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1.
Braz J Med Biol Res ; 56: e12611, 2023.
Article in English | MEDLINE | ID: mdl-37792778

ABSTRACT

Islet transplantation represents a therapeutic option for type 1 diabetes (T1D). Long-term viability of transplanted islets requires improvement. Mesenchymal stromal cells (MSCs) have been proposed as adjuvants for islet transplantation facilitating grafting and functionality. Stem cell aggregation provides physiological interactions between cells and enhances the in situ concentration of modulators of inflammation and immunity. We established a hanging-drop culture of adult human skin fibroblast-like cells as spheroids, and skin spheroid-derived cells (SphCs) were characterized. We assessed the potential of SphCs in improving islet functionality by cotransplantation with a marginal mass of allogeneic islets in an experimental diabetic mouse model and characterized the secretome of SphCs by mass spectrometry-based proteomics. SphCs were characterized as multipotent progenitors and their coculture with anti-CD3 stimulated mouse splenocytes decreased CD4+ T cell proliferation with skewed cytokine secretion through an increase in the Th2/Th1 ratio profile. SphCs-conditioned media attenuated apoptosis of islets induced by cytokine challenge in vitro and importantly, intratesticular SphCs administration did not show tumorigenicity in immune-deficient mice. Moreover, SphCs improved glycemic control when cotransplanted with a marginal mass of allogeneic islets in a diabetic mouse model without pharmacological immunosuppression. SphCs' protein secretome differed from its paired skin fibroblast-like counterpart in containing 70% of up- and downregulated proteins and biological processes that overall positively influenced islets such as cytoprotection, cellular stress, metabolism, and survival. In summary, SphCs improved the performance of transplanted allogeneic islets in an experimental T1D model, without pharmacological immunosuppression. Future research is warranted to identify SphCs-secreted factors responsible for islets' endurance.


Subject(s)
Diabetes Mellitus, Experimental , Diabetes Mellitus, Type 1 , Hematopoietic Stem Cell Transplantation , Islets of Langerhans Transplantation , Islets of Langerhans , Humans , Mice , Animals , Adult , Islets of Langerhans/metabolism , Diabetes Mellitus, Type 1/therapy , Diabetes Mellitus, Type 1/metabolism , Diabetes Mellitus, Experimental/therapy , Diabetes Mellitus, Experimental/metabolism , Cytokines/metabolism
2.
Braz. j. med. biol. res ; 56: e12611, 2023. graf
Article in English | LILACS-Express | LILACS | ID: biblio-1513883

ABSTRACT

Islet transplantation represents a therapeutic option for type 1 diabetes (T1D). Long-term viability of transplanted islets requires improvement. Mesenchymal stromal cells (MSCs) have been proposed as adjuvants for islet transplantation facilitating grafting and functionality. Stem cell aggregation provides physiological interactions between cells and enhances the in situ concentration of modulators of inflammation and immunity. We established a hanging-drop culture of adult human skin fibroblast-like cells as spheroids, and skin spheroid-derived cells (SphCs) were characterized. We assessed the potential of SphCs in improving islet functionality by cotransplantation with a marginal mass of allogeneic islets in an experimental diabetic mouse model and characterized the secretome of SphCs by mass spectrometry-based proteomics. SphCs were characterized as multipotent progenitors and their coculture with anti-CD3 stimulated mouse splenocytes decreased CD4+ T cell proliferation with skewed cytokine secretion through an increase in the Th2/Th1 ratio profile. SphCs-conditioned media attenuated apoptosis of islets induced by cytokine challenge in vitro and importantly, intratesticular SphCs administration did not show tumorigenicity in immune-deficient mice. Moreover, SphCs improved glycemic control when cotransplanted with a marginal mass of allogeneic islets in a diabetic mouse model without pharmacological immunosuppression. SphCs' protein secretome differed from its paired skin fibroblast-like counterpart in containing 70% of up- and downregulated proteins and biological processes that overall positively influenced islets such as cytoprotection, cellular stress, metabolism, and survival. In summary, SphCs improved the performance of transplanted allogeneic islets in an experimental T1D model, without pharmacological immunosuppression. Future research is warranted to identify SphCs-secreted factors responsible for islets' endurance.

