Publications by authors named "Laura D Harmacek"

The contribution and regulation of various CD4+ T cell lineages that occur with remitting vs progressive courses in sarcoidosis are poorly understood. We developed a multiparameter flow cytometry panel to sort these CD4+ T cell lineages followed by measurement of their functional potential using RNA-sequencing analysis at six-month intervals across multiple study sites. To obtain good quality RNA for sequencing, we relied on chemokine receptor expression to identify and sort lineages.

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Cystic fibrosis (CF) is an inherited disorder caused by biallelic mutations of the CF transmembrane conductance regulator (CFTR) gene. Converging evidence suggests that CF carriers with only 1 defective CFTR copy are at increased risk for CF-related conditions and pulmonary infections, but the molecular mechanisms underpinning this effect remain unknown. We performed transcriptomic profiling of peripheral blood mononuclear cells (PBMCs) of CF child-parent trios (proband, father, and mother) and healthy control (HC) PBMCs or THP-1 cells incubated with the plasma of these participants.

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Introduction: Sarcoidosis is a multiorgan granulomatous disorder thought to be triggered and influenced by gene-environment interactions. Sarcoidosis affects 45-300/100 000 individuals in the USA and has an increasing mortality rate. The greatest gap in knowledge about sarcoidosis pathobiology is a lack of understanding about the underlying immunological mechanisms driving progressive pulmonary disease.

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Article Synopsis
  • The study investigates the potential of PBMC expression profiles to predict disease progression in patients with chronic hypersensitivity pneumonitis (CHP) alongside traditional clinical assessments.
  • RNA-seq analysis revealed 74 transcripts that differentiate between patients with and without disease progression based on specific lung function declines and increased fibrosis visible on chest CTs.
  • Moreover, classification models that integrate gene expression data and clinical factors provide significantly better predictions of disease progression than models using only clinical data.
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Article Synopsis
  • Conventional methods for studying chromatin accessibility, like MNase-seq, DNase-seq, and ChIP-seq, require large cell quantities, making it challenging to directly analyze CD4+ T cells from individual mice.
  • A new method is proposed that uses cytokine reporter mice combined with ATAC-seq, which allows researchers to study locus accessibility in small populations of cytokine-expressing CD4+ T cells.
  • This method successfully identifies transposase integration in IL-4 and IFN-γ expressing CD4+ T cells from lungs and lymph nodes after helminth infection, highlighting its effectiveness for epigenetic research.
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SPPA1 is a protease in the plastids of plants, located in non-appressed thylakoid regions. In this study, T-DNA insertion mutants of the single-copy SPPA1 gene in Arabidopsis thaliana (At1g73990) were examined. Mutation of SPPA1 had no effect on the growth and development of plants under moderate, non-stressful conditions.

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Integrins are important cell surface receptors that transmit bidirectional signals across the membrane. It has been shown that a conformational change of the integrin beta-subunit headpiece (i.e.

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