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1.
Diabetes ; 69(11): 2310-2323, 2020 11.
Artículo en Inglés | MEDLINE | ID: mdl-32732304

RESUMEN

Elevated expression of E2F1 in adipocyte fraction of human visceral adipose tissue (hVAT) associates with a poor cardiometabolic profile. We hypothesized that beyond directly activating autophagy and MAP3K5 (ASK)-MAP kinase signaling, E2F1 governs a distinct transcriptome that contributes to adipose tissue and metabolic dysfunction in obesity. We performed RNA sequencing of hVAT samples from age-, sex-, and BMI-matched patients, all obese, whose visceral E2F1 protein expression was either high (E2F1high) or low (E2F1low). Tumor necrosis factor superfamily (TNFSF) members, including TRAIL (TNFSF10), TL1A (TNFSF15), and their receptors, were enriched in E2F1high While TRAIL was equally expressed in adipocytes and stromal vascular fraction (SVF), TL1A was mainly expressed in SVF, and TRAIL-induced TL1A was attributed to CD4+ and CD8+ subclasses of hVAT T cells. In human adipocytes, TL1A enhanced basal and impaired insulin-inhibitable lipolysis and altered adipokine secretion, and in human macrophages it induced foam cell biogenesis and M1 polarization. Two independent human cohorts confirmed associations between TL1A and TRAIL expression in hVAT and higher leptin and IL6 serum concentrations, diabetes status, and hVAT-macrophage lipid content. Jointly, we propose an intra-adipose tissue E2F1-associated TNFSF paracrine loop engaging lymphocytes, macrophages, and adipocytes, ultimately contributing to adipose tissue dysfunction in obesity.


Asunto(s)
Adipocitos/fisiología , Factor de Transcripción E2F1/metabolismo , Linfocitos/fisiología , Macrófagos/fisiología , Ligando Inductor de Apoptosis Relacionado con TNF/metabolismo , Miembro 15 de la Superfamilia de Ligandos de Factores de Necrosis Tumoral/metabolismo , Tejido Adiposo/fisiología , Adolescente , Adulto , Anciano , Anciano de 80 o más Años , Células Cultivadas , Técnicas de Cocultivo , Factor de Transcripción E2F1/genética , Femenino , Regulación de la Expresión Génica , Humanos , Masculino , Persona de Mediana Edad , Comunicación Paracrina , Ligando Inductor de Apoptosis Relacionado con TNF/genética , Miembro 15 de la Superfamilia de Ligandos de Factores de Necrosis Tumoral/genética , Adulto Joven
2.
J Matern Fetal Neonatal Med ; 27(12): 1189-94, 2014 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-24111719

RESUMEN

OBJECTIVE: To examine if, as in obesity, pregnancies complicated by gestational diabetes mellitus (GDM) exhibit increased macrophage infiltration and activated MAP-kinases in omental adipose tissue. METHODS: Paired omental (OM) and abdominal subcutaneous (SC) fat samples were collected from 11 GDM and 20 normal pregnancies during cesarean delivery. Tissues were stained to detect macrophages, and analyzed to assess MAP-kinases. RESULTS: OM had higher macrophage counts than SC in GDM (6.10 ± 2.20 versus 2.53 ± 1.45, p = 0.04), but not in normal pregnancies (p = 0.346). GDM pregnancies had more macrophages than normal pregnancies in OM (6.10 ± 2.20 versus 1.29 ± 0.55, p = 0.01), while only a trend was observed in SC fat (p = 0.08). Significant correlation (R = 0.619, p = 0.005) was observed between OM-macrophage infiltration and insulin resistance. Using multivariate analysis, only obesity independently associated with GDM. Expression of total p38MAP-kinase was higher in OM versus SC in both normal and GDM pregnancies, without significant differences between these groups. However, expression of activated p-p38MAP-kinase, and its upstream kinase MKK4, was comparable between fat depots. CONCLUSION: GDM pregnancies demonstrate increased macrophage infiltration to OM fat, correlating with higher insulin resistance. As in non-pregnant-patients obesity and OM macrophage infiltration may be on the same causal pathway, leading to GDM. Yet, this occurs without activation of p38MAP-kinase signaling.


Asunto(s)
Grasa Abdominal , Movimiento Celular , Diabetes Gestacional , Macrófagos/fisiología , Estrés Fisiológico , Grasa Subcutánea , Grasa Abdominal/inmunología , Grasa Abdominal/metabolismo , Adulto , Estudios de Casos y Controles , Movimiento Celular/inmunología , Diabetes Gestacional/inmunología , Diabetes Gestacional/metabolismo , Femenino , Humanos , MAP Quinasa Quinasa 4/metabolismo , Epiplón , Embarazo , Transducción de Señal , Grasa Subcutánea/inmunología , Grasa Subcutánea/metabolismo , Proteínas Quinasas p38 Activadas por Mitógenos/metabolismo
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