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Eliseo A. Eugenin

Researcher at University of Texas Medical Branch

Publications -  149
Citations -  8873

Eliseo A. Eugenin is an academic researcher from University of Texas Medical Branch. The author has contributed to research in topics: Microglia & Connexin. The author has an hindex of 47, co-authored 135 publications receiving 7396 citations. Previous affiliations of Eliseo A. Eugenin include Rutgers University & Pontifical Catholic University of Chile.

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Metabolic inhibition induces opening of unapposed connexin 43 gap junction hemichannels and reduces gap junctional communication in cortical astrocytes in culture

TL;DR: Subjecting rat and mouse cortical astrocytes to “chemical ischemia” by inhibition of glycolytic and oxidative metabolism induced permeabilization of cells to Lucifer yellow and ethidium bromide before loss of membrane integrity determined by dextran uptake and lactate dehydrogenase release, suggesting that dye uptake is mediated by Cx43 hemichannels.
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CCL2/monocyte chemoattractant protein-1 mediates enhanced transmigration of human immunodeficiency virus (HIV)-infected leukocytes across the blood-brain barrier : A potential mechanism of HIV-CNS invasion and NeuroAIDS

TL;DR: It is demonstrated that HIV infection of human leukocytes results in their increased transmigration across the tissue culture model of the human BBB in response to the chemokine CCL2, as well as in disruption of the BBB, as evidenced by enhanced permeability, reduction of tight junction proteins, and expression of matrix metalloproteinases (MMP)-2 and MMP-9.
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Microglial stimulation of glioblastoma invasion involves epidermal growth factor receptor (EGFR) and colony stimulating factor 1 receptor (CSF-1R) signaling.

TL;DR: Analysis of how microglia, the resident macrophages of the brain, stimulate glioblastoma cell invasion and interactions mediated by EGF and CSF-1 can enhance gliOBlastoma invasion demonstrate the possibility of inhibiting gliobeastsoma invasion by targeting gliablastoma-associated microglial enhancement via inhibition of the CSf-1R.
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MCP-1 (CCL2) protects human neurons and astrocytes from NMDA or HIV-tat-induced apoptosis.

TL;DR: Monocyte chemoattractant protein‐1 (MCP‐1 or CCL2) and regulated upon activation normal T cell expressed and secreted (RANTES) were found to protect mixed cultures of human neurons and astrocytes from tat or NMDA‐induced apoptosis, indicating that MCP‐ 1 may play a novel role as a protective agent against the toxic effects of glutamate and tat.
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Tunneling nanotubes (TNT) are induced by HIV-infection of macrophages: a potential mechanism for intercellular HIV trafficking.

TL;DR: It is proposed that HIV "highjacks" TNT communication to spread HIV through an intercellular route between communicated cells, contributing to the pathogenesis of AIDS.