3.
J Matern Fetal Neonatal Med ; 32(1): 125-128, 2019 Jan.
Article in English | MEDLINE | ID: mdl-28868940

ABSTRACT

PURPOSE: Urinary tract infection (UTI) is defined as a common bacterial infection that can lead to significant morbidity such as stricture, fistula, abscess formation, bacteremia, sepsis, pyelonephritis, and kidney dysfunction with a mortality rates reported of 1% in men and 3% in women because of development of pyelonephritis. UTIs are more common in women and the 33% of them require antimicrobials treatment for at least one episode by the age of 24 years. UTIs are the most common infections observed during pregnancy and up to 30% of mothers with not treated asymptomatic bacteriuria may develop acute pyelonephritis which consequently can be associated to adverse maternal and fetal outcomes. All bacteriuria in pregnancy should be treated with antimicrobial treatments being safe for both the mother and the fetus. Approximately one every four women receives prescription of antibiotic treatment during pregnancy, nearly 80% of all the prescription medications during gestation. The use of fosfomycin to treat cystitis in pregnancy generally considered safe and effective. Even though use on antibiotics for urinary tract infections is considered generally safe for the fetus and mothers, this opinion is not based on specific studies monitoring the relationship of among urinary infections, consumption of antibiotics, and pregnancy outcomes. MATERIALS AND METHODS: On this basis we decided to analyze data from the database of our multicenter study PHYTOVIGGEST, reporting data from 5362 pregnancies, focusing on use of fosfomycin. Principal outcomes of pregnancy in women treated with fosfomycin were taken into consideration. RESULTS: Women who have been treated with urinary antibiotics during the pregnancy were 183. With respect to the total number of pregnancies of our sample, these women represented the percentage of 3.49% (187/5362). Analysis of different outcomes of pregnancy such as gestational age, neonatal weight, and neonatal Apgar index did not show any significant difference. At the same time, analysis of data of pregnancy complicancies (such as urgent cesarean delivery, use of general anesthesia, need to induce labor) did not show any difference in women taking fosfomycin during pregnancy and those not taking it. CONCLUSIONS: Our data, based on a large number of pregnancies, confirm the safety use of fosfomycin use in pregnancy.


Subject(s)
Anti-Bacterial Agents/therapeutic use , Fosfomycin/therapeutic use , Pregnancy Complications, Infectious/drug therapy , Pregnancy Outcome/epidemiology , Urinary Tract Infections/drug therapy , Adult , Female , Humans , Italy/epidemiology , Pregnancy
4.
Clin Exp Immunol ; 177(1): 149-60, 2014 Jul.
Article in English | MEDLINE | ID: mdl-24628444

ABSTRACT

Type 1 diabetes (T1DM) is a T cell-mediated autoimmune disease that selectively destroys pancreatic ß cells. The only possible cure for T1DM is to control autoimmunity against ß cell-specific antigens. We explored whether the natural compound curcumin, with anti-oxidant and anti-inflammatory activities, might down-regulate the T cell response that destroys pancreatic ß cells to improve disease outcome in autoimmune diabetes. We employed two accelerated autoimmune diabetes models: (i) cyclophosphamide (CYP) administration to non-obese diabetic (NOD) mice and (ii) adoptive transfer of diabetogenic splenocytes into NODscid mice. Curcumin treatment led to significant delay of disease onset, and in some instances prevented autoimmune diabetes by inhibiting pancreatic leucocyte infiltration and preserving insulin-expressing cells. To investigate the mechanisms of protection we studied the effect of curcumin on key immune cell populations involved in the pathogenesis of the disease. Curcumin modulates the T lymphocyte response impairing proliferation and interferon (IFN)-γ production through modulation of T-box expressed in T cells (T-bet), a key transcription factor for proinflammatory T helper type 1 (Th1) lymphocyte differentiation, both at the transcriptional and translational levels. Also, curcumin reduces nuclear factor (NF)-κB activation in T cell receptor (TCR)-stimulated NOD lymphocytes. In addition, curcumin impairs the T cell stimulatory function of dendritic cells with reduced secretion of proinflammatory cytokines and nitric oxide (NO) and low surface expression of co-stimulatory molecules, leading to an overall diminished antigen-presenting cell activity. These in-vitro effects correlated with ex-vivo analysis of cells obtained from curcumin-treated mice during the course of autoimmune diabetes. These findings reveal an effective therapeutic effect of curcumin in autoimmune diabetes by its actions on key immune cells responsible for ß cell death.


