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  1. Article ; Online: 3′-UTR of the SARS-CoV-2 genome as a possible source of piRNAs

    María Teresa Hernández-Huerta / Laura Pérez-Campos Mayoral / Carlos Alberto Matias-Cervantes / Carlos Romero Díaz / Eli Cruz Parada / Eduardo Pérez-Campos Mayoral / Rafael Baltiérrez-Hoyos / Margarito Martínez Cruz / Gabriel Mayoral Andrade / Eduardo Pérez-Campos

    Genes and Diseases, Vol 10, Iss 3, Pp 668-

    2023  Volume 670

    Keywords Medicine (General) ; R5-920 ; Genetics ; QH426-470
    Language English
    Publishing date 2023-05-01T00:00:00Z
    Publisher Elsevier
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  2. Article ; Online: Interaction of piRNA-like sequences from the 3′-UTR of SARS-CoV-2 with mRNA regions

    Laura Pérez-Campos Mayoral / María Teresa Hernández-Huerta / Carlos Romero Díaz / Carlos Alberto Matias-Cervantes / Eduardo Pérez-Campos Mayoral / Margarito Martínez Cruz / Juan de Dios Ruiz-Rosado / Edgar Gustavo Ramos Martínez / Marco Antonio Sánchez Medina / Eduardo Pérez-Campos

    Genes and Diseases, Vol 10, Iss 6, Pp 2282-

    2023  Volume 2284

    Keywords Medicine (General) ; R5-920 ; Genetics ; QH426-470
    Language English
    Publishing date 2023-11-01T00:00:00Z
    Publisher KeAi Communications Co., Ltd.
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  3. Article ; Online: The Role of B Cell and T Cell Glycosylation in Systemic Lupus Erythematosus

    Ivan Ramos-Martínez / Edgar Ramos-Martínez / Marco Cerbón / Armando Pérez-Torres / Laura Pérez-Campos Mayoral / María Teresa Hernández-Huerta / Margarito Martínez-Cruz / Alma Dolores Pérez-Santiago / Marco Antonio Sánchez-Medina / Iván Antonio García-Montalvo / Edgar Zenteno / Carlos Alberto Matias-Cervantes / Víctor Ojeda-Meixueiro / Eduardo Pérez-Campos

    International Journal of Molecular Sciences, Vol 24, Iss 1, p

    2023  Volume 863

    Abstract: Glycosylation is a post-translational modification that affects the stability, structure, antigenicity and charge of proteins. In the immune system, glycosylation is involved in the regulation of ligand–receptor interactions, such as in B-cell and T-cell ...

    Abstract Glycosylation is a post-translational modification that affects the stability, structure, antigenicity and charge of proteins. In the immune system, glycosylation is involved in the regulation of ligand–receptor interactions, such as in B-cell and T-cell activating receptors. Alterations in glycosylation have been described in several autoimmune diseases, such as systemic lupus erythematosus (SLE), in which alterations have been found mainly in the glycosylation of B lymphocytes, T lymphocytes and immunoglobulins. In immunoglobulin G of lupus patients, a decrease in galactosylation, sialylation, and nucleotide fucose, as well as an increase in the N -acetylglucosamine bisector, are observed. These changes in glycoisolation affect the interactions of immunoglobulins with Fc receptors and are associated with pericarditis, proteinuria, nephritis, and the presence of antinuclear antibodies. In T cells, alterations have been described in the glycosylation of receptors involved in activation, such as the T cell receptor; these changes affect the affinity with their ligands and modulate the binding to endogenous lectins such as galectins. In T cells from lupus patients, a decrease in galectin 1 binding is observed, which could favor activation and reduce apoptosis. Furthermore, these alterations in glycosylation correlate with disease activity and clinical manifestations, and thus have potential use as biomarkers. In this review, we summarize findings on glycosylation alterations in SLE and how they relate to immune system defects and their clinical manifestations.
    Keywords autoimmune diseases ; glycans ; post-translational modifications ; lectins ; immunoglobulins ; T cells ; Biology (General) ; QH301-705.5 ; Chemistry ; QD1-999
    Subject code 610
    Language English
    Publishing date 2023-01-01T00:00:00Z
    Publisher MDPI AG
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  4. Article ; Online: Associations of Dynapenic Obesity and Sarcopenic Obesity with the Risk of Complications in COVID-19

    Laura Pérez-Campos Mayoral / Carlos Alberto Matias-Cervantes / Eduardo Pérez-Campos / Carlos Romero Díaz / Luis Ángel Laguna Barrios / María del Socorro Pina Canseco / Margarito Martínez Cruz / Eduardo Pérez-Campos Mayoral / Carlos Josué Solórzano Mata / Francisco Javier Rodal Canales / Héctor Martínez Ruíz / María Teresa Hernández-Huerta

    International Journal of Molecular Sciences, Vol 23, Iss 15, p

    2022  Volume 8277

    Abstract: Ageing is associated with changes in body composition, such as low muscle mass (sarcopenia), decreased grip strength or physical function (dynapenia), and accumulation of fat mass. When the accumulation of fat mass synergistically accompanies low muscle ... ...

