2013, Número 2
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Rev Mex Med Repro 2013; 5.6 (2)
Laboratorio de reproducción asistida
Neri VP, Carballo ME, Rocha CF, García VG, Acuña GMC, Uria GCE
Idioma: Español
Referencias bibliográficas: 96
Paginas: 104-127
Archivo PDF: 768.76 Kb.
FRAGMENTO
En los últimos años, los laboratorios de reproducción
asistida experimentaron notables cambios:
desde su entorno como parte importante de
una clínica de reproducción asistida hasta los
mínimos detalles que los componen y la disciplina con la
que los embriólogos se deben conducir en ellos.
REFERENCIAS (EN ESTE ARTÍCULO)
Alper M, Brinsden P, Fischer R, Wikland M. Is your IVF programme good? Hum Reprod 2002;17:8-10.
Gianaroli L, Plachot M, Van Kooij R, Al-Hasani S, et al. ESHRE guidelines for good practice in IVF laboratories.
Gardner D, Weissman A, Howles C, Shoham Z, et al. Textbook of assisted reproductive techniques. Laboratory and clinical perspectives. Edit. London. Cap. 1-2.
The Istanbul consensus workshop on embryo assessment: proceedings of an expert meeting Alpha Scientists in reproductive medicine and ESHRE Special Interest Group of Embryology Human Reproduction, 2011;26:1270-1283.
Karsu C, Caglar G, Vicdan K, Sozen E, et al. Smooth endoplasmic reticulum aggregations in all retrieved oocytes causing recurrent multiple anomalies: case report. Fertil Steril 2009;92:1496-1498.
Balakier H, Bouman D, Sojecki A, Librach C, et al. Morphological and cytogenetic analysis of human giant oocytes and giant embryos. Hum Reprod 2002;17:2394-2401.
Balaban B, Urman B, Isiklar A, Alatas C, et al. The effect of pronuclear morphology on embryo quality parameters and blastocyst transfer outcome. Hum Reprod 2001;16:2357-2361.
Antczak M, van Blerkom J. Temporal and spatial aspects of fragmentation in early human embryos: possible effects on developmental competence and association with the differential elimination of regulatory proteins from polarized domains. Hum Reprod 1999;14:429-447.
Balakier H, Cadesky K. The frequency and developmental capability of human embryos containing multinucleated blastomeres. Hum Reprod 1997;12:800-804.
Balaban B, Yakin K, Urman B. Randomized comparison of two different blastocyst grading systems. Fertil Steril 2006;85:559-563.
Braude P, Bolton V, Moore S. Human gene expression first occurs between the four -and eight- cell stages of preimplantation development. Nature 1988;333:459-461.
Cutting R, Morroll D, Roberts SA, Pickering S, et al. Elective single embryo transfer: guidelines for practice British Fertility Society and Association of Clinical Embryologists. Hum Fertil 2008;11:131-146.
Nanassy L, Carrell DT. Paternal effects on early embryogenesis. The J Clin Embryol 2008;11:9-28.
Editorial. Malformation risk in subfertile couples. Reprod BioMed Online 2012;25,225-226.
Frattarelli JL, Miller KA, Miller BT, Elkind-Hirsch K, et al. Male age negatively impacts embryo development and reproductive outcome in donor oocyte assisted reproductive technology cycles. Fertil Steril 2008;90:97-103.
Miller D, Brinkworth M, Iles D. Paternal DNA packaging in spermatozoa: more than the sum of its parts? DNA, histones, protamines and epigenetics. Reproduction 2010;139:287- 301.
Kobayashi H, Sato A, Otsu E, Hiura H, et al. Aberrant DNA methylation of imprinted loci in sperm from oligospermic patients. Hum Mol Genet 2007;16:2542-2551.
Emery BR, Carrell DT. The effect of epigenetic sperm abnormalities on early embryogenesis. Asian J Androl 2006;8:131-142.
Garrido N, García-Herrero S, Meseguer M. Assessment of sperm using ARNm microarray technology. Fertil Steril 2013;99:1008-1022.
WHO. Laboratory manual for the examination and processing of human semen. 5a ed. WHO Press, 2010.
Chavarro JE, Toth TL, Wright DL, Meeker JD, et al. Body mass index in relation to semen quality, sperm DNA integrity, and serum reproductive hormone levels among men attending an infertility clinic. Fertil Steril 2010;93:2222-2231.
De La Rochebrochard E, de Mouzon J, Thépot F, Thonneau P, French National IVF Registry (FIVNAT) association. Fathers over 40 and increased failure to conceive: the lessons of in vitro fertilization in France. Fertil Steril 2006;85:1420-1424.
