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Dive into the research topics where María de Lourdes Segura-Valdez is active.

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Featured researches published by María de Lourdes Segura-Valdez.


Microscopy and Microanalysis | 2005

Electron Microscopy Analysis of the Nucleolus of Trypanosoma cruzi

Gabriel López-Velázquez; Roberto Hernández; Imelda López-Villaseñor; Horacio Reyes-Vivas; María de Lourdes Segura-Valdez; Luis Felipe Jiménez-García

The nucleolus is the main site for synthesis and processing of ribosomal RNA in eukaryotes. In mammals, plants, and yeast the nucleolus has been extensively characterized by electron microscopy, but in the majority of the unicellular eukaryotes no such studies have been performed. Here we used ultrastructural cytochemical and immunocytochemical techniques as well as three-dimensional reconstruction to analyze the nucleolus of Trypanosoma cruzi, which is an early divergent eukaryote of medical importance. In T. cruzi epimastigotes the nucleolus is a spherical intranuclear ribonucleoprotein organelle localized in a relatively central position within the nucleus. Dense fibrillar and granular components but not fibrillar centers were observed. In addition, nuclear bodies resembling Cajal bodies were observed associated to the nucleolus in the surrounding nucleoplasm. Our results provide additional morphological data to better understand the synthesis and processing of the ribosomal RNA in kinetoplastids.


PLOS ONE | 2015

Drug Development in Conformational Diseases: A Novel Family of Chemical Chaperones that Bind and Stabilise Several Polymorphic Amyloid Structures

Marquiza Sablón-Carrazana; Isaac Fernández; Alberto Bencomo; Reyna Lara-Martínez; Suchitil Rivera-Marrero; Guadalupe Domínguez; Rafaela Pérez-Perera; Luis Felipe Jiménez-García; Nelly Altamirano-Bustamante; Massiel Diaz-Delgado; Fernand Vedrenne; Lina Rivillas-Acevedo; Karina Pasten-Hidalgo; María de Lourdes Segura-Valdez; Sergio Islas-Andrade; Eulalia Garrido-Magaña; Alejandro Perera-Pintado; Anaís Prats-Capote; Chryslaine Rodríguez-Tanty; Myriam M Altamirano-Bustamante

The increasing prevalence of conformational diseases, including Alzheimers disease, type 2 Diabetes Mellitus and Cancer, poses a global challenge at many different levels. It has devastating effects on the sufferers as well as a tremendous economic impact on families and the health system. In this work, we apply a cross-functional approach that combines ideas, concepts and technologies from several disciplines in order to study, in silico and in vitro, the role of a novel chemical chaperones family (NCHCHF) in processes of protein aggregation in conformational diseases. Given that Serum Albumin (SA) is the most abundant protein in the blood of mammals, and Bovine Serum Albumin (BSA) is an off-the-shelf protein available in most labs around the world, we compared the ligandability of BSA:NCHCHF with the interaction sites in the Human Islet Amyloid Polypeptide (hIAPP):NCHCHF, and in the amyloid pharmacophore fragments (Aβ17–42 and Aβ16–21):NCHCHF. We posit that the merging of this interaction sites is a meta-structure of pharmacophore which allows the development of chaperones that can prevent protein aggregation at various states from: stabilizing the native state to destabilizing oligomeric state and protofilament. Furthermore to stabilize fibrillar structures, thus decreasing the amount of toxic oligomers in solution, as is the case with the NCHCHF. The paper demonstrates how a set of NCHCHF can be used for studying and potentially treating the various physiopathological stages of a conformational disease. For instance, when dealing with an acute phase of cytotoxicity, what is needed is the recruitment of cytotoxic oligomers, thus chaperone F, which accelerates fiber formation, would be very useful; whereas in a chronic stage it is better to have chaperones A, B, C, and D, which stabilize the native and fibril structures halting self-catalysis and the creation of cytotoxic oligomers as a consequence of fiber formation. Furthermore, all the chaperones are able to protect and recondition the cerebellar granule cells (CGC) from the cytotoxicity produced by the hIAPP20–29 fragment or by a low potassium medium, regardless of their capacity for accelerating or inhibiting in vitro formation of fibers. In vivo animal experiments are required to study the impact of chemical chaperones in cognitive and metabolic syndromes.