Subject(s)
Anti-Inflammatory Agents, Non-Steroidal/administration & dosage , Antioxidants/administration & dosage , Curcumin/administration & dosage , Dendritic Cells/drug effects , Diabetes Mellitus, Experimental/drug therapy , Diabetes Mellitus, Type 1/drug therapy , Th1 Cells/drug effects , Animals , Antigen Presentation/drug effects , Cells, Cultured , Dendritic Cells/immunology , Diabetes Mellitus, Experimental/immunology , Diabetes Mellitus, Type 1/immunology , Disease Models, Animal , Humans , Interferon-gamma/metabolism , Lymphocyte Activation/drug effects , Mice , Mice, Inbred BALB C , Mice, Inbred NOD , Mice, SCID , Mice, Transgenic , NF-kappa B/metabolism , T-Box Domain Proteins/genetics , T-Box Domain Proteins/metabolism , Th1 Cells/immunology , Transcriptional Activation/drug effects
5.
J Neurooncol ; 113(3): 385-96, 2013 Jul.
Article in English | MEDLINE | ID: mdl-23666203

ABSTRACT

Meningiomas, the most frequent benign intracranial and intraspinal types of tumors are normally removed by surgery. Complications can occur when the tumor is critically localized and cannot be completely removed or when comorbidities of the mostly elder patients increase the general surgical risk. Thus, alternate medical treatment concepts for the therapy of meningiomas would be desirable. Curcumin, the active ingredient of the spice plant Curcuma longa has shown anti-tumorigenic actions in many different types of tumors and therefore, its effect on growth and apoptosis of meningioma cells was studied in the present paper. In vitro, treatment of the human Ben-Men-1 meningioma cell line and of a series of 21 primary human meningioma cell cultures with curcumin (1-20 µM) strongly reduced the proliferation in all cases in a dose dependent manner. Cell cycle analysis by fluorescence-activated cell sorting showed growth arrest at G2/M phase, which was confirmed by demonstrating the corresponding modulation of proteins involved in G2/M arrest by immunoblotting and/or confocal laser microscopy. High dosages (20, 50 µM) of curcumin induced a significant increase of apoptosis in Ben-Men-1 and primary meningioma cell cultures as demonstrated by morphological changes of cell nuclei, DNA fragmentation, translocation of cell membrane associated phosphatidyl serine and the induction of apoptotic-acting cleaved caspase-3. Our results suggest that the multi-targeting drug curcumin has potent anti-tumorigenic actions in meningioma cells and might therefore be a putative candidate for the pharmacological treatment of meningiomas.


Subject(s)
Antineoplastic Agents/pharmacology , Apoptosis/drug effects , Cell Proliferation/drug effects , Curcumin/pharmacology , Meningeal Neoplasms/pathology , Meningioma/pathology , Blotting, Western , Cell Cycle/drug effects , Flow Cytometry , Fluorescent Antibody Technique , Humans , Meningeal Neoplasms/metabolism , Meningioma/metabolism , Tumor Cells, Cultured
6.
Clin Exp Immunol ; 171(2): 135-46, 2013 Feb.
Article in English | MEDLINE | ID: mdl-23286940

ABSTRACT

Type 1 diabetes mellitus (T1DM) results from death of insulin-secreting ß cells mediated by self-immune cells, and the consequent inability of the body to maintain insulin levels for appropriate glucose homeostasis. Probably initiated by environmental factors, this disease takes place in genetically predisposed individuals. Given the autoimmune nature of T1DM, therapeutics targeting immune cells involved in disease progress have been explored over the last decade. Several high-cost trials have been attempted to prevent and/or reverse T1DM. Although a definitive solution to cure T1DM is not yet available, a large amount of information about its nature and development has contributed greatly to both the improvement of patient's health care and design of new treatments. In this study, we discuss the role of different types of immune cells involved in T1DM pathogenesis and their therapeutic potential as targets and/or modified tools to treat patients. Recently, encouraging results and new approaches to sustain remnant ß cell mass and to increase ß cell proliferation by different cell-based means have emerged. Results coming from ongoing clinical trials employing cell therapy designed to arrest T1DM will probably proliferate in the next few years. Strategies under consideration include infusion of several types of stem cells, dendritic cells and regulatory T cells, either manipulated genetically ex vivo or non-manipulated. Their use in combination approaches is another therapeutic alternative. Cell-based interventions, without undesirable side effects, directed to block the uncontrollable autoimmune response may become a clinical reality in the next few years for the treatment of patients with T1DM.