Escudero T, Abdelhadi I, Sandalinas M, Munne S. Predictive value of sperm fluorescence in situ hybridization analysis on the outcome of preimplantation genetic diagnosis for translocations. Fertil Steril 2003;79:1528-1534.
Carballo ME, Roque A, Durán-Monterrosas LA, Kably AA. El valor de la edad paterna en los resultados de inseminación intrauterina. Ginecol Obstet Mex 2013;81:329-333.
O’Flynn KL, O’Brien BA, Varghese AC, Agarwal A. The genetic causes of male factor infertility: A review. Fertil Steril 2010;93:1-12.
Esteves SC, Agarwal A. Novel concepts in male infertility. Inter Braz J Urol 2011;37: 5-15.
Holstein AF, Schulze W, Davidoff M. Understanding spermatogenesis is a prerequisite for treatment. Reprod Biol Endocrinol 2003;1:107.
Sakkas D, Huszar. Paternal effects on reproductive outcome the clinical embryologist 2006;9:23-26.
Saunders CM, Larman MG, Parrington J, Cox LJ, et al. PLC: a sperm-specific trigger of Ca2+ oscillations in eggs and embryo. Development 2002;129:3533-3544.
Ugajin T, Terada Y, Hasegawa H, Nabeshima H, et al. The shape of the sperm midpiece in intracytoplasmic morphologically selected sperm injection relates sperm centrosomal function. J Assist Reprod Genet 2010; 27:75-81.
Wilson EB. The cell in development and inheritance. 2ª ed. New York: MacMillan, 1900;483.
Gilbert SF. Developmental biology. 10ª ed. USA: Sinauer Assoc, 2013;750.
Watson JD, Crick FH. Molecular structure of nucleic acids; a structure for deoxyribose nucleic acid. Nature 1953;171:737- 738.
International Human Genome Sequencing Consortium. Finishing the euchromatic sequence of the human genome. Nature 2004;431:931-945.
Recillas Targa F. La regulación de la cromatina, el switch en el encendido y apagado de genes. Comunicado Academia Mexicana de Ciencias 2013;28 Junio. Disponible en http://www.comunicacion.amc.edu.mx/comunicados/ la-regulacion-de-la-cromatina-el-switch-en-el-encendidoy- apagado-de-genes/
Babbitt GA. Chromatin evolving. American Scientist 2011;99:48-55.
Luque J, Herráez A. Texto ilustrado de biología molecular e ingeniería genética. Conceptos, técnicas y aplicaciones en ciencias de la salud. 1ª ed. Madrid: Elsevier, 2006;83-96.
Lemon B, Tjian R. Orchestrated response: a symphony of transcription factors for gene control. Genes Dev 2000;14:2551-2569.
Recillas Targa F, Zurita Ortega ME. Control de la expresión genética en eucariontes. En: Jiménez LF, Merchant H, editores. Biología celular y molecular. México: Prentice Hall, 2003;63-101.
Turner BM. Chromatin and gene regulation: Molecular mechanisms in epigenetics. Great Britain: Blackwell Science, 2001.
Cooper GM. La célula. 2ª ed. Madrid: Marbán, 2004;146-154.
Mattei MG, Lucini J. Heterochromatin, from chromosome to protein. Atlas of genetics and cytogenetics in oncology and heaematology. January 2003. Disponible en http://atlasgeneticsoncology. org//Deep/HeterochromatineDEEP.html
Smith K. Basic cytogenetic techniques: Culturing, slide making and G banding. En: Celis JE, editor. Cell biology. A laboratory handbook. Vol. 3. China: Elsevier Academic Press, 2006;381-386.
Contreras Bravo NC, Silva Aldana CT, Mateus Arbelaez HE. Citogenética aplicada a la medicina. Bogotá: Universidad del Rosario, 2009.
Warburton D, Kline J, Stein Z. Cytogenetic abnormalities in spontaneous abortions of recognized conceptions. In: Porter IH, Willey A, editors. Perinatal genetics: diagnosis and treatment. New York: Academic Press, 1986;133.
Hassold T, Hunt P. To err (meiotically) is human: the genesis of human aneuploidy. Nat Rev Genet 2001;2:280-291.
Lakovschek IC, Streubel B, Ulm B. Natural outcome of trisomy 13, trisomy 18, and triploidy after prenatal diagnosis. Am J Med Genet A 2011;155A:2626-2633.
López P, López R, Noriega L, Sepúlveda S. Diagnóstico genético preimplantacional: Análisis de aneuploidías únicas. An Fac Med 2013;74:11-14.
Acevedo-Gallegos S, García M, Benavides-Serralde A, Camargo-Marín L, et al. Association between selected structural defects and chromosomal abnormalities. Rev Invest Clin 2013;65:248-254.
