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Evolução dos índices de proliferação celular e apoptose em placentas de ratas com diabete grave : relação com glicemia materna e o resultado perinatal /Costa, Elaine Cristina Nunes Fagundes. January 2002 (has links)
Resumo: Não existem relatos sobre estudo concomitante de proliferação celular e apoptose placentária em ratas com diabete grave que é modelo de RCIU. O objetivo foi definir a técnica para estudar os índices de proliferação celular e de apoptose na placenta de ratas com diabete grave, no 18° e 21° dias de prenhez. Ratas Wistar prenhes constituíram quatro grupos experimentais, de acordo com a presença ou não de diabete, induzido pelo Streptozotocin e da idade de resolução da prenhez no 18º e 21º dias. Foram colhidas as placentas e analisadas a proliferação celular pelo método do PCNA e a apoptose pelos métodos de HE e TUNEL. Os dados foram comparados pelos testes t ou de Mann- Whitney. O índice de proliferação celular foi menor no grupo diabético de 21 dias em relação aos outros grupos, sendo que tanto o HE como o TUNEL detectaram esses índices menores no grupo diabético de 21 dias. A análise da apoptose pelo TUNEL, com índices apresentados por área de tecido placentário, parece ser mais adequada que o HE, pela rapidez na leitura das lâminas e pelos maiores índices observados. Os índices de PCNA e apoptose placentários por campo e por mm2, foram menores nos grupos diabéticos no 21° dia da prenhez. No 18° dia, estas análises foram equivalentes nos grupos controle e diabético; não houve correlação entre os índices de PCNA e apoptose no 18° e no 21° dias, nos grupos controle e diabético. / Abstract: There are no reports of placental studies of cellular proliferation and apoptosis in rats with severe diabetes, that is a IUGR (inter-uterine growth restriction) model. The aim of this study was to define a technique for studying cell proliferation and placental apoptosis of rats with severe diabetes, on the 18th and 21st days of pregnancy. Pregnant Wistar rats were divided into four experimental groups, with and without diabetes, induced by Streptozotocin, and pregnancy time of 18 and 21 days resolution. Placentae were collected and cell proliferation was analyzed by the PCNA method, and apoptosis by HE and TUNEL methods; and the data were compared by t tests or Mann-Whitney. The cell proliferation rate was lower in the diabetic group of 21 days pregnancy, in both HE and TUNEL tests. Analyses of apoptosis by TUNEL technique wich was presented by placental tissue area, seemed to be more adequate than HE, due to quickness on slide reading, and by the higher observed indexes. The indexes of PCNA and placental apoptosis by sight and in mm2 were lower in the diabetic groups on the pregnancy 21st day. On the 18th day, these analyses showed similar values in the control and the diabetic groups; there was no correlation between PCNA and apoptosis indexes on the 18th and on the 21st days, in control and diabetic groups. / Orientador: Marilza Vieira Cunha Rudge / Coorientador: Luís Fernando Barbisan / Doutor
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Evolução dos índices de proliferação celular e apoptose em placentas de ratas com diabete grave: relação com glicemia materna e o resultado perinatalCosta, Elaine Cristina Nunes Fagundes [UNESP] January 2002 (has links) (PDF)
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costa_ecnf_dr_botfm.pdf: 894781 bytes, checksum: 2aef88e3eb9258a9238181931845d932 (MD5) / Não existem relatos sobre estudo concomitante de proliferação celular e apoptose placentária em ratas com diabete grave que é modelo de RCIU. O objetivo foi definir a técnica para estudar os índices de proliferação celular e de apoptose na placenta de ratas com diabete grave, no 18° e 21° dias de prenhez. Ratas Wistar prenhes constituíram quatro grupos experimentais, de acordo com a presença ou não de diabete, induzido pelo Streptozotocin e da idade de resolução da prenhez no 18º e 21º dias. Foram colhidas as placentas e analisadas a proliferação celular pelo método do PCNA e a apoptose pelos métodos de HE e TUNEL. Os dados foram comparados pelos testes t ou de Mann- Whitney. O índice de proliferação celular foi menor no grupo diabético de 21 dias em relação aos outros grupos, sendo que tanto o HE como o TUNEL detectaram esses índices menores no grupo diabético de 21 dias. A análise da apoptose pelo TUNEL, com índices apresentados por área de tecido placentário, parece ser mais adequada que o HE, pela rapidez na leitura das lâminas e pelos maiores índices observados. Os índices de PCNA e apoptose placentários por campo e por mm2, foram menores nos grupos diabéticos no 21° dia da prenhez. No 18° dia, estas análises foram equivalentes nos grupos controle e diabético; não houve correlação entre os índices de PCNA e apoptose no 18° e no 21° dias, nos grupos controle e diabético. / There are no reports of placental studies of cellular proliferation and apoptosis in rats with severe diabetes, that is a IUGR (inter-uterine growth restriction) model. The aim of this study was to define a technique for studying cell proliferation and placental apoptosis of rats with severe diabetes, on the 18th and 21st days of pregnancy. Pregnant Wistar rats were divided into four experimental groups, with and without diabetes, induced by Streptozotocin, and pregnancy time of 18 and 21 days resolution. Placentae were collected and cell proliferation was analyzed by the PCNA method, and apoptosis by HE and TUNEL methods; and the data were compared by t tests or Mann-Whitney. The cell proliferation rate was lower in the diabetic group of 21 days pregnancy, in both HE and TUNEL tests. Analyses of apoptosis by TUNEL technique wich was presented by placental tissue area, seemed to be more adequate than HE, due to quickness on slide reading, and by the higher observed indexes. The indexes of PCNA and placental apoptosis by sight and in mm2 were lower in the diabetic groups on the pregnancy 21st day. On the 18th day, these analyses showed similar values in the control and the diabetic groups; there was no correlation between PCNA and apoptosis indexes on the 18th and on the 21st days, in control and diabetic groups.
