Publications by authors named "Norma Segovia-Gamboa"

Nurr1 is a member of the orphan nuclear receptor family NR4A (nuclear receptor subfamily 4 group A) that modulates inflammation in several cell lineages, both positively and negatively. Macrophages are key regulators of inflammatory responses, yet information about the role of Nurr1 in human macrophages is scarce. Here we examined Nurr1 expression and activity in steady state and activated human macrophages.

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Article Synopsis
  • Nur77 is an orphan nuclear receptor that regulates various cellular functions including inflammation and immune responses in macrophages.
  • Its expression is significantly higher in anti-inflammatory macrophages (M-MDMs) than in pro-inflammatory ones (GM-MDMs), and stimulation with specific ligands can enhance its activity.
  • Nur77 activation reduces the production of pro-inflammatory cytokines while increasing anti-inflammatory cytokine IL-10, indicating its role in modulating the inflammatory response based on the macrophage type.
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Article Synopsis
  • Obesity triggers inflammation in the body by activating specific immune cells called adipose tissue macrophages (ATMs), shifting their types from beneficial to harmful.
  • In healthy individuals, ATMs in fat tissue generally promote tissue health (M2 type), but in obese people, there’s an increase in inflammatory ATMs (M1 type), especially in subcutaneous fat (SAT).
  • The study identified key markers for these macrophage types and found that while the overall count of beneficial ATMs increased in SAT of obese individuals, changes in visceral fat (VAT) were more complex, with a mix of both harmful and helpful macrophages present.
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Aims: To assess the prevalence of autoantibodies (Aab) to insulin (IAA), glutamic acid decarboxylase 65 (GADA) and insulinoma antigen 2 (IA-2A), as well as human leukocyte antigen (HLA) class II alleles, in first degree relatives (FDR) of Mexican patients with type 1 diabetes (T1D), and to explore whether these parameters mirror the low incidence of T1D in the Mexican population.

Methods: Aab titers were determined by ELISA in 425 FDR, 234 siblings, 40 offspring and 151 parents of 197 patients with T1D. Typing of HLA-DR and -DQ alleles was performed in 41 Aab-positive FDR using polymerase chain reaction with allele-specific oligotyping.

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Tolerogenic dendritic cells (tDC) constitute a promising therapy for autoimmune diseases, since they can anergize T lymphocytes recognizing self-antigens. Patients with type 1 diabetes mellitus (T1D) have autoreactive T cells against pancreatic islet antigens (insulin, glutamic acid decarboxylase 65 -GAD65-). We aimed to determine the ability of tDC derived from T1D patients to inactivate their insulin- and GAD65-reactive T cells.

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The free living amoeba Naegleria fowleri is pathogenic to humans but also to other mammalians. These amoebae may invade the nasal mucosa and migrate into the brain causing cerebral hemorrhagic necrosis, a rapidly fatal infection. Knowledge of the cytolytic mechanism involved in the destruction of brain tissues by Naegleria trophozoites is limited.

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Cysts of Naegleria fowleri present an external single-layered cyst wall. To date, little information exists on the biochemical components of this cyst wall. Knowledge of the cyst wall composition is important to understand its resistance capacity under adverse environmental conditions.

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The study of the encystation process of Entamoeba histolytica has been hampered by the lack of experimental means of inducing mature cysts in vitro. Previously we have found that cytoplasmic vesicles similar to the encystation vesicles of Entamoeba invadens are present in E. histolytica trophozoites only in amebas recovered from experimental amebic liver abscesses.

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The reptilian parasite Entamoeba invadens is accepted as a model for the study of the Entamoeba encystation process. Here we describe the production and characterization of a mAb (B4F2), generated against a component of the E. invadens cyst wall.

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