Subject(s)
Autoimmunity/immunology , Dendritic Cells/immunology , Diabetes Mellitus, Type 1/immunology , Diabetes Mellitus, Type 1/therapy , Insulin-Secreting Cells/immunology , Stem Cell Transplantation/methods , T-Lymphocytes, Regulatory/immunology , Animals , Clinical Trials as Topic , Dendritic Cells/transplantation , Disease Models, Animal , Humans , Insulin/therapeutic use , Insulin-Secreting Cells/drug effects , Mice , Mice, Inbred NOD , Stem Cell Transplantation/trends , T-Lymphocytes, Regulatory/transplantation
7.
J Endocrinol ; 214(3): 389-98, 2012 Sep.
Article in English | MEDLINE | ID: mdl-22739211

ABSTRACT

Curcumin (diferuloylmethane), a polyphenolic compound derived from the spice plant Curcuma longa, displays multiple actions on solid tumours including anti-angiogenic effects. Here we have studied in rodent and human pituitary tumour cells the influence of curcumin on the production of hypoxia inducible factor 1α (HIF1A) and vascular endothelial growth factor A (VEGFA), two key components involved in tumour neovascularisation through angiogenesis. Curcumin dose-dependently inhibited basal VEGFA secretion in corticotroph AtT20 mouse and lactosomatotroph GH3 rat pituitary tumour cells as well as in all human pituitary adenoma cell cultures (n=32) studied. Under hypoxia-mimicking conditions (CoCl(2) treatment) in AtT20 and GH3 cells as well as in all human pituitary adenoma cell cultures (n=8) studied, curcumin strongly suppressed the induction of mRNA synthesis and protein production of HIF1A, the regulated subunit of the hypoxia-induced transcription factor HIF1. Curcumin also blocked hypoxia-induced mRNA synthesis and secretion of VEGFA in GH3 cells and in all human pituitary adenoma cell cultures investigated (n=18). Thus, curcumin may inhibit pituitary adenoma progression not only through previously demonstrated anti-proliferative and pro-apoptotic actions but also by its suppressive effects on pituitary tumour neovascularisation.


Subject(s)
Adenoma/drug therapy , Curcumin/pharmacology , Hypoxia-Inducible Factor 1, alpha Subunit/metabolism , Neovascularization, Pathologic/drug therapy , Pituitary Neoplasms/drug therapy , Vascular Endothelial Growth Factor A/metabolism , Adenoma/blood supply , Adenoma/metabolism , Animals , Antineoplastic Agents/pharmacology , Cell Hypoxia/drug effects , Cell Hypoxia/physiology , Cell Line, Tumor , Corticotrophs/cytology , Corticotrophs/drug effects , Corticotrophs/metabolism , Humans , Hypoxia-Inducible Factor 1, alpha Subunit/genetics , Lactotrophs/cytology , Lactotrophs/drug effects , Lactotrophs/metabolism , Mice , Pituitary Neoplasms/blood supply , Pituitary Neoplasms/metabolism , RNA, Messenger/metabolism , Rats , Somatotrophs/cytology , Somatotrophs/drug effects , Somatotrophs/metabolism , Vascular Endothelial Growth Factor A/genetics
8.
Front Horm Res ; 38: 158-164, 2010.
Article in English | MEDLINE | ID: mdl-20616507

ABSTRACT

Despite considerable progress, there is still no medical treatment available for some kinds of pituitary tumors, in particular hormone inactive adenomas and corticotroph pituitary tumors. Surgical removal or at least debulking of the tumor is the only option to treat these kinds of tumors apart from rarely applied radiotherapy. Moreover, treatment resistance is present in a considerable proportion of patients bearing pituitary tumors, for which medical treatment regimens are already available (prolactinomas, somatotroph adenomas). Thus, novel or improved medical treatment strategies would be desirable. Here, we summarize preclinical and clinical findings about the hormone and growth-suppressive action of various drugs, which will probably lead to novel future medical treatment concepts for pituitary tumors.


Subject(s)
Pituitary Neoplasms/drug therapy , Dopamine/analogs & derivatives , Dopamine/therapeutic use , Dopamine Agonists/therapeutic use , Humans , Interferon-gamma/therapeutic use , Somatostatin/analogs & derivatives , Somatostatin/therapeutic use , Tretinoin/therapeutic use
9.
Endocr Relat Cancer ; 16(4): 1339-50, 2009 Dec.
Article in English | MEDLINE | ID: mdl-19726538