    Abstract Ageing is associated with changes in body composition, such as low muscle mass (sarcopenia), decreased grip strength or physical function (dynapenia), and accumulation of fat mass. When the accumulation of fat mass synergistically accompanies low muscle mass or reduced grip strength, it results in sarcopenic obesity and dynapenic obesity, respectively. These types of obesity contribute to the increased risk of cardiovascular disease and mortality in the elderly, which could increase the damage caused by COVID-19. In this review, we associated factors that could generate a higher risk of COVID-19 complications in dynapenic obesity and sarcopenic obesity. For example, skeletal muscle regulates the expression of inflammatory cytokines and supports metabolic stress in pulmonary disease; hence, the presence of dynapenic obesity or sarcopenic obesity could be related to a poor prognosis in COVID-19 patients.
    Keywords sarcopenic obesity ; ageing ; COVID-19 ; complications ; dynapenic obesity ; Biology (General) ; QH301-705.5 ; Chemistry ; QD1-999
    Language English
    Publishing date 2022-07-01T00:00:00Z
    Publisher MDPI AG
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  5. Article ; Online: Interaction of Spike protein and lipid membrane of SARS-CoV-2 with Ursodeoxycholic acid, an in-silico analysis

    Francisco Javier Rodal Canales / Laura Pérez-Campos Mayoral / María Teresa Hernández-Huerta / Luis Manuel Sánchez Navarro / Carlos Alberto Matias-Cervantes / Margarito Martínez Cruz / Eli Cruz Parada / Edgar Zenteno / Edgar Gustavo Ramos-Martínez / Eduardo Pérez-Campos Mayoral / Carlos Romero Díaz / Eduardo Pérez-Campos

    Scientific Reports, Vol 11, Iss 1, Pp 1-

    2021  Volume 11

    Abstract: Abstract Numerous repositioned drugs have been sought to decrease the severity of SARS-CoV-2 infection. It is known that among its physicochemical properties, Ursodeoxycholic Acid (UDCA) has a reduction in surface tension and cholesterol solubilization, ... ...

    Abstract Abstract Numerous repositioned drugs have been sought to decrease the severity of SARS-CoV-2 infection. It is known that among its physicochemical properties, Ursodeoxycholic Acid (UDCA) has a reduction in surface tension and cholesterol solubilization, it has also been used to treat cholesterol gallstones and viral hepatitis. In this study, molecular docking was performed with the SARS-CoV-2 Spike protein and UDCA. In order to confirm this interaction, we used Molecular Dynamics (MD) in “SARS-CoV-2 Spike protein-UDCA”. Using another system, we also simulated MD with six UDCA residues around the Spike protein at random, naming this “SARS-CoV-2 Spike protein-6UDCA”. Finally, we evaluated the possible interaction between UDCA and different types of membranes, considering the possible membrane conformation of SARS-CoV-2, this was named “SARS-CoV-2 membrane-UDCA”. In the “SARS-CoV-2 Spike protein-UDCA”, we found that UDCA exhibits affinity towards the central region of the Spike protein structure of − 386.35 kcal/mol, in a region with 3 alpha helices, which comprises residues from K986 to C1032 of each monomer. MD confirmed that UDCA remains attached and occasionally forms hydrogen bonds with residues R995 and T998. In the presence of UDCA, we observed that the distances between residues atoms OG1 and CG2 of T998 in the monomers A, B, and C in the prefusion state do not change and remain at 5.93 ± 0.62 and 7.78 ± 0.51 Å, respectively, compared to the post-fusion state. Next, in “SARS-CoV-2 Spike protein-6UDCA”, the three UDCA showed affinity towards different regions of the Spike protein, but only one of them remained bound to the region between the region's heptad repeat 1 and heptad repeat 2 (HR1 and HR2) for 375 ps of the trajectory. The RMSD of monomer C was the smallest of the three monomers with a value of 2.89 ± 0.32, likewise, the smallest RMSF was also of the monomer C (2.25 ± 056). In addition, in the simulation of “SARS-CoV-2 membrane-UDCA”, UDCA had a higher affinity toward the virion-like membrane; ...
    Keywords Medicine ; R ; Science ; Q
    Subject code 612
    Language English
    Publishing date 2021-11-01T00:00:00Z
    Publisher Nature Portfolio
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  6. Article ; Online: miRNAs Contained in Extracellular Vesicles Cargo Contribute to the Progression of Idiopathic Pulmonary Fibrosis