Fischer J, Colls P, Escudero T, Munné S. Preimplantation genetic diagnosis (PGD) improves pregnancy outcome for translocation carriers with a history of recurrent losses. Fertil Steril 2010;94:283-289.
Rodríguez L, Martínez-Fernández ML, Mansilla E, Mendioroz J, et al. Screening for subtelomeric chromosome alteration in a consecutive series of newborns with congenital defects. Clin Dysmorphol 2008;17:5-12.
Martínez-Frías ML, Martínez-Fernández ML. A highly specific coding system for structural chromosomal alterations. Am J Med Genet A 2013;161A:732-736.
Brown T, Robertson FW, Dawson BM, Hanlin SJ, et al. Individual variation of centric heterochromatin in man. Hum Genet 1980;55:367-373.
Bashin M. Human population cytogenetics: a review. Int J Hum Genet 2005;5:83-152.
Gadner RJ, Stuherland GR. Variant chromosomes and abnormalities of no phenotypic consequence. In: Gadner RJ, Stuherland GR, Shaffer, editors. Chromosome abnormalities and genetic counselling. USA: Oxford University Press, 2012;257-268.
Minocherhomji S, Athalye AS, Madon PF, Kulkarni D, et al. A case-control study identifying chromosomal polymorphic variations as forms of epigenetic alterations associated with the infertility phenotype. Fertil Steril 2009;92:88-95.
Cortés-Gutiérrez EI, Cerda-Flores RM, Dávila-Rodríguez MI, et al. Chromosomal abnormalities and polymorphisms in Mexican infertile men. Arch Andrology 2004;50:261- 265.
Madon PF, Athalye AS, Parikh FR. Polymorphic variants on chromosomes probable play a significant role in infertility. Reprod Biomed Online 2005;11:726-732.
Poveda M, Rubio T, Ochando I, Gil L, et al. Las variantes cromosómicas afectan la calidad embrionaria. Rev Asoc Est Biol Rep 2010;15:19-23.
Dubey S, Chowdhury M, Prahalad B, et al. Cytogenetic causes for recurrent spontaneous abortion–an experience of 742 couples (1484 cases). Indian J Hum Gen 2005;11:94-98.
Iyer P, Wani L, Joshi S, et al. Cytogenetic investigations in couples with repeated miscarriages and malformed children: report of a novel insertion. Reproductive BioMedicine Online 2007;14:314-321.
De la Fuente-Cortés BE, Cerda-Flores RM, Dávila-Rodríguez MI, García-Vielma C, et al. Chromosomal abnormalities and polymorphic variants in couples with repeated miscarriage in Mexico. Reprod Biomed Online 2009;18:543-548.
Probst AV, Almouzni G. Pericentric heterochromatin: dynamic organization during early development in mammals. Differentiation 2008;76:15-23.
Assou S, Boumela I, Haouzi D, Anahory T, et al. Dynamic changes in gene expression during human early embryo development: from fundamental aspects to clinical applications. Hum Reprod Update 2011;17:272-290.
Ardoy M, Calderón G. Criterios ASEBIR de valoración morfológica de oocitos, embriones tempranos y blastocistos humanos. 2ª ed. Madrid: Asociación para el Estudio de la Biología de la Reproducción, 2008.
Kayhan Y, Basak B, Bulent U. Is there a posible correlation between chromosomal variants and spermatogenesis? Int J Urol 2005;12:984-989.
Rueda J, Moreno JM, Ochando I, Gil L, et al. Chromosome heteromorphisms in infertile copules. Chromosome Res 2007;15:35-36.
García-Guixé E, Jiménez-Macedo A, Arjona, Giménez C, et al. Polimorfismos heterocromáticos y riesgo incrementado de aneuploidías en embriones preimplantacionales. Rev Iberoam Fert Rep Hum 2010;27:214.
Craig JM, Wong NC. Epigenetics: A referente manual. Great Britain: Caister Academic Press, 2011.
Dávila-Rodríguez MI, Cortés Gutiérrez EI, Cerda Flores RM, Pita M, et al. Constitutive heterochromatin polymorphisms in human chromosomes identified by whole comparative genomic hybridization. Eur J Histochem 2011;55:28.
Coco R, Arribere R. Nacer Bien. Consideraciones científicas, éticas y legales del inicio de la vida. Buenos Aires: Tiempo editorial, 2005;27.
Elder K and Cohen J. Human preimplantation embryo selection. Informa Healthcare.