ABSTRACT

Curcumin (diferuloylmethane) is the active ingredient of the spice plant Curcuma longa and has been shown to act anti-tumorigenic in different types of tumours. Therefore, we have studied its effect in pituitary tumour cell lines and adenomas. Proliferation of lactosomatotroph GH3 and somatotroph MtT/S rat pituitary cells as well as of corticotroph AtT20 mouse pituitary cells was inhibited by curcumin in monolayer cell culture and in colony formation assay in soft agar. Fluorescence-activated cell sorting (FACS) analysis demonstrated curcumin-induced cell cycle arrest at G2/M. Analysis of cell cycle proteins by immunoblotting showed reduction in cyclin D(1), cyclin-dependent kinase 4 and no change in p27(kip). FACS analysis with Annexin V-FITC/7-aminoactinomycin D staining demonstrated curcumin-induced early apoptosis after 3, 6, 12 and 24 h treatment and nearly no necrosis. Induction of DNA fragmentation, reduction of Bcl-2 and enhancement of cleaved caspase-3 further confirmed induction of apoptosis by curcumin. Growth of GH3 tumours in athymic nude mice was suppressed by curcumin in vivo. In endocrine pituitary tumour cell lines, GH, ACTH and prolactin production were inhibited by curcumin. Studies in 25 human pituitary adenoma cell cultures have confirmed the anti-tumorigenic and hormone-suppressive effects of curcumin. Altogether, the results described in this report suggest this natural compound as a good candidate for therapeutic use on pituitary tumours.


Subject(s)
Antineoplastic Agents/pharmacology , Curcumin/pharmacology , Pituitary Hormones/metabolism , Pituitary Neoplasms/drug therapy , Pituitary Neoplasms/pathology , Animals , Apoptosis/drug effects , Blotting, Western , Caspase 3/metabolism , Cell Cycle/drug effects , Cell Line, Tumor , Cell Proliferation/drug effects , Cyclin D1/metabolism , Cyclin-Dependent Kinase 4/metabolism , Flow Cytometry , Humans , Male , Mice , Mice, Nude , Pituitary Hormones/antagonists & inhibitors , Pituitary Neoplasms/metabolism , Rats
10.
Am J Transplant ; 6(6): 1297-311, 2006 Jun.
Article in English | MEDLINE | ID: mdl-16686754

ABSTRACT

Tolerance induction against donor allo-antigens (allo-Ag) remains one of the most challenging aspects of transplant immunology. The ability of dendritic cells (DC) to participate in immunity and tolerance makes them an excellent tool for tolerance induction. Here, we employed the immunosuppressive properties of apoptotic cells to deliver simultaneously an inhibitory signal and donor allo-Ag to recipient DC for treatment of allograft rejection. DC that captured apoptotic cells remained immature and activated deficiently anti-donor CD4(+) T cells that were unable to upregulate T-cell activation markers, to secrete IL-2 and IFN-gamma and to survive under homeostatic conditions due to low expression of Bcl-X(L), IL-7R and IL-15R. Administration of donor apoptotic cells decreased the systemic anti-donor T- and B-cell response and prolonged cardiac allograft survival in mice. The effect was donor specific and required the interaction of donor apoptotic cells with recipient quiescent CD8alpha(+) DC. When combined with CD40-CD154-blockade, administration of donor apoptotic cells resulted in indefinite graft survival mediated by generation of regulatory T cells. The use of the inhibitory effects of apoptotic cells on the anti-donor response provides a new approach to treat transplant rejection.


Subject(s)
CD4-Positive T-Lymphocytes/immunology , Dendritic Cells/immunology , Graft Survival/immunology , Heart Transplantation/immunology , Lymphocyte Depletion , Lymphocyte Transfusion , Animals , Apoptosis/radiation effects , Isoantibodies/blood , Lymph Nodes/immunology , Lymphocyte Culture Test, Mixed , Mice , Mice, Inbred BALB C , Mice, Inbred Strains , Models, Animal , Spleen/immunology , Transplantation, Homologous/immunology , Ultraviolet Rays
11.
Acta Biomed ; 76 Suppl 1: 27-8, 2005.
Article in English | MEDLINE | ID: mdl-16450504

ABSTRACT

The overall incidence of post-surgical infection actually amount to 3-10%, in different multicentric trial, although the data may underrepresent the true incidence of such infections owing to increase of day-surgery. Antibiotic prophylaxis rapresents the first choice in the management of surgical patients, which standardization and selection can determine a real protection for all the operating time. Standardization of intraoperative procedure, considering utility of a multistep precautionary measure and the weight of these measures on post-operative stay of patients, may be an arm for control really post-operative infectious complications, according with control of sterilization's procedures and diffusion of dedicated device.