    Jovito Cesar Santos-Álvarez / Juan Manuel Velázquez-Enríquez / Rosendo García-Carrillo / César Rodríguez-Beas / Alma Aurora Ramírez-Hernández / Edilburga Reyes-Jiménez / Karina González-García / Armando López-Martínez / Laura Pérez-Campos Mayoral / Sergio Roberto Aguilar-Ruiz / María de los Ángeles Romero-Tlalolini / Honorio Torres-Aguilar / Luis Castro-Sánchez / Jaime Arellanes-Robledo / Verónica Rocío Vásquez-Garzón / Rafael Baltiérrez-Hoyos

    Cells, Vol 11, Iss 1112, p

    An In Vitro Aproach

    2022  Volume 1112

    Abstract: Idiopathic pulmonary fibrosis (IPF) is a chronic, progressive lung disease. Lesions in the lung epithelium cause alterations in the microenvironment that promote fibroblast accumulation. Extracellular vesicles (EVs) transport proteins, lipids, and ... ...

    Abstract Idiopathic pulmonary fibrosis (IPF) is a chronic, progressive lung disease. Lesions in the lung epithelium cause alterations in the microenvironment that promote fibroblast accumulation. Extracellular vesicles (EVs) transport proteins, lipids, and nucleic acids, such as microRNAs (miRNAs). The aim of this study was to characterize the differentially expressed miRNAs in the cargo of EVs obtained from the LL97 and LL29 fibroblast cell lines isolated from IPF lungs versus those derived from the CCD19 fibroblast cell line isolated from a healthy donors. We characterized EVs by ultracentrifugation, Western blotting, and dynamic light scattering. We identified miRNAs by small RNA-seq, a total of 1144 miRNAs, of which 1027 were known miRNAs; interestingly, 117 miRNAs were novel. Differential expression analysis showed that 77 miRNAs were upregulated and 68 were downregulated. In addition, pathway enrichment analyses from the Gene Ontology and Kyoto Encyclopedia of Genomes identified several miRNA target genes in the categories, cell proliferation, regulation of apoptosis, pathways in cancer, and proteoglycans in cancer. Our data reveal that miRNAs contained in EVs cargo could be helpful as biomarkers for fibrogenesis, diagnosis, and therapeutic intervention of IPF.
    Keywords idiopathic pulmonary fibrosis ; extracellular vesicles ; fibroblasts ; small-RNA seq ; Biology (General) ; QH301-705.5
    Subject code 500
    Language English
    Publishing date 2022-03-01T00:00:00Z
    Publisher MDPI AG
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  7. Article ; Online: Obesity subtypes, related biomarkers & heterogeneity

    Laura Perez-Campos Mayoral / Gabriel Mayoral Andrade / Eduardo Perez-Campos Mayoral / Teresa Hernandez Huerta / Socorro Pina Canseco / Francisco J Rodal Canales / Héctor Alejandro Cabrera-Fuentes / Margarito Martinez Cruz / Alma Dolores Pérez Santiago / Juan José Alpuche / Edgar Zenteno / Hector Martínez Ruíz / Ruth Martínez Cruz / Julia Hernandez Jeronimo / Eduardo Perez-Campos

    Indian Journal of Medical Research, Vol 151, Iss 1, Pp 11-

    2020  Volume 21

    Abstract: Obesity is a serious medical condition worldwide, which needs new approaches and recognized international consensus in treating diseases leading to morbidity. The aim of this review was to examine heterogeneous links among the various phenotypes of ... ...

    Abstract Obesity is a serious medical condition worldwide, which needs new approaches and recognized international consensus in treating diseases leading to morbidity. The aim of this review was to examine heterogeneous links among the various phenotypes of obesity in adults. Proteins and associated genes in each group were analysed to differentiate between biomarkers. A variety of terms for classification and characterization within this pathology are currently in use; however, there is no clear consensus in terminology. The most significant groups reviewed include metabolically healthy obese, metabolically abnormal obese, metabolically abnormal, normal weight and sarcopenic obese. These phenotypes do not define particular genotypes or epigenetic gene regulation, or proteins related to inflammation. There are many other genes linked to obesity, though the value of screening all of those for diagnosis has low predictive results, as there are no significant biomarkers. It is important to establish a consensus in the terminology used and the characteristics attributed to obesity subtypes. The identification of specific molecular biomarkers is also required for better diagnosis in subtypes of obesity.
    Keywords adipose tissue - biomarkers - body fat - genome-wide association studies - heterogeneity - homa - obesity - subtypes ; Medicine ; R
    Language English
    Publishing date 2020-01-01T00:00:00Z
    Publisher Wolters Kluwer Medknow Publications
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  8. Article ; Online: Aggregation and Molecular Properties of β-Glucosidase Isoform II in Chayote ( Sechium edule )

