Publications by authors named "Mahalia Huba"

Introduction: Nonbacterial Thrombotic Endocarditis (NBTE) is a rare condition characterized by aseptic vegetations of the heart valves, predisposing to valvular dysfunction and end-organ infarction. Lung Cancer (LC) is amongst the most common malignancies associated with NBTE.

Methods: PubMed/MEDLINE was searched from database inception until January 2024, pairing "Non-Bacterial Thrombotic Endocarditis (NBTE) and related terms with "Lung Cancer"( LC).

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Background: Distinct endothelial cell cycle states (early G1 versus late G1) provide different "windows of opportunity" to enable the differential expression of genes that regulate venous versus arterial specification, respectively. Endothelial cell cycle control and arteriovenous identities are disrupted in vascular malformations including arteriovenous shunts, the hallmark of hereditary hemorrhagic telangiectasia (HHT). To date, the mechanistic link between endothelial cell cycle regulation and the development of arteriovenous malformations (AVMs) in HHT is not known.

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Background: Clonal hematopoiesis (CH), which results from an array of nonmalignant driver gene mutations, can lead to altered immune cell function and chronic disease, and has been associated with worse outcomes in patients with heart failure (HF) with reduced ejection fraction. However, the role of CH in the prognosis of HF with preserved ejection fraction (HFpEF) has been understudied. This study aimed to characterize CH in patients with HFpEF and elucidate its causal role in a murine model.

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The subventricular zone (SVZ) is the largest neural stem cell (NSC) niche in the adult brain; herein, the blood-brain barrier is leaky, allowing direct interactions between NSCs and endothelial cells (ECs). Mechanisms by which direct NSC-EC interactions in the adult SVZ control NSC behavior are unclear. We found that Cx43 is highly expressed by SVZ NSCs and ECs, and its deletion in either leads to increased NSC proliferation and neuroblast generation, suggesting that Cx43-mediated NSC-EC interactions maintain NSC quiescence.

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Article Synopsis
  • Endothelial cells differentiate into arterial or venous types during blood vessel development, crucial for nutrient and waste transport in tissues.
  • The study uses specific mouse models to reveal that venous endothelial cells are primarily in an early G1 state with BMP signaling, while arterial cells are in a late G1 state with TGF-β signaling.
  • They found that these cell cycle stages are critical for the expression of venous and arterial genes, and that preventing cell cycle progression can fix defects in arterial-venous specification.
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