Subject(s)
Antibiotic Prophylaxis , Bacterial Infections/prevention & control , Intraoperative Care , Postoperative Complications/prevention & control , Humans , Surgical Wound Infection/prevention & control
12.
Biochem Cell Biol ; 80(4): 475-82, 2002.
Article in English | MEDLINE | ID: mdl-12234101

ABSTRACT

The aetiology of neuroblastoma remains obscure, although a number of neuropeptides have been implicated in its pathogenesis. Using the mouse neuroblastoma cell line Neuro2a as a model, we have investigated the mitogenic actions of prolactin (PRL) and two hypothalamo-pituitary-adrenal stress axis hormones, corticotropin-releasing factor (CRF) and corticosterone. Using established polyclonal PRL receptor antisera with immunofluorescence cytochemistry, we show that the Neuro2a cells possess immunoreactive forms of both the long and short forms of the receptor. PRL and CRF were effective as mitogens in Neuro2a cell cultures, where a 10(-7) M concentration of PRL or CRF elicited a two-fold increase in the numbers of cells after 72 h (p < 0.0001). Corticosterone, however, attenuated their proliferation. These data suggest that prolactin may act to increase the proliferation and regulation of neuroblastomas and that the effects of PRL may be modified by hypothalamo-pituitary-adrenal hormones.


Subject(s)
Corticosterone/metabolism , Corticotropin-Releasing Hormone/metabolism , Neuroblastoma/metabolism , Prolactin/metabolism , Receptors, Prolactin/genetics , Animals , Base Sequence , Cell Division/physiology , Mice , Microscopy, Confocal , Molecular Sequence Data , Neuroblastoma/immunology , RNA, Messenger , Receptors, Prolactin/biosynthesis , Receptors, Prolactin/immunology
13.
J Exp Anal Behav ; 75(3): 357-61; discussion 367-78, 2001 May.
Article in English | MEDLINE | ID: mdl-11453628

ABSTRACT

Two-factor theory remains a viable account of avoidance behavior. By emphasizing the interplay of respondent and operant contingencies, two-factor theory encourages the analysis of stimuli that mediate molar consequences and incorporates control by local events as well as events that are temporally remote, improbable, or cumulative.


Subject(s)
Appetitive Behavior , Avoidance Learning , Motivation , Animals , Conditioning, Operant , Electroshock , Humans , Psychological Theory
14.
Endocrinology ; 141(9): 3493-505, 2000 Sep.
Article in English | MEDLINE | ID: mdl-10965923

ABSTRACT

The use of pituitary cell type-specific promoters is a powerful molecular tool to achieve pituitary cell type-specific transcriptional targeting of transgenes encoded by viral vectors. It has recently been proposed that transcriptional targeting of therapeutic genes could be harnessed as a gene therapy strategy for the treatment of pituitary disease. We describe the successful use of the human PRL promoter (hPrl) encoded within recombinant adenovirus vectors to target transgene expression of Herpes Simplex Virus Type 1-Thymidine Kinase (HSV1-TK) or beta-galactosidase to lactotrophic cells in vitro and in vivo. Functionally, the restriction of expression of HSV1-TK to lactotrophic tumor cells, using the hPrl promoter, resulted in the cell type-specific induction of apoptosis in the lactotrophic GH3 tumor cell line, in the presence of ganciclovir (GCV). In the corticotrophic AtT20 cell line, we detected neither HSV1-TK expression, nor apoptosis in the presence of GCV. The hPrl promoter encoded within a recombinant adenoviral vector also restricted transgene expression to lactotrophic cells in primary anterior pituitary (AP) cultures, and importantly, within the anterior pituitary gland in vivo. When the HSV1-TK driven by hPrl promoter was used in an in vivo model ofestrogen/sulpiride lactotroph induced hyperplasia within the AP in situ, the treatment was not effective in either reducing the weight of the gland, the number of lactotrophic cells within the transduced area in vivo, or the circulating PRL levels. This is in contrast to the human cytomegalovirus promoter (hCMV) driving expression of HSV1-TK in the same experimental paradigm, which was effective in reducing pituitary weight and circulating PRL levels. Our results have important implications in the design of gene therapy strategies for pituitary tumors. We demonstrate that both the choice of the in vivo animal model, i.e. adenoma in the AP gland in situ, and the particular gene therapy strategy chosen, i.e. use of strong ubiquitous promoters vs. weaker but cell type-specific promoters, determine the experimental therapeutic outcome.


