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Originally discovered through mutations in Drosophila more than 100 yr ago, and with the first Notch gene cloned more than 30 yr ago, we are still gaining new insights into the broad effects of Notch signaling in organisms across the metazoan spectrum and its requirement for normal development of most organs in the body. In this review, we provide an overview of the Notch signaling mechanism at the molecular level and discuss how the pathway, which is architecturally quite simple, is able to engage in the control of cell fates in a broad variety of cell types. We discuss the current understanding of how Notch signaling can become derailed, either by direct mutations or by aberrant regulation, and the expanding spectrum of diseases and cancers that is a consequence of Notch dysregulation. 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Subfamilies found in invertebrates or mammals are functionally distinct. The degenerins in Caenorhabditis elegansparticipate in mechanotransduction in neuronal cells, FaNaC in snails is a ligand-gated channel activated by neuropeptides, and the Drosophila subfamily is expressed in gonads and neurons. In mammals, ENaC mediates Na\u003Cjats:sup>+\u003C\u002Fjats:sup>transport in epithelia and is essential for sodium homeostasis. The ASIC genes encode proton-gated cation channels in both the central and peripheral nervous system that could be involved in pain transduction. This review summarizes the physiological roles of the different channels belonging to this family, their biophysical and pharmacological characteristics, and the emerging knowledge of their molecular structure. Although functionally different, the ENaC\u002FDEG family members share functional domains that are involved in the control of channel activity and in the formation of the pore. 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The corpus luteum develops from residual follicular granulosal and thecal cells after ovulation. Luteinizing hormone (LH) from the anterior pituitary is important for normal development and function of the corpus luteum in most mammals, although growth hormone, prolactin, and estradiol also play a role in several species. The mature corpus luteum is composed of at least two steroidogenic cell types based on morphological and biochemical criteria and on the follicular source of origin. Small luteal cells appear to be of thecal cell origin and respond to LH with increased secretion of progesterone. LH directly stimulates the secretion of progesterone from small luteal cells via activation of the protein kinase A second messenger pathway. Large luteal cells are of granulosal cell origin and contain receptors for PGF\u003Cjats:sub>2α\u003C\u002Fjats:sub>and appear to mediate the luteolytic actions of this hormone. If pregnancy does not occur, the corpus luteum must regress to allow follicular growth and ovulation and the reproductive cycle begins again. Luteal regression is initiated by PGF\u003Cjats:sub>2α\u003C\u002Fjats:sub>of uterine origin in most subprimate species. The role played by PGF\u003Cjats:sub>2α\u003C\u002Fjats:sub>in primates remains controversial. In primates, if PGF\u003Cjats:sub>2α\u003C\u002Fjats:sub>plays a role in luteolysis, it appears to be of ovarian origin. The antisteroidogenic effects of PGF\u003Cjats:sub>2α\u003C\u002Fjats:sub>appear to be mediated by the protein kinase C second messenger pathway, whereas loss of luteal cells appears to follow an influx of calcium, activation of endonucleases, and an apoptotic form of cell death. If the female becomes pregnant, continued secretion of progesterone from the corpus luteum is required to provide an appropriate uterine environment for maintenance of pregnancy. 