Induction of hypoxia-inducible factor-1alpha and activation of caspase-3 in hypoxia-reoxygenated bone marrow stroma is negatively regulated by the delayed production of substance P

J Immunol. 2001 Oct 15;167(8):4600-8. doi: 10.4049/jimmunol.167.8.4600.

Abstract

The bone marrow (BM), which is the major site of immune cell development in the adult, responds to different stimuli such as inflammation and hemorrhagic shock. Substance P (SP) is the major peptide encoded by the immune/hemopoietic modulator gene, preprotachykinin-1 (PPT-I). Differential gene expression using a microarray showed that SP reduced hypoxia-inducible factor-1alpha (HIF-1alpha) mRNA levels in BM stroma. Because long-term hypoxia induced the expression of PPT-I in BM mononuclear cells, we used timeline studies to determine whether PPT-I is central to the biologic responses of BM stroma subjected to 30-min hypoxia (pO(2) = 35 mm Hg) followed by reoxygenation. HIF-1alpha mRNA and protein levels were increased up to 12 h. At this time, beta-PPT-I mRNA was detected with the release of SP at 16 h. SP release correlated with down-regulation of HIF-1alpha to baseline. A direct role for SP in HIF-1alpha expression was demonstrated as follows: 1) transient knockout of beta-PPT-I showed an increase in HIF-1alpha expression up to 48 h of reoxygenation; and 2) HIF-1alpha expression remained baseline during reoxygenation when stroma was subjected to hypoxia in the presence of SP. Reoxygenation activated the PPT-I promoter with concomitant nuclear translocation of HIF-1alpha that can bind to the respective consensus sequences within the PPT-I promoter. SP reversed active caspase-3, an indicator of apoptosis and erythropoiesis, to homeostasis level after reoxygenation of hypoxic stroma. The results show that during reoxgenation the PPT-I gene acts as a negative regulator on the expression of HIF-1alpha and active caspase-3 in BM stroma subjected to reoxygenation.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • 5' Untranslated Regions
  • Adult
  • Bone Marrow / metabolism*
  • Caspase 3
  • Caspases / metabolism*
  • Cell Hypoxia
  • Enzyme Activation
  • Gene Expression Regulation
  • Hematopoiesis
  • Humans
  • Hypoxia-Inducible Factor 1, alpha Subunit
  • Oxygen / pharmacology*
  • Promoter Regions, Genetic
  • Protein Precursors / genetics
  • Stromal Cells / metabolism
  • Substance P / biosynthesis*
  • Tachykinins / genetics
  • Transcription Factors / biosynthesis*

Substances

  • 5' Untranslated Regions
  • HIF1A protein, human
  • Hypoxia-Inducible Factor 1, alpha Subunit
  • Protein Precursors
  • Tachykinins
  • Transcription Factors
  • preprotachykinin
  • Substance P
  • CASP3 protein, human
  • Caspase 3
  • Caspases
  • Oxygen