Pam3CSK4 and LTA-TLRs ligands associated with microdomains induce IL8 production in human adrenocortical cancer cells

Publikation: Beitrag in FachzeitschriftForschungsartikelBeigetragenBegutachtung

Beitragende

  • W. Kanczkowski - , Medizinische Klinik und Poliklinik 3 (Autor:in)
  • H. Morawietz - , Medizinische Klinik und Poliklinik 3 (Autor:in)
  • C. C. Ziegler - , Medizinische Klinik und Poliklinik 3 (Autor:in)
  • R. H. Funk - , Institut für Anatomie (Autor:in)
  • C. Schmitz - , Universität Regensburg (Autor:in)
  • K. Zacharowski - , University of Bristol (Autor:in)
  • C. E. Mohn - , Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET) (Autor:in)
  • M. Ehrhart-Bornstein - , Medizinische Klinik und Poliklinik 3 (Autor:in)
  • S. R. Bornstein - , Medizinische Klinik und Poliklinik 3 (Autor:in)

Abstract

Bacterially derived ligands, Pam3CSK4 and LPS, can directly impact adrenal glands steroidogenesis through microdomain-related TLR1/2 and 4, respectively, and indirectly via immune cell-derived cytokines. The bilateral immunoadrenal relationship plays an important role in the proper functioning of both systems. CXC chemokine-dependent immune cell infiltration into adrenocortical carcinomas (ACC), which correlates with poor prognosis, is a common phenomenon. Recently, IL8 was identified in ACC and NCI-H295R cells, and was found to contribute to ACC tumour growth. The aim of this study was to clarify the role of different TLR ligands in IL8 production in NCI-H295R cells. This is the first study to demonstrate the expression of several TLRs including TLR1, 3, 6, 7 and 9 in human adrenocortical cells by using the RT-PCR approach. Only stimulation with TLR1/6 together with TLR2 ligands resulted in IL8 peptide and mRNA induction in a dose and time-dependent manner. Our data suggest that gram-positive bacteria-related TLR1/2/6 ligands might contribute to adrenal gland tumorigenesis via IL8 production.

Details

OriginalspracheEnglisch
Seiten (von - bis)457-460
Seitenumfang4
FachzeitschriftHormone and metabolic research
Jahrgang39
Ausgabenummer6
PublikationsstatusVeröffentlicht - Juni 2007
Peer-Review-StatusJa

Externe IDs

PubMed 17578764
ORCID /0000-0001-9360-9736/work/164198491

Schlagworte

Schlagwörter

  • Bacterial ligands, CXC chemokines, Microdomains, NCI-H295R, TLR1/2, Tumorigenesis