Mechanical stimulation by osmotic and hydrostatic pressure activates Drosophila oocytes in vitro in a calcium-dependent manner
Embryogenesis in vertebrates and marine invertebrates begins when a mature oocyte is fertilized, resulting in a rise in intracellular calcium (Ca2+) that activates development. Insect eggs activate without fertilization via an unknown signal imparted to the egg during ovulation or egg laying. One hy...
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description | Embryogenesis in vertebrates and marine invertebrates begins when a mature oocyte is fertilized, resulting in a rise in intracellular calcium (Ca2+) that activates development. Insect eggs activate without fertilization via an unknown signal imparted to the egg during ovulation or egg laying. One hypothesis for the activating signal is that deformation of eggs as they pass through a tight orifice provides a mechanical stimulus to trigger activation. Ovulation could produce two forms of mechanical stimulus: external pressure resulting from the passage of oocytes from the ovary into the narrow oviducts, and osmotic pressure caused by hydration-induced swelling of the oocyte within the oviducts. Ovulation could also trigger activation by placing the oocyte in a new environment that contains an activating substance, such as a particular ion. Here, we provide the first evidence that Drosophila oocytes require Ca2+ for activation, and that activation can be triggered in vitro by mechanical stimuli, specifically osmotic and hydrostatic pressure. Our results suggest that activation in Drosophila is triggered by a mechanosensitive process that allows external Ca2+ to enter the oocyte and drive the events of activation. This will allow exploitation of Drosophila genetics to dissect molecular pathways involving Ca2+ and the activation of development. |
doi_str_mv | 10.1016/j.ydbio.2008.01.014 |
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Our results suggest that activation in Drosophila is triggered by a mechanosensitive process that allows external Ca2+ to enter the oocyte and drive the events of activation. 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Insect eggs activate without fertilization via an unknown signal imparted to the egg during ovulation or egg laying. One hypothesis for the activating signal is that deformation of eggs as they pass through a tight orifice provides a mechanical stimulus to trigger activation. Ovulation could produce two forms of mechanical stimulus: external pressure resulting from the passage of oocytes from the ovary into the narrow oviducts, and osmotic pressure caused by hydration-induced swelling of the oocyte within the oviducts. Ovulation could also trigger activation by placing the oocyte in a new environment that contains an activating substance, such as a particular ion. Here, we provide the first evidence that Drosophila oocytes require Ca2+ for activation, and that activation can be triggered in vitro by mechanical stimuli, specifically osmotic and hydrostatic pressure. Our results suggest that activation in Drosophila is triggered by a mechanosensitive process that allows external Ca2+ to enter the oocyte and drive the events of activation. This will allow exploitation of Drosophila genetics to dissect molecular pathways involving Ca2+ and the activation of development.</description><subject>Animals</subject><subject>Calcium</subject><subject>Calcium - metabolism</subject><subject>Drosophila</subject><subject>Drosophila melanogaster - growth & development</subject><subject>Drosophila melanogaster - metabolism</subject><subject>Egg activation</subject><subject>Female</subject><subject>French press</subject><subject>Gadolinium</subject><subject>Gadolinium - pharmacology</subject><subject>Hydrostatic Pressure</subject><subject>Mechanosensation</subject><subject>Meiosis</subject><subject>Oocytes - drug effects</subject><subject>Oocytes - growth & development</subject><subject>Oocytes - metabolism</subject><subject>Osmosis</subject><subject>Pressure</subject><subject>Protein Biosynthesis</subject><subject>Stress, Mechanical</subject><subject>Transient Receptor Potential Channels - metabolism</subject><subject>Vitelline Membrane - drug effects</subject><subject>Vitelline Membrane - growth & development</subject><subject>Vitelline Membrane - metabolism</subject><issn>0012-1606</issn><issn>1095-564X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUcuqFDEQDaJ4x6tfIEhW7nqsPPq1UJDrE664UXAX0ulqJ0N30ibpgd747aadwcdGoYqkUqdOquoQ8pjBngGrnh33a99Zv-cAzR5YNnmH7Bi0ZVFW8stdsgNgvGAVVFfkQYxHABBNI-6TK9YIkCWXO_L9A5qDdtbokcZkp2XUyXpHu5X6OPlkDdWup4e1Dz4mvcVzwBiXgFSbZE86YaSvctLPBztq6r1Ztyfr6Mmm4LeLppne2GUqepzR9egSnbRzGB6Se4MeIz66nNfk85vXn27eFbcf376_eXlbmLKUqdCC86oDrQF5h8CMaXqevaoE1g03UJumHbDFGss8JNftoM3QZnQzyNYwcU1enHnnpZuwN7mDoEc1BzvpsCqvrfo74-xBffUnxUXNWVVmgqcXguC_LRiTmmw0OI7aoV-iqkGKWkj4L5AzkLVsN0ZxBpq8vBhw-NUNA7UJrI7qp8BqE1gByyZz1ZM_B_ldc1E0A56fAZjXebIYVDQWncHeBjRJ9d7-84Mffaa8-g</recordid><startdate>20080401</startdate><enddate>20080401</enddate><creator>Horner, Vanessa L.