Inadequate cytoplasmatic calcium signals in alveolar macrophages after cardiac surgery

Katharina Berger1, Michael Sander, Anke Kohlar

  • 1Department of Anesthesiology and Intensive Care Medicine, Charité-Universitätsmedizin Berlin, Berlin, Germany.

Abstract

Insights

Cardiac surgery impairs alveolar macrophage function by reducing intracellular calcium signaling, potentially increasing postoperative lung infection risk. This study assessed calcium signals in macrophages before and after surgery.

Area of Science:

  • Immunology
  • Cellular Biology
  • Cardiothoracic Surgery

Background:

  • Patients undergoing cardiac surgery face heightened risks of pulmonary complications.
  • Alveolar macrophage (AM) dysfunction may contribute to postoperative infections.
  • Intracellular calcium ([Ca(2+)](i)) is a critical second messenger in cellular signaling.

Purpose of the Study:

  • To assess intracellular calcium ([Ca(2+)](i)) signaling in alveolar macrophages (AMs) from patients before and after cardiac surgery.
  • To investigate the potential link between AM dysfunction and postoperative pulmonary complications.

Main Methods:

  • Clinical trial involving 12 patients undergoing coronary artery bypass graft (CABG) surgery.
  • Bronchoalveolar lavage (BAL) fluid collected preoperatively and postoperatively.
  • Flow cytometry used to assess AM subpopulations and [Ca(2+)](i) signals via the Fluo4/FuraRed-Ratio.

Main Results:

  • A significant reduction in baseline [Ca(2+)](i) in unstimulated AMs was observed post-surgery (p < 0.001).
  • AMs showed significantly reduced signal responses to fMLP (p = 0.021) and C5a (p = 0.028) stimulation after surgery.
  • A trend towards reduced responsiveness was noted across all AM populations post-surgery.

Conclusions:

  • Reduced [Ca(2+)](i) signaling in postoperative AMs may stem from impaired coupling to membrane channels.
  • Preliminary findings suggest inadequate AM [Ca(2+)](i) signaling post-surgery, potentially leading to local immune dysfunction in the lungs.

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