Publications by authors named "Jonathan L Catrow"

Lactate is the highest turnover circulating metabolite in mammals. While traditionally viewed as a waste product, lactate is an important energy source for many organs, but first must be oxidized to pyruvate for entry into the tricarboxylic acid cycle (TCA cycle). This reaction is thought to occur in the cytosol, with pyruvate subsequently transported into mitochondria via the mitochondrial pyruvate carrier (MPC).

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Article Synopsis
  • Abcb10 is a mitochondrial protein crucial for transporting biliverdin, which is essential for the formation of hemoglobin in red blood cells.
  • Deleting Abcb10 in both mouse and human erythroid cells led to failure in hemoglobinization, lower heme levels, and impaired arginine metabolism, resulting in decreased cell proliferation.
  • The study highlights how Abcb10 loss activates stress responses that hinder protein synthesis, ultimately affecting nutrient sensing and leading to further reductions in cell growth and hemoglobin production.
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Potential anti-inflammatory and anticarcinogenic effects of aspirin (ASA) may be suitable for melanoma chemoprevention, but defining biomarkers in relevant target tissues is prerequisite to performing randomized controlled chemoprevention trials. We conducted open-label studies with ASA in 53 human subjects with melanocytic nevi at increased risk for melanoma. In a pilot study, 12 subjects received a single dose (325 mg) of ASA; metabolites salicylate, salicylurate, and gentisic acid were detected in plasma after 4-8 h, and prostaglandin E2 (PGE) was suppressed in both plasma and nevi for up to 24 h.

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Macrophages are susceptible to human immunodeficiency virus type 1 (HIV-1) infection despite abundant expression of antiviral proteins. Perhaps the most important antiviral protein is the restriction factor sterile alpha motif domain and histidine/aspartic acid domain-containing protein 1 (SAMHD1). We investigated the role of SAMHD1 and its phospho-dependent regulation in the context of HIV-1 infection in primary human monocyte-derived macrophages and the ability of various interferons (IFNs) and pharmacologic agents to modulate SAMHD1.

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