Abstract The relationships between adrenocorticotrophin (ACTH) content, basal ACTH secretion and the ACTH-secretory response to corticotrophin-releasing factor (CRF) or vasopressin in cultured rat anterior pituitary cells were examined in studies using chloroquine, an agent that diverts nascent ACTH from a storage pathway to direct release from cells. Chloroquine (200 mUM from t=minus 2 h) significantly elevated the basal ACTH secretory rate (by 0.7 +/- 0.2 ng over 30 min incubation, 1.1 +/- 0.3 ng over 60 min and 2.3 +/- 0.6 ng over 120 min). It also decreased the ACTH-secretory response to CRF (2.9+/-0.5 vs 4.6 +/- 0.5 ng/well over 30 min; 4.3 +/- 0.7 vs 8.0 +/- 1.4 ng/well over 60 min; 12.4+/-1.7 vs 20.2 +/- 3.6 ng/well over 120 min). In marked contrast, the net responses to vasopressin were unaltered (0.9 +/- 0.3 vs 0.9+/-0.2 ng/well over 30 min; 2.2 +/- 0.9 vs 2.1 +/-0.3 ng/well over 60 min; 3.8+/-0.9 vs 3.3 +/- 1.0 ng/well over 120 min). These data further support the association of the ACTH-secretory response to CRF with stored cellular ACTH, and the minimal dependence of the response to vasopressin on stored ACTH.
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Nanomaterials (Basel)
July 2024
Pulmonary Pathogenesis and Immunotoxicology Laboratory, Department of Environmental and Public Health Sciences, University of Cincinnati College of Medicine, Cincinnati, OH 45267, USA.
There is a need for the assessment of respiratory hazard potential and mode of action of carbon nanotubes (CNTs) before their approval for technological or medical applications. In CNT-exposed lungs, both alveolar macrophages (MФs), which phagocytose CNTs, and alveolar epithelial type II cells (AECII cells), which show tissue injury, are impacted but cell-cell interactions between them and the impacted mechanisms are unclear. To investigate this, we first optimized an air-liquid interface (ALI) transwell coculture of human AECII cell line A549 (upper chamber) and human monocyte cell line THP-1 derived macrophages (lower chamber) in a 12-well culture by exposing macrophages to CNTs at varying doses (5-60 ng/well) for 12-48 h and measuring the epithelial response markers for cell differentiation/maturation (proSP-C), proliferation (Ki-67), and inflammation (IL-1β).
View Article and Find Full Text PDFPoult Sci
November 2023
Department of Pathobiology, Pharmacology and Zoological Medicine, Faculty of Veterinary Medicine, Ghent University, 9820 Merelbeke, Belgium.
In order to minimize animal loss and economical loss, industrial poultry is heavily vaccinated against infectious agents. mRNA vaccination is an effective vaccination platform, yet little to no comprehensive, comparative studies in avians can be found. Nevertheless, poultry mRNA vaccination could prove to be very interesting due to the relatively low production cost, especially true when using self-amplifying mRNA (saRNA), and their extreme adaptability to new pathogens.
View Article and Find Full Text PDFAnim Biotechnol
December 2023
College of Animal Science and Technology, Shihezi University, Shihezi, Xinjiang, P. R. China.
In this study, we recombinantly expressed the V protein of the peste des petits ruminants virus (PPRV) and evaluated its diagnostic value for PPRV infection using an indirect ELISA (i-ELISA). The optimal concentration of the coated antigen of V protein was 15 ng/well at a serum dilution of 1:400, and the optimal positive threshold value was 0.233.
View Article and Find Full Text PDFVaccines (Basel)
March 2023
Institute of Veterinary Medicine, Jiangsu Academy of Agricultural Science, Nanjing 210014, China.
Goose astrovirus (GAstV) was classified into GAstV-1 and GAstV-2, and both caused gosling viral gout. Recently, there has been no effective commercial vaccine to control the infection. It is important to establish serological methods to distinguish between the two genotypes.
View Article and Find Full Text PDFJ Biol Chem
December 2022
Department of Preventive Veterinary Medicine, College of Veterinary Medicine, Northwest A&F University, Yangling, Shaanxi, China. Electronic address:
Circulation of influenza A virus (IAV), especially within poultry and pigs, continues to threaten public health. A simple and universal detecting method is important for monitoring IAV infection in different species. Recently, nanobodies, which show advantages of easy gene editing and low cost of production, are a promising novel diagnostic tool for the monitoring and control of global IAVs.
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