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Fertil., 52, 19",{},{"id":24,"text":10961,"url":24,"identifiers":10962},"10.1016\u002FS0039-128X(98)00037-3",{"doi":10961},{"id":24,"text":10964,"url":24,"identifiers":10965},"10.1038\u002F284555a0",{"doi":10964},{"id":24,"text":10967,"url":24,"identifiers":10968},"10.1152\u002Fphysrev.1994.74.1.139",{"doi":10967},{"id":24,"text":10970,"url":24,"identifiers":10971},"10.2527\u002F1993.712481x",{"doi":10970},{"id":24,"text":10973,"url":24,"identifiers":10974},"10.1096\u002Ffasebj.7.10.8344485",{"doi":10973},{"id":24,"text":10976,"url":24,"identifiers":10977},"10.1095\u002Fbiolreprod51.4.623",{"doi":10976},{"id":24,"text":10979,"url":24,"identifiers":10980},"10.1006\u002Fbbrc.1997.6833",{"doi":10979},{"id":10982,"createTime":10983,"updateTime":10983,"relativeEntities":10984,"slug":10985,"properties":10986,"entityType":149,"verifyStatus":150,"verifyTime":11000,"verifyNote":151,"syncStatus":23,"languages":11001,"translateLanguages":24,"viewCount":25,"primaryUrl":11002,"fullTextUrl":24,"authors":11003,"publicationType":668,"publisherRelationship":11023,"citationCount":11054,"citationInfo":11055,"publishDate":9788,"publishYear":9789,"citationAnalyzeStatus":23,"lastCitationAnalyze":24,"indexDatabases":24,"openAccess":24,"references":11061,"isForceReanalyzing":2997},"eb6c0775-4f32-4f9c-93f9-060193803c37","2024-09-02T23:31:18.021+00:00",[],"Oxysterols-Modulators-of-Cholesterol-Metabolism-and-Other-Processes",{"mag":10987,"keywords":10989,"openalex":10990,"abstract":10992,"title":10994,"pm":10996,"doi":10998},{"VOID":10988},"1862564406",{},{"VOID":10991},"W1862564406",{"EN":10993},"\u003Cjats:p>Oxygenated derivatives of cholesterol (oxysterols) present a remarkably diverse profile of biological activities, including effects on sphingolipid metabolism, platelet aggregation, apoptosis, and protein prenylation. The most notable oxysterol activities center around the regulation of cholesterol homeostasis, which appears to be controlled in part by a complex series of interactions of oxysterol ligands with various receptors, such as the oxysterol binding protein, the cellular nucleic acid binding protein, the sterol regulatory element binding protein, the LXR nuclear orphan receptors, and the low-density lipoprotein receptor. Identification of the endogenous oxysterol ligands and elucidation of their enzymatic origins are topics of active investigation. Except for 24,25-epoxysterols, most oxysterols arise from cholesterol by autoxidation or by specific microsomal or mitochondrial oxidations, usually involving cytochrome P-450 species. Oxysterols are variously metabolized to esters, bile acids, steroid hormones, cholesterol, or other sterols through pathways that may differ according to the type of cell and mode of experimentation (in vitro, in vivo, cell culture). Reliable measurements of oxysterol levels and activities are hampered by low physiological concentrations (∼0.01–0.1 μM in plasma) relative to cholesterol (∼5,000 μM) and by the susceptibility of cholesterol to autoxidation, which produces artifactual oxysterols that may also have potent activities. Reports describing the occurrence and levels of oxysterols in plasma, low-density lipoproteins, various tissues, and food products include many unrealistic data resulting from inattention to autoxidation and to limitations of the analytical methodology. Because of the widespread lack of appreciation for the technical difficulties involved in oxysterol research, a rigorous evaluation of the chromatographic and spectroscopic methods used in the isolation, characterization, and quantitation of oxysterols has been included. This review comprises a detailed and critical assessment of current knowledge regarding the formation, occurrence, metabolism, regulatory properties, and other activities of oxysterols in mammalian systems.\u003C\u002Fjats:p>",{"EN":10995},"Oxysterols: Modulators of Cholesterol Metabolism and Other Processes",{"VOID":10997},"10617772",{"VOID":10999},"10.1152\u002Fphysrev.2000.80.1.361","2024-09-02T23:31:18.020+00:00",[153],"https:\u002F\u002Fwww.physiology.org\u002Fdoi\u002F10.1152\u002Fphysrev.2000.80.1.361",[11004],{"id":11005,"sortIndex":25,"researcher":24,"roles":11006,"affiliations":11007,"properties":11018},"a8a7010a-e065-4f44-89df-59b80f5bbb20",[],[11008],{"id":11009,"sortIndex":25,"affiliation":11010,"properties":24},"ecc1c919-2f92-4bc9-a183-ce140e837903",{"id":11011,"createTime":11012,"updateTime":11012,"relativeEntities":11013,"slug":11014,"properties":11015,"entityType":69,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":25},"9503adcf-05d0-463b-b771-98f47638ceed","2024-09-02T23:31:18.038+00:00",[],"Departments-of-Biochemistry-and-Cell-Biology-and-of-Chemistry-Rice-University-Houston-Texas",{"title":11016},{"EN":11017},"Departments of Biochemistry and Cell Biology and of Chemistry, Rice University, Houston, Texas",{"openalex":11019,"title":11021},{"VOID":11020},"A5062314199",{"EN":11022},"George J. 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