Subject(s)
Adenoviridae/genetics , Antipsychotic Agents/pharmacology , Estrogens/pharmacology , Gene Targeting/methods , Genetic Vectors/genetics , Pituitary Gland, Anterior/cytology , Sulpiride/pharmacology , Transcription, Genetic/genetics , Animals , Apoptosis/drug effects , Cell Line , Galactosidases/genetics , Herpesvirus 1, Human/enzymology , Hyperplasia/chemically induced , Hyperplasia/pathology , Immunohistochemistry , Indicators and Reagents , Pituitary Gland, Anterior/pathology , Pituitary Hormones, Anterior/blood , Rats , Rats, Inbred BUF , Transgenes/genetics
15.
J Clin Endocrinol Metab ; 85(3): 1296-305, 2000 Mar.
Article in English | MEDLINE | ID: mdl-10720079

ABSTRACT

We tested the hypothesis that gene transfer using recombinant adenovirus vectors (RAds) expressing herpes simplex virus type 1 thymidine kinase (HSV1-TK) might offer an alternative therapeutic approach for the treatment of pituitary prolactinomas that do not respond to classical treatment strategies. HSV1-TK converts the prodrug ganciclovir (GCV) to GCV monophosphate, which is in turn further phosphorylated by cellular kinases to GCV triphosphate, which is toxic to proliferating cells. One attractive feature of this system is the bystander effect, whereby untransduced cells are also killed. Our results show that RAd/HSV1-TK in the presence of GCV is nontoxic for the normal anterior pituitary (AP) gland in vitro, but causes cell death in the pituitary tumor cell lines GH3, a PRL/GH-secreting cell line, and AtT20, a corticotrophic cell line. We have used sulpiride- and oestrogen-induced lactotroph hyperplasia within the rat AP gland as an in vivo animal model. Intrapituitary infection of rats bearing oestrogen-induced lactotroph hyperplasia, with RAd/ HSV1-TK and subsequent treatment with GCV, decreases plasma PRL levels and reduces the mass of the pituitary gland. More so, there were no deleterious effects on circulating levels of other AP hormones, suggesting that the treatment was nontoxic to the AP gland in situ. In summary, our results show that suicide gene therapy using the HSV1-TK transgene could be further developed as a useful treatment to complement current therapies for prolactinomas.


Subject(s)
Adenoviridae/genetics , Estrogens/pharmacology , Genetic Therapy , Herpesvirus 1, Human/genetics , Pituitary Neoplasms/therapy , Prolactinoma/therapy , Thymidine Kinase/genetics , Animals , Apoptosis/genetics , Cell Line , Fluorescent Antibody Technique , Herpesvirus 1, Human/enzymology , Immunohistochemistry , Male , Pituitary Gland, Anterior/virology , Rats , Tumor Cells, Cultured
17.
Behav Anal ; 22(2): 109-16, 1999.
Article in English | MEDLINE | ID: mdl-22478328

ABSTRACT

Statistical inference promises automatic, objective, reliable assessments of data, independent of the skills or biases of the investigator, whereas the single-subject methods favored by behavior analysts often are said to rely too much on the investigator's subjective impressions, particularly in the visual analysis of data. In fact, conventional statistical methods are difficult to apply correctly, even by experts, and the underlying logic of null-hypothesis testing has drawn criticism since its inception. By comparison, single-subject methods foster direct, continuous interaction between investigator and subject and development of strong forms of experimental control that obviate the need for statistical inference. Treatment effects are demonstrated in experimental designs that incorporate replication within and between subjects, and the visual analysis of data is adequate when integrated into such designs. Thus, single-subject methods are ideal for shaping-and maintaining-the kind of experimental practices that will ensure the continued success of behavior analysis.

18.
Neuroreport ; 9(14): 3135-40, 1998 Oct 05.
Article in English | MEDLINE | ID: mdl-9831440

ABSTRACT

The existence of a CRF-dependent inhibition of GnRH transcription was investigated using a neuronal GnRH-expressing cell line (Gn11) stably transfected with mouse (-611 bp) or chicken (-3000 bp) GnRH promoter/luciferase reporter constructs. The presence of the CRF-R1 receptor was established using a specific CRF-R1 antiserum. After 7 h of incubation, urotensin-I and sauvagine increased the mouse GnRH-reporter bioluminescence by 1.3- and 1.2-fold, respectively, compared with control cells. Subsequently, CRF, urotensin-I and sauvagine decreased luciferase reporter activity to about 60% of the control values after 14 h. Similar trends occurred with the chicken GnRH promoter with UI increasing reporter gene activity 2.4-fold over the controls after 14 h incubation. These data provide additional evidence for the direct regulation of GnRH transcription by CRF-like peptides.


