Publications by authors named "Jun-Young Hong"

The AC magnetic field response of the superparamagnetic nano-ferrofluid is an interplay between the Neel and Brownian relaxation processes and is generally quantified via the susceptibility measurements at high frequencies. The high frequency limit is dictated by these relaxation times which need to be shorter than the time scale of the time varying magnetic field for the nano-ferrofluid to be considered in an equilibrium state at each time instant. Even though the high frequency response of ferrofluid has been extensively investigated for frequencies up to GHz range by non-optical methods, harnessing dynamic response by optical means for AC magnetic field sensing in fiber-optic-based sensors-field remains unexplored.

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Metastasis is the leading cause of cancer-related mortality. Paneth cells provide stem cell niche factors in homeostatic conditions, but the underlying mechanisms of cancer stem cell niche development are unclear. Here, we report that Dickkopf-2 (DKK2) is essential for the generation of cancer cells with Paneth cell properties during colon cancer metastasis.

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Alzheimer's disease (AD) is a progressive neurodegenerative disease accompanied by neurotoxicity, excessive inflammation, and cognitive impairment. The peroxisome proliferator-activated receptor (PPAR) δ is a potential target for AD. However, its regulatory mechanisms and therapeutic potential in AD remain unclear.

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  • Pregnancy involves a unique immune situation where the mother's body must accept the semi-foreign fetus, which carries genes from the father.
  • Successful pregnancy relies on complex mechanisms that promote immune tolerance, such as the barrier of the placenta, regulatory immune cells, and specific biological responses that protect the fetus.
  • Understanding how the body maintains this tolerance not only sheds light on pregnancy health but may also lead to new cancer treatments and insights into complications that arise when this tolerance is disrupted.
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Diffuse large B-cell lymphomas (DLBCLs) are heterogeneous cancers that still require better and less toxic treatments. SIRT3, a member of the sirtuin family of NAD-dependent protein deacylase, is critical for DLBCL growth and survival. A mitochondria-targeted SIRT3 small-molecule inhibitor, YC8-02, exhibits promising activity against DLBCL.

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Metastasis is the leading cause of cancer-related mortality. Paneth cells provide stem cell niche factors in homeostatic conditions, but the underlying mechanisms of cancer stem cell niche development are unclear. Here we report that Dickkopf-2 (DKK2) is essential for the generation of cancer cells with Paneth cell properties during colon cancer metastasis.

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Sirt2 is a nicotinamide adenine dinucleotide (NAD)-dependent protein lysine deacylase that can remove both acetyl group and long-chain fatty acyl groups from lysine residues of many proteins. It was reported to affect inflammatory bowel disease (IBD) symptoms in a mouse model. However, conflicting roles were reported, with genetic knockout aggravating while pharmacological inhibition alleviating IBD symptoms.

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Early-life environmental exposures play a significant role in shaping long-lasting immune phenotypes and disease susceptibility. Nevertheless, comprehensive understanding of the developmental programming of immunity is limited. We propose that the vertebrate immune system contains durable programmable components established through early environmental interactions and maintained in a stable and homeostatic manner.

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  • The tradeoff between light absorption and charge transport in PbS colloidal quantum dot solar cells is addressed by integrating a Fabry-Perot resonator with a distributed Bragg reflector.
  • This combination enhances light absorption at specific wavelengths without increasing the thickness of the CQD film, resulting in a 54% boost in power conversion efficiency (PCE).
  • Additionally, the device maintains a balance between effective absorption of near-infrared light and visible light transparency, achieving a 24% increase in PCE while preserving average visible transmittance.
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  • * Sirtuin 3 (SIRT3), a regulator of oxidative phosphorylation (OXPHOS), is crucial for the survival of human LSC but not for normal blood stem cells, indicating its potential as a treatment target.
  • * By studying LSC's response to SIRT3 inhibition, researchers found ways to enhance LSC death, such as disrupting cholesterol balance and combining SIRT3 inhibition with a specific cancer drug, suggesting new treatment avenues for AML.
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  • The HLA-C*01:242 and HLA-C*01:02:01:01 alleles are variations of the HLA-C gene.
  • They differ from each other by just one nucleotide.
  • This difference occurs specifically at codon 281 of the gene.
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The HLA-DPA1*02:89 allele differs from HLA-DPA1*02:02:02:01 allele by a single nucleotide in codon 224.