    Alberto Cruz Rodríguez / Fabiola Anaid Sánchez Esperanza / Eduardo Pérez-Campos / María Teresa Hernández-Huerta / Laura Pérez-Campos Mayoral / Carlos Alberto Matias-Cervantes / Alexis Martínez Barras / Gabriel Mayoral-Andrade / Luis Ángel Santos Pineda / Aymara Judith Díaz Barrita / Edgar Zenteno / Carlos Romero Díaz / Ruth Martínez Cruz / Eduardo Pérez-Campos Mayoral / Edith Alhelí Bernabé Pérez / Alma Dolores Pérez Santiago / María del Socorro Pina-Canseco / Margarito Martínez Cruz

    Molecules, Vol 25, Iss 1699, p

    2020  Volume 1699

    Abstract: The presence of isoforms of β-glucosidase has been reported in some grasses such as sorghum, rice and maize. This work aims to extract and characterize isoform II in β-glucosidase from S. edule . A crude extract was prepared without buffer solution and ... ...

    Abstract The presence of isoforms of β-glucosidase has been reported in some grasses such as sorghum, rice and maize. This work aims to extract and characterize isoform II in β-glucosidase from S. edule . A crude extract was prepared without buffer solution and adjusted to pH 4.6. Contaminating proteins were precipitated at 4 °C for 24 h. The supernatant was purified by chromatography on carboxymethyl cellulose (CMC) column, molecular exclusion on Sephacryl S-200HR, and exchange anionic on QFF column. Electrophoretic analyzes revealed a purified enzyme with aggregating molecular complex on SDS-PAGE, Native-PAGE, and AU-PAGE. Twelve peptides fragments were identified by nano liquid chromatography-tandem mass spectrometry (nano LC-ESI-MS/MS), which presented as 61% identical to Cucurbita moschata β-glucosidase and 55.74% identical to β-glucosidase from Cucumis sativus , another Cucurbitaceous member. The relative masses which contained 39% hydrophobic amino acids ranged from 982.49 to 2,781.26. The enzyme showed a specificity to β- d -glucose with a K m of 4.59 mM, a V max value of 104.3 μM∙min −1 and a k cat of 10,087 μM∙min −1 using p -nitrophenyl-β-D-glucopyranoside. The presence of molecular aggregates can be attributed to non-polar amino acids. This property is not mediated by a β-glucosidase aggregating factor (BGAF) as in grasses (maize and sorghum). The role of these aggregates is discussed.
    Keywords β-glucosidase ; Sechium edule ; aggregating protein ; Cucurbitaceae ; Organic chemistry ; QD241-441
    Subject code 540
    Language English
    Publishing date 2020-04-01T00:00:00Z
    Publisher MDPI AG
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  9. Article ; Online: Purification and Partial Characterization of β-Glucosidase in Chayote (Sechium edule)

    Sergio Espíndola Mateos / Carlos Alberto Matías Cervantes / Edgar Zenteno / Marie-Christine Slomianny / Juan Alpuche / Pedro Hernández-Cruz / Ruth Martínez-Cruz / Maria del Socorro Pina Canseco / Eduardo Pérez-Campos / Manuel Sánchez Rubio / Laura Pérez-Campos Mayoral / Margarito Martínez-Cruz

    Molecules, Vol 20, Iss 10, Pp 19372-

    2015  Volume 19392

    Abstract: β-Glucosidase (EC 3.2.1.21) is a prominent member of the GH1 family of glycoside hydrolases. The properties of this β-glucosidase appear to include resistance to temperature, urea, and iodoacetamide, and it is activated by 2-ME, similar to other members. ...