</creator><creator>Wolfner, Mariana F.</creator><general>Elsevier Inc</general><scope>6I.</scope><scope>AAFTH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7SS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20080401</creationdate><title>Mechanical stimulation by osmotic and hydrostatic pressure activates Drosophila oocytes in vitro in a calcium-dependent manner</title><author>Horner, Vanessa L. ; Wolfner, Mariana F.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c554t-a3226b0aa0e2be01cc8d2c8d663e782c07c89fe9e7e50032a9facf90e28f49c13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Animals</topic><topic>Calcium</topic><topic>Calcium - metabolism</topic><topic>Drosophila</topic><topic>Drosophila melanogaster - growth & development</topic><topic>Drosophila melanogaster - metabolism</topic><topic>Egg activation</topic><topic>Female</topic><topic>French press</topic><topic>Gadolinium</topic><topic>Gadolinium - pharmacology</topic><topic>Hydrostatic Pressure</topic><topic>Mechanosensation</topic><topic>Meiosis</topic><topic>Oocytes - drug effects</topic><topic>Oocytes - growth & development</topic><topic>Oocytes - metabolism</topic><topic>Osmosis</topic><topic>Pressure</topic><topic>Protein Biosynthesis</topic><topic>Stress, Mechanical</topic><topic>Transient Receptor Potential Channels - metabolism</topic><topic>Vitelline Membrane - drug effects</topic><topic>Vitelline Membrane - growth & development</topic><topic>Vitelline Membrane - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Horner, Vanessa L.</creatorcontrib><creatorcontrib>Wolfner, Mariana F.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Developmental biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Horner, Vanessa L.</au><au>Wolfner, Mariana F.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mechanical stimulation by osmotic and hydrostatic pressure activates Drosophila oocytes in vitro in a calcium-dependent manner</atitle><jtitle>Developmental biology</jtitle><addtitle>Dev Biol</addtitle><date>2008-04-01</date><risdate>2008</risdate><volume>316</volume><issue>1</issue><spage>100</spage><epage>109</epage><pages>100-109</pages><issn>0012-1606</issn><eissn>1095-564X</eissn><abstract>Embryogenesis in vertebrates and marine invertebrates begins when a mature oocyte is fertilized, resulting in a rise in intracellular calcium (Ca2+) that activates development. Insect eggs activate without fertilization via an unknown signal imparted to the egg during ovulation or egg laying. One hypothesis for the activating signal is that deformation of eggs as they pass through a tight orifice provides a mechanical stimulus to trigger activation. Ovulation could produce two forms of mechanical stimulus: external pressure resulting from the passage of oocytes from the ovary into the narrow oviducts, and osmotic pressure caused by hydration-induced swelling of the oocyte within the oviducts. Ovulation could also trigger activation by placing the oocyte in a new environment that contains an activating substance, such as a particular ion. Here, we provide the first evidence that Drosophila oocytes require Ca2+ for activation, and that activation can be triggered in vitro by mechanical stimuli, specifically osmotic and hydrostatic pressure. Our results suggest that activation in Drosophila is triggered by a mechanosensitive process that allows external Ca2+ to enter the oocyte and drive the events of activation. This will allow exploitation of Drosophila genetics to dissect molecular pathways involving Ca2+ and the activation of development.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>18304524</pmid><doi>10.1016/j.ydbio.2008.01.014</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Calcium Calcium - metabolism Drosophila Drosophila melanogaster - growth & development Drosophila melanogaster - metabolism Egg activation Female French press Gadolinium Gadolinium - pharmacology Hydrostatic Pressure Mechanosensation Meiosis Oocytes - drug effects Oocytes - growth & development Oocytes - metabolism Osmosis Pressure Protein Biosynthesis Stress, Mechanical Transient Receptor Potential Channels - metabolism Vitelline Membrane - drug effects Vitelline Membrane - growth & development Vitelline Membrane - metabolism |
title | Mechanical stimulation by osmotic and hydrostatic pressure activates Drosophila oocytes in vitro in a calcium-dependent manner |
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