Kalia N. Aguera

ORCID: 0000-0001-9701-7682
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Research Areas
  • Platelet Disorders and Treatments
  • Angiogenesis and VEGF in Cancer
  • Kruppel-like factors research
  • Cell Adhesion Molecules Research
  • Blood Coagulation and Thrombosis Mechanisms
  • Chemokine receptors and signaling
  • Chronic Myeloid Leukemia Treatments
  • Barrier Structure and Function Studies
  • Vascular Malformations Diagnosis and Treatment
  • Vascular Malformations and Hemangiomas
  • Cancer Treatment and Pharmacology
  • Cancer Cells and Metastasis
  • Microtubule and mitosis dynamics
  • Hippo pathway signaling and YAP/TAZ

University of South Florida
2019-2024

Objective: We sought to identify and investigate the functional role of major endothelial cell (EC)-derived factors that control pericyte recruitment EC tubes pericyte-induced tube maturation during capillary network formation. Approach Results: PDGF (platelet-derived growth factor)-BB, PDGF-DD, ET (endothelin)-1, TGF (transforming factor)-β, HB-EGF (heparin-binding epidermal factor), as key individual combined regulators assembly around tubes. Using novel only assays, we demonstrate...

10.1161/atvbaha.120.314948 article EN Arteriosclerosis Thrombosis and Vascular Biology 2020-08-20

In this work, we examine the molecular basis for capillary tube regression and identify key proregressive factors, signaling pathways, pharmacological antagonists of process. Approach Results: We demonstrate that proinflammatory mediators, IL (interleukin)-1β, TNF (tumor necrosis factor) α, thrombin, singly in combination, are potent regulators vitro. These when added to endothelial cell-pericyte cocultures, led selective loss cell-lined networks, with retention proliferation pericytes...

10.1161/atvbaha.119.313536 article EN Arteriosclerosis Thrombosis and Vascular Biology 2019-12-19

Objective: In this work, we have sought to define growth factor requirements and the signaling basis for different stages of human vascular morphogenesis maturation. Approach Results: Using a serum-free model endothelial cell (EC) tube in 3-dimensional collagen matrices that depends on 5 combination, SCF (stem factor), IL (interleukin)-3, SDF (stromal-derived factor)-1α, FGF (fibroblast factor)-2, insulin (factors), demonstrate VEGF (vascular factor) pretreatment ECs 8 hours (ie, priming)...

10.1161/atvbaha.120.314517 article EN Arteriosclerosis Thrombosis and Vascular Biology 2020-10-22

Blood vessels in different vascular beds vary size, which is essential for their function and fluid flow along the network. Molecular mechanisms involved formation of a lumen appropriate or tubulogenesis, are still only partially understood. Src homology 2 domain containing E (She) protein was previously identified screen proteins that interact with Abelson (Abl)-kinase. However, its biological role has remained unknown. Here we demonstrate She Abl signaling regulate vessel size zebrafish...

10.1371/journal.pgen.1010851 article EN cc-by PLoS Genetics 2024-01-08

Objective: We sought to determine how endothelial cell (EC) expression of the activating k-Ras (kirsten rat sarcoma 2 viral oncogene homolog) mutation, k-RasV12, affects their ability form lumens and tubes interact with pericytes during capillary assembly Approach Results: Using defined bioassays where human ECs undergo observable tubulogenesis, sprouting behavior, pericyte recruitment EC-lined tubes, pericyte-induced EC basement membrane deposition, we assessed impact k-RasV12 on these...

10.1161/atvbaha.121.316798 article EN Arteriosclerosis Thrombosis and Vascular Biology 2021-12-09

Abstract Blood vessels in different vascular beds vary lumen diameter, which is essential for their function and fluid flow along the network. Molecular mechanisms involved formation of a appropriate size, or tubulogenesis, are still only partially understood. Src homology 2 domain containing E (She) protein was previously identified screen proteins that interact with Abelson (Abl)-kinase. However, its biological role has remained unknown. Here we demonstrate She Abl signaling regulate size...

10.1101/2023.07.03.547455 preprint EN cc-by bioRxiv (Cold Spring Harbor Laboratory) 2023-07-03
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