    Abstract β-Glucosidase (EC 3.2.1.21) is a prominent member of the GH1 family of glycoside hydrolases. The properties of this β-glucosidase appear to include resistance to temperature, urea, and iodoacetamide, and it is activated by 2-ME, similar to other members. β-Glucosidase from chayote (Sechium edule) was purified by ionic-interchange chromatography and molecular exclusion chromatography. Peptides detected by LC-ESI-MS/MS were compared with other β-glucosidases using the BLAST program. This enzyme is a 116 kDa protein composed of two sub-units of 58 kDa and shows homology with Cucumis sativus β-glucosidase (NCBI reference sequence XP_004154617.1), in which seven peptides were found with relative masses ranging from 874.3643 to 1587.8297. The stability of β-glucosidase depends on an initial concentration of 0.2 mg/mL of protein at pH 5.0 which decreases by 33% in a period of 30 h, and then stabilizes and is active for the next 5 days (pH 4.0 gives similar results). One hundred μg/mL β-D-glucose inhibited β-glucosidase activity by more than 50%. The enzyme had a Km of 4.88 mM with p-NPG and a Kcat of 10,000 min−1. The optimal conditions for the enzyme require a pH of 4.0 and a temperature of 50 °C.
    Keywords β-glucosidase ; Cucurbitaceae ; Sechium edule ; glycosyl hydrolases ; Organic chemistry ; QD241-441
    Language English
    Publishing date 2015-10-01T00:00:00Z
    Publisher MDPI AG
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  10. Article ; Online: Protein C activation peptide inhibits the expression of ICAM-1, VCAM-1, and interleukin-8 induced by TNF-a in human dermal microvascular endothelial cells Protein C activation peptide inhibits the expression of ICAM-1, VCAM-1, and interleukin-8 induced by TNF-a in human dermal microvascular endothelial cells

    María Del Socorro Pina-Canseco / Araceli Páez-Arenas / Felipe Massó / Eduardo Pérez-Campos / Ruth Martínez-Cruz / Pedro Hernández-Cruz / Abraham Majluf-Cruz / Margarito Martínez-Cruz / Laura Pérez-Campos Mayoral / Alma Dolores Pérez-Santiago / Edgar Zenteno

    Folia Histochemica et Cytobiologica, Vol 50, Iss 3, Pp 407-

    2012  Volume 413

    Abstract: Activated protein C (APC) is generated from the cleavage of protein C by thrombin coupled to thrombomodulin and, subsequently, is released as protein C activation peptide (papC). The aim of this study was to evaluate the effect of papC on human dermal ... ...

    Abstract Activated protein C (APC) is generated from the cleavage of protein C by thrombin coupled to thrombomodulin and, subsequently, is released as protein C activation peptide (papC). The aim of this study was to evaluate the effect of papC on human dermal microvascular endothelial cells (HMEC-1), activated with 5 ng/ /mL TNF-a. Flow cytometry showed that papC inhibited the expression of VCAM-1 and ICAM-1, after activation with TNF-a. Similarly, RT-PCR analysis revealed that 2 and 4 pM papC inhibited the expression of VCAM-1 and IL-8 mRNA in TNF-a-treated HMEC-1. In addition, the expression of endothelial nitric oxide synthase (eNOS) increased in HMEC-1 treated with papC, compared to those without treatment. Furthermore, Jurkat cell adhesion to HMEC-1 induced by TNF-a was significantly inhibited after the addition of papC, compared to HMEC-1 without papC (p = 0.03). Finally, a control peptide analog to papC showed no effect on the expression of ICAM and VCAM on the surface of HMEC-1. In conclusion, our results suggest that papC exerts antiinflammatory effects on endothelial cells. Activated protein C (APC) is generated from the cleavage of protein C by thrombin coupled to thrombomodulin and, subsequently, is released as protein C activation peptide (papC). The aim of this study was to evaluate the effect of papC on human dermal microvascular endothelial cells (HMEC-1), activated with 5 ng/ /mL TNF-a. Flow cytometry showed that papC inhibited the expression of VCAM-1 and ICAM-1, after activation with TNF-a. Similarly, RT-PCR analysis revealed that 2 and 4 pM papC inhibited the expression of VCAM-1 and IL-8 mRNA in TNF-a-treated HMEC-1. In addition, the expression of endothelial nitric oxide synthase (eNOS) increased in HMEC-1 treated with papC, compared to those without treatment. Furthermore, Jurkat cell adhesion to HMEC-1 induced by TNF-a was significantly inhibited after the addition of papC, compared to HMEC-1 without papC (p = 0.03). Finally, a control peptide analog to papC showed no effect on the expression of ICAM and VCAM on the surface of HMEC-1. In conclusion, our results suggest that papC exerts antiinflammatory effects on endothelial cells.
    Keywords Biology (General) ; QH301-705.5 ; Science ; Q ; DOAJ:Biology ; DOAJ:Biology and Life Sciences
    Subject code 616
    Language English
    Publishing date 2012-10-01T00:00:00Z
    Publisher Polish Histochemical and Cytochemical Society
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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