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  • * It differs from another variant, HLA-DQA1*01:03:01:01, by just one nucleotide change.
  • * This change occurs specifically at codon -8 of the gene.
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Early-life environmental factors can have persistent effects on physiological functions by altering developmental procedures in various organisms. Recent experimental and epidemiological studies now further support the idea that developmental programming is also present in mammals, including humans, influencing long-term health. Although the mechanism of programming is still largely under investigation, the role of endocrine glucocorticoids in developmental programming is gaining interest.

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IgE mediates allergic responses by coating mast cell or basophil surfaces and inducing degranulation upon binding a specific allergen. IgE can also be spontaneously produced in the absence of foreign allergens; yet the origin, regulation, and functions of such "natural" IgE still remain largely unknown. Here, we find that glucocorticoids enhance the production of IgE in B cells both in vivo and ex vivo without antigenic challenge.

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The HLA-DRB4*01:162N allele differs from HLA-DRB4*01:03:01:01 allele by a single nucleotide in codon 131.

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  • Recent research shows that the immune system is involved in more than just fighting infections; it also influences various bodily functions even in the absence of pathogens.
  • There is a significant connection between immunity and metabolism, where immune signals can impact metabolic processes and vice versa.
  • The review aims to summarize these findings on how immunity and metabolism interact and explore the underlying biological principles of this relationship.
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  • The HLA-B*56:01:18 allele is a variation of the HLA-B*56:01:01:01 allele.
  • The difference between these two alleles is caused by a single nucleotide change.
  • This change occurs specifically at codon 326.3 in the gene sequence.
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  • The HLA-A*26:01:75 allele is a variant of the HLA-A*26:01:01:01 allele.
  • The difference between these two alleles is caused by a single nucleotide change.
  • This specific change occurs at codon -10.3.
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  • A new method for producing histone H2B through semisynthesis using an engineered sortase transpeptidase is introduced.
  • The study involves modifying the N-terminal tail of histone H2B with different chemical groups (acetyl, lactyl, β-hydroxybutyryl) and incorporating these modified histones into nucleosomes.
  • The modified histones were tested as substrates for histone deacetylase complexes and sirtuins, revealing varied rates and site-specific activities that indicate their unique roles in regulating chromatin structure and epigenetic processes.
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  • - Myristoylation on lysine, unlike the well-known modification on glycine, plays a crucial but poorly understood role in protein function and localization, specifically for the protein gravin-α.
  • - Gravin-α is myristoylated on two lysine residues, which allows it to interact with histone deacetylase 11 (HDAC11) that can remove these modifications, impacting signaling pathways in adipocytes.
  • - This lysine myristoylation is essential for the proper functioning of β-adrenergic receptors, leading to the activation of PKA and promoting thermogenic gene expression, suggesting a potential therapeutic target in obesity management by inhibiting HDAC11.
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  • Diffuse large B-cell lymphomas (DLBCL) rely on a metabolic process regulated by mitochondrial SIRT3, and its depletion triggers cell death through reduced levels of ATF4.
  • The study indicates that ATF4 production is decreased in SIRT3-deficient cells, which affects amino acid metabolism and survival of DLBCL cells.
  • By targeting the SIRT3-ATF4 pathway, researchers suggest potential new therapeutic strategies to enhance the effectiveness of SIRT3 inhibitors in treating DLBCL.
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The lipid raft-resident protein, MAL2, has been implicated as contributing to the pathogenesis of several malignancies, including breast cancer, but the underlying mechanism for its effects on tumorigenesis is unknown. Here, we show that MAL2-mediated lipid raft formation leads to HER2 plasma membrane retention and enhanced HER2 signaling in breast cancer cells. We demonstrate physical interactions between HER2 and MAL2 in lipid rafts using proximity ligation assays.

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  • The HLA-DQA1*03:02:03 allele has a small genetic variation compared to the HLA-DQA1*03:02:01:01 allele.
  • This difference is caused by a single nucleotide change in codon 42 of the gene.
  • Such variations can affect how the immune system recognizes and responds to different antigens.
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  • - Sirtuins are a group of seven proteins (SIRT1-7) in humans that utilize NAD to modify protein lysine residues, influencing various biological processes like cell growth, metabolism, and movement.
  • - These proteins play distinct roles and are involved in the regulation of various diseases, such as cancer, neurodegeneration, and metabolic disorders, making them crucial for our understanding of human health.
  • - The review discusses how genetic and drug-based approaches can influence sirtuins, highlighting the growing interest in developing treatments that target these proteins to address their role in diseases.
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