Alternative splicing of SMPD1 in human sepsis.

PLoS One

Integrated Research and Treatment Center, Center for Sepsis Control and Care (CSCC), Jena University Hospital, Jena, Germany; Department of Anesthesiology and Intensive Care Therapy, Jena University Hospital, Jena, Germany.

Published: April 2016

AI Article Synopsis

  • Acid sphingomyelinase (ASM) plays a key role in regulating immune responses and organ failure in critically ill patients.
  • Alternative splicing of the ASM gene (SMPD1) shows distinct patterns in patients with systemic inflammatory response syndrome and severe sepsis, compared to healthy individuals.
  • These splicing variations could help deepen our understanding of the mechanisms involved in human sepsis.

Article Abstract

Acid sphingomyelinase (ASM or sphingomyelin phosphodiesterase, SMPD) activity engages a critical role for regulation of immune response and development of organ failure in critically ill patients. Beside genetic variation in the human gene encoding ASM (SMPD1), alternative splicing of the mRNA is involved in regulation of enzymatic activity. Here we show that the patterns of alternatively spliced SMPD1 transcripts are significantly different in patients with systemic inflammatory response syndrome and severe sepsis/septic shock compared to control subjects allowing discrimination of respective disease entity. The different splicing patterns might contribute to the better understanding of the pathophysiology of human sepsis.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4405572PMC
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0124503PLOS

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