Biology of the Cell | 2002

Lacandonia granules are present in Ginkgo biloba cell nuclei

Jaime Jiménez-Ramírez; Lourdes Teresa Agredano-Moreno; María de Lourdes Segura-Valdez; Luis Felipe Jiménez-García

Summry— Lacandonia schismatica is a rare flowering plant with the sex organs spatially inverted. Several aspects of its cell biology are now known. Interestingly, within the cell nucleus, the chromatin is reticulated and it is associated to a novel structure named Lacandonia granules, a very abundant ribonucleoprotein particle showing similarities to perichromatin and Balbiani ring granules, which are involved in nuclear mRNA metabolism. To see whether these particles are present in other plants, we study the nucleus of Ginkgo biloba, a non‐flowering plant. Light, electron and atomic force microscopy show that the cell nuclei of G. biloba are reticulated. Ultrastructural analysis showed that in the nucleoplasm, abundant intranuclear particles 32 nm in diameter are present. The EDTA regressive staining suggested that they contain RNA. Ultrastructural in situ hybridization confirmed the presence of RNA in these particles. Therefore, we conclude that the nuclei of G. biloba are reticulated and contain Lacandonia granules. We suggest that these particles may also be present in other plants.


Biology of the Cell | 2002

Cellular organization of pre-mRNA splicing factors in several tissues. Changes in the uterus by hormone action

R. George-Téllez; María de Lourdes Segura-Valdez; L. González-Santos; Luis Felipe Jiménez-García

In the mammalian cell nucleus, splicing factors are distributed in nuclear domains known as speckles or splicing factor compartments (SFCs). In cultured cells, these domains are dynamic and reflect transcriptional and splicing activities. We used immunofluorescence and confocal microscopy to monitor whether splicing factors in differentiated cells display similar features. Speckled patterns are observed in rat hepatocytes, β‐cells, bronchial and intestine epithelia and also in three cell types of the uterus. Moreover, the number, distribution and sizes of the speckles vary among them. In addition, we studied variations in the circular form (shape) of speckles in uterine cells that are transcriptionally modified by a hormone action. During proestrus of the estral cycle, speckles are irregular in shape while in diestrus I they are circular. Experimentally, in castrated rats luminal epithelial cells show a pattern where speckles are dramatically rounded, but they recover their irregular shape rapidly after an injection of estradiol. The same results were observed in muscle and gland epithelial cells of the uterus. We concluded that different speckled patterns are present in various cells types in differentiated tissues and that these patterns change in the uterus depending upon the presence or absence of hormones such as estradiol.


Histochemistry and Cell Biology | 2018

Visualization of internal in situ cell structure by atomic force microscopy

María de Lourdes Segura-Valdez; Lourdes Teresa Agredano-Moreno; Alma Zamora-Cura; Reyna Lara-Martínez; Luis Felipe Jiménez-García

Light and electron microscopy have been used to study cell structure for many years, but atomic force microscopy is a more recent technique used to analyze cells, mainly due to the absence of techniques to prepare the samples. Isolated molecules or organelles, whole cells, and to a lesser extent in situ cell structure have been observed by different atomic force microscopy imaging modes. Here, we review efforts intended to analyze in situ the cell structures using approaches involving imaging of the surface of semithin sections of samples embedded in resin and sections prepared with an ultramicrotome. The results of such studies are discussed in relation to their implications to analyze the fine structure of organelles at the nanoscale in situ at enhanced resolution compared to light microscopy.


Microscopy and Microanalysis | 2016

Nucleologenesis in Trypanosoma cruzi.