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Functional Differentiation Of The Human Placenta : Insights From The Expression Of Two Developmentally - Regulated GenesRao, M Rekha 11 1900 (has links)
Placenta is a transient association of the fetal and maternal tissues, that develops during pregnancy, in most viviparous animals. The evolution of placenta ensured the development of the fetus inside the womb of the mother, providing a protected environment for the development of the fetus, and preventing the loss of progeny due to unfavorable environmental conditions. Because it is strategically poised at the maternal and fetal interface, the placenta is ideally suited to carry out alimentary, respiratory and excretory functions for the developing fetus. In addition, it serves as an immunological barrier preventing the rejection of the fetal semi-allograft, by the maternal immune system. Furthermore, the placenta elaborates a variety of protein, polypeptide and steroid hormones. These include growth factors, growth factor receptors, neuropeptides, opioids, progesterone and estrogen, whose secretion is dependent on the gestational age of the placenta and its differentiation status.
The human placenta, adapts itself remarkably to cater to the changing requirements of the developing fetus. For instance, during the first trimester of pregnancy, the placenta is an actively dividing, a highly invasive and a rapidly differentiating organ; while near term, it represents a fully differentiated and a non-invasive unit. Furthermore, the placenta of the first trimester and that at term differ in their hormone profiles, extents of apoptosis, expression of several transcription factors, etc. This dramatic change in the phenotype of the human placenta can be considered to be the outcome of an intrinsically programmed pattern of differentiation, which may be referred to as the functional differentiation of the placenta. It may be hypothesized therefore, that this functional differentiation could be brought about by the differential expression of genes in the first trimester and the term placenta.
The objectives of the present study were:
1. To gain an insight into this process of " functional differentiation” by investigating the differential expression of genes in the two developmentally distinct stages during gestation, viz. during the first trimester and at term.
2. To understand the functional relevance of the differentially expressed genes.
A general introduction of the human placenta, describing the importance of differential expression in modulating placental function, is discussed in chapter 1. The functions of the human placenta along with a
brief description of its development and differentiation are also briefly described.
A Differential Display RT-PCR-based (DD RT-PCR) approach, using total RNA from the first-trimester and term placental villi, was employed to display the differentially expressed genes in the first trimester and the term placenta. The display so generated was used to identify a few differentially expressed cDNAs. This study was aimed at understanding the functional significance of the transcripts which were identified from the display, rather than just concentrate on documenting the differences in the gene expression patterns in the first trimester and the term placental tissue. A detailed description of the methodology adopted for performing DD-PCR using placental tissue, discussing the advantages and disadvantages of using differential display PCR, is described in chapter2.
The use of DD-PCR for studying differential gene expression in the human placenta was validated by the finding that one of the cDNAs that was differentially expressed in the first trimester placental tissue, is a fragment of β-hCG cDNA. It is well documented that the differential expression of the β-subunit of hCG (human chorionic gondatrophin) during the first eight weeks of gestation is the rate limiting step in the synthesis and secretion of the functional hormone, which comprises the α and the β-subunits. Furthermore, the use of the model system viz., the first trimester and term placental tissue, was also validated for carrying out DD-PCR by ensuring that all placental samples used for DD analysis were free of endometrial contamination. A detailed description of optimization and validation of DD-PCR in human placental tissues is given in chapter 2.
