[HTML][HTML] The endothelial cell receptor GRP78 is required for mucormycosis pathogenesis in diabetic mice

M Liu, B Spellberg, QT Phan, Y Fu, Y Fu… - The Journal of …, 2010 - Am Soc Clin Investig
M Liu, B Spellberg, QT Phan, Y Fu, Y Fu, AS Lee, JE Edwards, SG Filler, AS Ibrahim
The Journal of clinical investigation, 2010Am Soc Clin Investig
Mucormycosis is a fungal infection of the sinuses, brain, or lungs that causes a mortality rate
of at least 50% despite first-line therapy. Because angioinvasion is a hallmark of
mucormycosis infections, we sought to define the endothelial cell receptor (s) for fungi of the
order Mucorales (the fungi that cause mucormycosis). Furthermore, since patients with
elevated available serum iron, including those with diabetic ketoacidosis (DKA), are
uniquely susceptible to mucormycosis, we sought to define the role of iron and glucose in …
Mucormycosis is a fungal infection of the sinuses, brain, or lungs that causes a mortality rate of at least 50% despite first-line therapy. Because angioinvasion is a hallmark of mucormycosis infections, we sought to define the endothelial cell receptor(s) for fungi of the order Mucorales (the fungi that cause mucormycosis). Furthermore, since patients with elevated available serum iron, including those with diabetic ketoacidosis (DKA), are uniquely susceptible to mucormycosis, we sought to define the role of iron and glucose in regulating the expression of such a receptor. Here, we have identified glucose-regulated protein 78 (GRP78) as what we believe to be a novel host receptor that mediates invasion and damage of human endothelial cells by Rhizopus oryzae, the most common etiologic species of Mucorales, but not Candida albicans or Aspergillus fumigatus. Elevated concentrations of glucose and iron, consistent with those seen during DKA, enhanced GRP78 expression and the resulting R. oryzae invasion and damage of endothelial cells in a receptor-dependent manner. Mice with DKA, which have enhanced susceptibility to mucormycosis, exhibited increased expression of GRP78 in sinus, lungs, and brain compared with normal mice. Finally, GRP78-specific immune serum protected mice with DKA from mucormycosis. These results suggest a unique susceptibility of patients with DKA to mucormycosis and provide a foundation for the development of new therapeutic interventions for these deadly infections.
The Journal of Clinical Investigation