upon serum progesterone concentrations. Both high and low level E2 implants suppressed the luteal LH-responsive adenylyl cyclase, but the suppression due to the low level E2 implants was not as great as that for the high level E2 implants. Within 24 h of switching from high to low level E2 implants, LH-responsive adenylyl cyclase activity increased from the level found for animals with high level E2 throughout to that found for animals with low level E2 throughout. Total withdrawal of exogenous E2 resulted in a precipitous fall in serum progesterone concentrations, as predicted by previous studies. However, within 4 days of withdrawal, both serum progesterone and luteal LH-responsive adenylyl cyclase activity had returned to control values. E2 implants also suppressed serum LH concentrations and follicular LH-responsive adenylyl cyclase activities. Both of these effects were reversed within 24-48 h after implant withdrawal. We conclude, therefore, that effects of exogenous E2 are reversible and that the previously reported E2-induced dependency upon exogenous E2 is related to the experimental protocol used.

Adenylyl Cyclases↗
PubMed1981

[125I]iodopindolol: a new beta adrenergic receptor probe.

When utilizing iodohydroxybenzylpindolol (IHYP) as an adrenergic receptor probe in muscle membrane systems, the data demonstrated an unacceptably high nonspecific binding component. Bearer et al. have reported that chloramine-T induced iodination of hydroxybenzylpindolol (HYP) results in the incorporation of iodine into the indole ring rather than into the phenolic moiety as noted previously by others. These results suggest that pindolol itself can also be iodinated. Therefore, the usefulness of carrier free 125I-labeled iodopindolol (IPIN) as an adrenergic receptor probe was investigated. Using between 0.01 nM and 0.1 nM [125I]IPIN in two different muscle membrane systems, we found the nonspecific binding component to be 10% or less of total binding. When [125I]IPIN was used with membranes prepared from rat skeletal muscle, we found it to interact with a single set of high affinity binding sites (KD = 0.13 +/- 0.01 nM) with the characteristics of beta adrenergic receptors and a density of 48.5 fmoles/mg protein. IPIN binding was also studied with purified dog cardiac sarcolemma. A single set of binding sites was detected having a KD of 1.64 +/- 0.5 nM; the density of these sites was 289 fmoles/mg membrane protein. [125I]IPIN may be a useful probe for the beta adrenergic receptor of tissues in which [125I]IHYP and other beta adrenergic receptor probes have a non-specific binding component which approaches that of the specific binding component.

Animals↗