Subject(s)
Corticotropin-Releasing Hormone/genetics , Gonadotropin-Releasing Hormone/genetics , Neurons/physiology , Transcription, Genetic/physiology , Urotensins/genetics , Amphibian Proteins , Animals , Cell Line, Transformed , Gene Expression/drug effects , Gene Expression/physiology , Genes, Reporter , Luciferases , Mice , Molecular Sequence Data , Neurons/chemistry , Neuropeptides/genetics , Peptide Hormones , Peptides/pharmacology , Promoter Regions, Genetic/physiology , Sequence Homology, Amino Acid , Stress, Physiological/physiopathology , Transfection , Vasodilator Agents/pharmacology
19.
Mol Cell Endocrinol ; 142(1-2): 191-202, 1998 Jul 25.
Article in English | MEDLINE | ID: mdl-9783915

ABSTRACT

Procorticotrophin-releasing hormone (proCRH) is expressed mainly in the hypothalamus and in the placenta, where it undergoes tissue-specific endoproteolysis. Our results show that within stably transfected AtT20/D16V cells proCRH is cleaved to generate two fragments of approximately 8 and 3 kDa which could account for proCRH(125-194) and proCRH(125-151), respectively, and a 4.5 kDa product which could account for mature IR-CRH(1-41). The immunofluorescence staining patterns for IR-CRH and IR-ACTH and their response of secretagogues indicate targeting of proCRH and POMC to the secretory pathway in transfected AtT20 cells. In this work, we have used a unique set of specific RIAs and IRMAs to the full length POMC and proCRH molecules and several products of endoproteolytic processing to assess if they could be released differentially in response to stimulation. Although the release of both IR-ACTH and IR-CRH peptides from transfected AtT20 cells is stimulated in response to exposure to high potassium stimulation (51 mM KCl/SmM CaCl2), the sorting index (SI) suggests that mature ACTH is sorted to the regulated secretory pathway 2.1-fold more efficiently than mature CRH(1-41). Mature ACTH is also sorted to the regulated secretory pathway 9-fold more efficiently than IR-proCRH(125-151). Also, mature CRH(1-41) is sorted to the regulated secretory pathway 3-fold more efficiently than IR-proCRH(125-151). These results therefore indicate that the intracellular mechanisms for the storage and release of POMC, proCRH and their endoproteolytic products differ and would sustain the hypothesis that within mammalian peptidergic cells, different biologically active peptides originating from the same or different precursor molecules, could be differentially released in response to specific stimuli. This would give these cells the capacity to finely regulate neurotransmitter release in response to environmental and physiological demands.


Subject(s)
Corticotropin-Releasing Hormone/metabolism , Endopeptidases/metabolism , Protein Precursors/metabolism , Adrenocorticotropic Hormone/analysis , Adrenocorticotropic Hormone/metabolism , Calcium/pharmacology , Cell Line , Chromatography, Gel , Chromatography, High Pressure Liquid , Corticotropin-Releasing Hormone/analysis , Corticotropin-Releasing Hormone/genetics , Fluorescent Antibody Technique , Humans , Iodine Radioisotopes , Peptide Fragments/metabolism , Potassium/pharmacology , Protein Precursors/genetics , Radioimmunoassay , Transfection
20.
J Histochem Cytochem ; 46(10): 1193-7, 1998 Oct.
Article in English | MEDLINE | ID: mdl-9742076

ABSTRACT

We investigated the intracellular localization of CRH in transiently transfected COS-7 cells expressing the full-length rat corticotropin-releasing hormone (CRH) precursor cDNA. CRH synthesized by transfected COS-7 cells is mainly stored intracellularly. In contrast, CHO-K1 cells expressing the same CRH precursor stored and released equal amounts of immunoreactive (IR)-CRH. Ultrastructural analysis revealed that CRH is stored in electron-dense aggregates in the RER of transiently transfected COS-7 cells and does not migrate into the Golgi apparatus. On the basis of the different intracellular localization, storage, and release of CRH in COS-7 and CHO-K1 cells, we hypothesize that the intracellular trafficking of CRH within the constitutive secretory pathway for protein secretion not only depends on its primary amino acid sequence but might also be influenced by intracellular conditions or factors.


Subject(s)
COS Cells/metabolism , Corticotropin-Releasing Hormone/metabolism , Animals , CHO Cells , COS Cells/ultrastructure , Cricetinae , Endoplasmic Reticulum, Rough/metabolism , Golgi Apparatus/metabolism , Microscopy, Electron , Rats , Transfection
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