Tomás Nepomuceno-Mejía; Reyna Lara-Martínez; Roberto Hernández; María de Lourdes Segura-Valdez; Luis Felipe Jiménez-García

Nucleolar assembly is a cellular event that requires the synthesis and processing of ribosomal RNA, in addition to the participation of pre-nucleolar bodies (PNBs) at the end of mitosis. In mammals and plants, nucleolar biogenesis has been described in detail, but in unicellular eukaryotes it is a poorly understood process. In this study, we used light and electron microscopy cytochemical techniques to investigate the distribution of nucleolar components in the pathway of nucleolus rebuilding during closed cell division in epimastigotes of Trypanosoma cruzi, the etiologic agent of American trypanosomiasis. Silver impregnation specific for nucleolar organizer regions and an ethylenediaminetetraacetic acid regressive procedure to preferentially stain ribonucleoprotein revealed the conservation and dispersion of nucleolar material throughout the nucleoplasm during cell division. Furthermore, at the end of mitosis, the argyrophilic proteins were concentrated in the nucleolar organizer region. Unexpectedly, accumulation of nucleolar material in the form of PNBs was not visualized. We suggest that formation of the nucleolus in epimastigotes of T. cruzi occurs by a process that does not require the concentration of nucleolar material within intermediate nuclear bodies such as mammalian and plant PNBs.


Anatomical Record-advances in Integrative Anatomy and Evolutionary Biology | 2016

Morphological Studies of Nucleologenesis in Giardia lamblia

Reyna Lara-Martínez; María de Lourdes Segura-Valdez; Ignacio De la Mora-De la Mora; Gabriel López-Velázquez; Luis Felipe Jiménez-García

The nucleolus is a nuclear organelle involved in ribosome biogenesis. In most eukaryotes this structure disperses during prophase through anaphase and reorganizes at telophase by a process known as nucleologenesis. This process involves new transcription of ribosomal DNA at the nucleolar organizer region and the formation of prenucleolar bodies fusing to it. In Giardia lamblia, for a long time considered the only anucleolated eukaryote, a very small nucleolus has been recently described. In order to evaluate whether nucleologenesis is also present in Giardia, we analyzed the distribution of nucleolar material during telophase using different light and electron microscopy techniques including silver staining for the nucleolar organizer. Results indicate that in G. lamblia, nucleolar elements persist mainly as an intranuclear peripheral organelle during all stages of division, including telophase, however, no prenucleolar bodies are detected in the nucleoplasm. Therefore, in the parasite, nucleolar material is present throughout cell division including telophase and formation of prenucleolar bodies may not be required for nucleologenesis. Anat Rec, 299:549–556, 2016.


Molecular Biology of the Cell | 1994

Nucleologenesis: U3 snRNA-containing prenucleolar bodies move to sites of active pre-rRNA transcription after mitosis.

Luis Felipe Jiménez-García; María de Lourdes Segura-Valdez; Robert L. Ochs; Lawrence I. Rothblum; Ross D. Hannan; David L. Spector


International Journal for Parasitology | 2008

Identification of nucleoli in the early branching protist Giardia duodenalis.

Luis Felipe Jiménez-García; Guadalupe Zavala; Bibiana Chávez-Munguía; María del Pilar Ramos-Godínez; Gabriel López-Velázquez; María de Lourdes Segura-Valdez; Cecilia Montañez; Adrian B. Hehl; Raúl Argüello-García; Guadalupe Ortega-Pierres


Molecular Reproduction and Development | 2003

c-fos and estrogen receptor gene expression pattern in the rat uterine epithelium during the estrous cycle

C. Adriana Mendoza-Rodríguez; Horacio Merchant-Larios; María de Lourdes Segura-Valdez; Norma Moreno-Mendoza; María Esther Cruz; Paola Arteaga-López; Ignacio Camacho-Arroyo; Roberto Domínguez; Marco Cerbón

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Luis Felipe Jiménez-García

National Autonomous University of Mexico

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Reyna Lara-Martínez

National Autonomous University of Mexico

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Lourdes Teresa Agredano-Moreno

National Autonomous University of Mexico

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Clara H. Ramos

National Autonomous University of Mexico

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Esteban Martínez

National Autonomous University of Mexico

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Gabriel López-Velázquez

National Autonomous University of Mexico

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Gerardo H. Vázquez-Nin

National Autonomous University of Mexico

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Guadalupe Zavala

National Autonomous University of Mexico

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Cristina Negrete García

National Autonomous University of Mexico

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Horacio Merchant-Larios

National Autonomous University of Mexico

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