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Procalcitonin and CGRP-I mRNA expression in various human tissues

  • Stefan Russwurm
  • , Ilmars Stonans*
  • , Elita Stonane
  • , Matthias Wiederhold
  • , Andrea Luber
  • , Peter F. Zipfel
  • , Hans Peter Deigner
  • , Konrad Reinhart
  • *Šī darba korespondējošais autors
  • Friedrich Schiller University Jena
  • Endress+Hauser AG

Zinātniskās darbības rezultāts: Devums žurnālamZinātniskais raksts (žurnālā)koleģiāli recenzēts

86 Atsauces (Scopus)

Kopsavilkums

Procalcitonin (PCT) is a highly sensitive and specific marker of systemic bacterial infection and sepsis. In contrast to its diagnostic significance, the cellular sources of plasma procalcitonin remain to be clarified. Two forms of PCT mRNAs originate from calcitonin/calcitonin gene-related peptide gene (CALC-I gene) along with mRNA for calcitonin gene-related peptide-I (CGRP-I). Reverse transcription polymerase chain reaction with newly designed primers detecting different PCT mRNAs and CGRP-I mRNA was used to identify tissues that might contribute to PCT production. Our study indicates that a variety of human tissues (13 of the 16 analyzed overall) express PCT-I, PCT-II, and/or CGRP-I mRNAs, with the highest levels detected for liver, testis, lung, prostate, kidney, and small intestine. Various tissues differ in the proportions of PCT-I, PCT-II, and CGRP-I mRNA expression levels. Thus we demonstrate the complexity of tissue-specific regulation of CALC-I gene expression and suppose a variety of tissues as a potential source of CALC-I-encoded peptides.

OriģinālvalodaAngļu
Lapas (no-līdz)109-112
Lapu skaits4
ŽurnālsShock
Sējums16
Izdevuma numurs2
DOIs
Publikācijas statussPublicēts - aug. 2001
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