Delhanty JD, Griffin DK, Handyside AH, Harper J, et al. Detection of aneuploidy and chromosomal mosaicism in human embryos during preimplantation sex determination by fluorescent in situ hybridisation (FISH). Hum Mol Genet 1993;2:1183-1185.
Angell RR, Aitken RJ, van Look PF, Lumsden MA, et al. Chromosome abnormalities in human embryos after in vitro fertilization. Nature 1983;303:336-338.
Kuliev A, Verlinsky Y. Preimplantation diagnosis: a realistic option for assisted reproduction and genetic practice. Curr Opin Obstet Gynecol 2005;2:179-183.
Handyside AH, Kontogianni EH, Hardy K, Winston RM. Pregnancies from biopsied human preimplantation embryos sexed by Y-specific DNA amplification. Nature 1990;344:768-770.
Anderson NL, Anderson NG. Proteome and proteomics: new technologies, new concepts, and new words. Electrophoresis 1998;19:1853-1861.
Wilkins MR, Pasquali C, Appel RD, Ou K, et al. From proteins to proteomes: Large scale protein identification by two-dimensional electrophoresis and arnino acid analysis. Nature Biotechnology 1996;1:61-65.
Hanash SM, Pitteri SJ, Faca VM. Mining the plasma proteome for cancer biomarkers. Nature 2008;452:571-579.
Katz-Jaffe MG, Gardner DK. Symposium: Innovative techniques in human embryo viability assessment. Can proteomics help to shape the future of human assisted conception? RBM Online 2008;4:497-501.
Weiss W, Görg A. High-resolution two-dimensional electrophoresis. Methods Mol Biol 2009;564:13-32.
Latham KE, Garrels JI, Chang C, Solter D. Analysis of embryonic mouse development: construction of a highresolution, two-dimensional gel protein database. Appl Theor Electrophor 1992;6:163-170.
Shi CZ, Collins HW, Garside WT, Buettger CW, et al. Protein databases for compacted eight-cell and blastocyst-stage mouse embryos. Mol Reprod Dev 1994;1:34-47.
Navarrete Santos A, Tonack S, Kirstein M, Kietz S, et al. Two insulin-responsive glucose transporter isoforms and the insulin receptor are developmentally expressed in rabbit preimplantation embryos. Reproduction 2004;128:503-516.
Sutovsky P, Manandhar G, Laurincik J, Letko J. Expression and proteomic analysis of mammalian preimplantation embryonic development. Reproduction 2005;129:269- 282.
Katz-Jaffe MG, Linck DW, Schoolcraft WB, Gardner DK. A proteomic analysis of mammalian preimplantation embryonic development. Reproduction 2005;130:899-905.
Katz-Jaffe MG, Gardner DK, Schoolcraft WB. Proteomic analysis of individual human embryos to identify novel biomarkers of development and viability. Fert Steril 2006;85:101-107.
González RR, Caballero-Campo P, Jasper M, Mercader A, et al. Leptin and leptin receptor are expressed in the human endometrium and endometrial leptin secretion is regulated by human blastocyst. J Clin Endocrinol Metab 2000;85:4883-4888.
Díaz-Cueto L, Stein P, Jacobs A, Schultz RM, et al. Modulation of mouse preimplantation embryo development by acrogranin (epithelin/granulin precursor). Dev Biol 2000; 217:406-418.
Katz-Jaffe MG, Schoolcraft WB, Gardner DK. Analysis of protein expression (secretome) by human and mouse preimplantation embryos. Fertil Steril 2006;86:678-685.
Telford NA, Watson AJ, Schultz GA. Transition from maternal to embryonic control in early mammalian develop ment a comparision of several species. Mol Reprod Dev 1990;26:90-100.
Wang HM, Zhang X, Qian D, Lin HY, et al. Effect of ubiquitinproteasome pathway on mouse blastocyst implantation and expression of matrix metalloproteinases-2 and -9. Biol Reprod 2004;70:481-487.
Katz-Jaffe MG, Stevens J, Kearns WG, Gardner DK, et al. Relationship between embryonic secretome and chromosomal abnormalities in human IVF. Fertil Steril 2006;86:57.
Domínguez F, Gadea B, Esteban FJ, Horcajadas JA, et al. Comparative protein-profile analysis of implanted versus non-implanted human blastocyst. Hum Reprod 2008;23:1993-2000.
Robertson SA. GM-CFS regulation of embryo development and pregnancy. Cytokine Grownh Factor Rev 2007;18:287- 298.
Seli E, Sakkas D, Scott R, Kwok SC, et al. Noninvasive metabolomics profiling of embryo culture media using Raman and near-infrared spectroscopy correlates with reproductive potential of embryo in women undergoing in vitro fertilization. Fertil Steril 2007;88:1350-1357.