Cloning and sequencing of yet another cDNA from the first trimester differential display revealed that it is T-Plastin. T-Plastin is a member of a family of proteins that are involved in actin-bundling. Northern blot analysis and immunohistochemical studies using an antibody generated to a peptide corresponding to human T-Plastin, confirmed its differential expression and localization in the first trimester placenta. Considering the fact that several carcinomas show enhanced expression of T-Plastin, we tested the hypothesis that its differential expression is correlated with the proliferative potential of the first-trimester placenta It was observed that the first-trimester tissue expressed high levels of beta-actin as compared to the term placental tissue. This is in agreement with the up-regulation of beta-actin following mitogenic stimulation/proliferation and during neoplastic transformation or transformation-associated invasive behaviour of cells, two characteristic features shared by the early placenta with cancerous tissues. Based on our studies and available information in the literature, it is proposed that T-Plastin expression in the first trimester placenta is a growth-associated phenomenon which is partially responsible for the tumor-like phenotype of the first trimester tissue. Studies carried out with the partial T-Plastin cDNA clone that was isolated from the first trimester differential display, are presented in chapter 3.
Sequencing of yet another cDNA clone identified from the term placental differential display, T-18 revealed that it had no homology to any known sequence in the nucleotide or est databases. The sequence corresponding to this clone was submitted to the GenBank and was assigned an accession number- AF089811. The differential expression of T-18 was confirmed by Northern blot analysis and RT-PCR analysis. Attempts were made to isolate the full-length cDNA corresponding to T-18 from a commercially available library from Clontech. However, repeated trials to identify the clone corresponding to T-18 did not yield any positive results. However, a genome database search revealed that T-18 was a portion of a large contig contained in chromosome 15. Analysis of the annotated gene sequences in and around the region in which T-18 is located in chromosome 15, revealed that there are very few ests reported in this contig and quite a few repeat sequences reported. Interestingly, it was observed that 6 kb downstream of the region in which T-18 is located, there was an est that had homology to a Bcl-2 precursor protein (an evolutionarily conserved, anti-apoptotic protein, capable of conferring protection against death-inducing signals) and the death adaptor protein, CRADD {Caspase and RIP adapter with death domain). Further updating of the ests in the database might probably be of help in the identification of the full-length cDNA corresponding to T-18 and confirm as to whether T-18 is a part of the gene/gene cluster that comprises the afore-mentioned est. An account of the identification and cloning of T-18 from the term placenta and the attempts to isolate the full-length cDNA clone corresponding to T-18 from a term placental cDNA library, is described in chapter 4.
In the absence of any information on the identity of T-18, a study to understand the functional significance of T-18 expression was carried out. Since it was not possible to carry out studies pertaining to the temporal expression of T-18 throughout gestation on the human placenta for ethical reasons, alternate animal/organ models were employed to study T-18 expression. Rat placenta and rat Corpus Luteum (CL) were chosen as alternate models for studying T-18 expression as these two organs/tissues underwent dynamic changes in their function throughout pregnancy. For instance, it is well known that CL is the primary source of progesterone for maintaining pregnancy in the rat and that the progesterone secreting capacity of the luteal cells peak on day 16 of gestation and decline thereafter. Interestingly, a common feature among all the tissues that were chosen for investigating the regulation of T-18 expression, is the fact that they underwent apoptosis with increase in gestational age. The expression of T-18, in tissues exhibiting increased incidence of apoptosis suggested that T-18 maybe an apoptosis-associated gene.
Using an explant culture model it was demonstrated that placental villi when cultured in vitro underwent spontaneous apoptosis and that the levels of T-18 message increased, under these conditions. Furthermore, this spontaneous induction of apoptosis in explant cultures could be blocked when villi were cultured in the presence of superoxide dismutase, a free radical scavenging enzyme. In addition, the expression of T-18 was shown to be modulated following treatment with SOD, or in response to oxidative stress. These studies clearly indicate a role for T-18 in placental apoptosis and moreover, implicate the usefulness of explant culture to examine the molecular mechanisms involved in placental apoptosis. Furthermore, the expression of the anti- and pro-apoptotic genes, bcl-x and bax respectively, were investigated, in an attempt to elucidate the signalling pathway(s) that led to the activation of an important downstream protease, caspase-3, in placental apoptosis. The present study revealed that induction of apoptosis in the placenta in vitro involved a bcl/bax independent, caspase-3 dependant pathway. The validation of an explant culture model for studying placental apoptosis and data pertaining to the role of T-18, bcl-x, bax and CPP32 in placental apoptosis, in response to oxidative stress, are presented in chapter 5.
The last section titled general discussion summarizes the work carried out in this study and proposes a model for the apoptotic mechanism(s) that may be operating in placenta
In conclusion, the present study has led to the identification of two developmentally-regulated factors, T-Plastin and T-18 in the first trimester and term placenta, respectively. The differential expression of these genes, in addition to several other molecular players, is proposed to be responsible for the overall functional differentiation of the placenta through the course of gestation.
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