Moysés dos Santos Miranda, Fabiana Fernandes Bressan, Karina Gottardello Zecchin, Anibal Eugênio Vercesi, Ligia Garcia Mesquita, Giovana Krempel Fonseca Merighe, William Allan King, Otávio Mitio Ohashi, José Rodrigo Valim Pimentel, Felipe Perecin, Flávio Vieira Meirelles
{"title":"血清饥饿的凋亡成纤维细胞减少了囊胚的产生,但使牛在SCNT后发育到足月。","authors":"Moysés dos Santos Miranda, Fabiana Fernandes Bressan, Karina Gottardello Zecchin, Anibal Eugênio Vercesi, Ligia Garcia Mesquita, Giovana Krempel Fonseca Merighe, William Allan King, Otávio Mitio Ohashi, José Rodrigo Valim Pimentel, Felipe Perecin, Flávio Vieira Meirelles","doi":"10.1089/clo.2009.0028","DOIUrl":null,"url":null,"abstract":"<p><p>Cell cycle synchronization by serum starvation (SS) induces apoptosis in somatic cells. This side effect of SS is hypothesized to negatively affect the outcome of somatic cell nuclear transfer (SCNT). We determined whether apoptotic fibroblasts affect SCNT yields. Serum-starved, adult, bovine fibroblasts were stained with annexin V-FITC/propidium iodide to allow apoptosis detection by flow cytometry. Positive and negative cells sorted by fluorescence activated cell sorting (FACS) and an unsorted control group were used as nuclear donors for SCNT. Reconstructed embryos were cultured in vitro and transferred to synchronized recipients. Apoptosis had no effect on fusion and cleavage rates; however, it resulted in reductions in blastocyst production and quality measured by apoptotic index. However, reconstructed embryos with apoptotic cells resulted in pregnancy rates similar to that of the control on day 30, and generated one live female calf. In conclusion, we showed that apoptotic cells present in serum-starved cultures negatively affect embryo production after SCNT without compromising full-term development. Further studies will evaluate the ability of the oocyte to reprogram cells in specific phases of apoptosis.</p>","PeriodicalId":49217,"journal":{"name":"Cloning Stem Cells","volume":" ","pages":"565-73"},"PeriodicalIF":0.0000,"publicationDate":"2009-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1089/clo.2009.0028","citationCount":"27","resultStr":"{\"title\":\"Serum-starved apoptotic fibroblasts reduce blastocyst production but enable development to term after SCNT in cattle.\",\"authors\":\"Moysés dos Santos Miranda, Fabiana Fernandes Bressan, Karina Gottardello Zecchin, Anibal Eugênio Vercesi, Ligia Garcia Mesquita, Giovana Krempel Fonseca Merighe, William Allan King, Otávio Mitio Ohashi, José Rodrigo Valim Pimentel, Felipe Perecin, Flávio Vieira Meirelles\",\"doi\":\"10.1089/clo.2009.0028\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Cell cycle synchronization by serum starvation (SS) induces apoptosis in somatic cells. This side effect of SS is hypothesized to negatively affect the outcome of somatic cell nuclear transfer (SCNT). We determined whether apoptotic fibroblasts affect SCNT yields. Serum-starved, adult, bovine fibroblasts were stained with annexin V-FITC/propidium iodide to allow apoptosis detection by flow cytometry. Positive and negative cells sorted by fluorescence activated cell sorting (FACS) and an unsorted control group were used as nuclear donors for SCNT. Reconstructed embryos were cultured in vitro and transferred to synchronized recipients. Apoptosis had no effect on fusion and cleavage rates; however, it resulted in reductions in blastocyst production and quality measured by apoptotic index. However, reconstructed embryos with apoptotic cells resulted in pregnancy rates similar to that of the control on day 30, and generated one live female calf. In conclusion, we showed that apoptotic cells present in serum-starved cultures negatively affect embryo production after SCNT without compromising full-term development. Further studies will evaluate the ability of the oocyte to reprogram cells in specific phases of apoptosis.</p>\",\"PeriodicalId\":49217,\"journal\":{\"name\":\"Cloning Stem Cells\",\"volume\":\" \",\"pages\":\"565-73\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2009-12-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1089/clo.2009.0028\",\"citationCount\":\"27\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Cloning Stem Cells\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1089/clo.2009.0028\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cloning Stem Cells","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1089/clo.2009.0028","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Serum-starved apoptotic fibroblasts reduce blastocyst production but enable development to term after SCNT in cattle.
Cell cycle synchronization by serum starvation (SS) induces apoptosis in somatic cells. This side effect of SS is hypothesized to negatively affect the outcome of somatic cell nuclear transfer (SCNT). We determined whether apoptotic fibroblasts affect SCNT yields. Serum-starved, adult, bovine fibroblasts were stained with annexin V-FITC/propidium iodide to allow apoptosis detection by flow cytometry. Positive and negative cells sorted by fluorescence activated cell sorting (FACS) and an unsorted control group were used as nuclear donors for SCNT. Reconstructed embryos were cultured in vitro and transferred to synchronized recipients. Apoptosis had no effect on fusion and cleavage rates; however, it resulted in reductions in blastocyst production and quality measured by apoptotic index. However, reconstructed embryos with apoptotic cells resulted in pregnancy rates similar to that of the control on day 30, and generated one live female calf. In conclusion, we showed that apoptotic cells present in serum-starved cultures negatively affect embryo production after SCNT without compromising full-term development. Further studies will evaluate the ability of the oocyte to reprogram cells in specific phases of apoptosis.