Depletion of collagen IX alpha1 impairs myeloid cell function

Publikation: Forschung - BegutachtungZeitschriftenaufsätze

AutorInnen

  • Kristina Probst
  • Jacek Stermann
  • Inga von Bomhard
  • Julia Etich
  • Lena Pitzler
  • Anja Niehoff
  • Björn Bluhm
  • Haifeng C Xu
  • Philipp A Lang
  • Markus Chmielewski
  • Hinrich Abken
  • Birgit Blissenbach
  • Alzbeta Machova
  • Nikoletta Papadopoulou
  • Bent Brachvogel

Forschungseinrichtungen

Details

The trabecular extracellular matrix (ECM) forms a three-dimensional scaffold to stabilize the bone marrow, provide substrates for cell-matrix interactions and retain, present or release signals to modulate hematopoietic stem and progenitor cell development. However, the impact of trabecular ECM components on hematopoiesis has been poorly studied. Using collagen IX alpha1 - deficient (Col9a1[-/-] ) mice, we revealed that a lack of collagen IX alpha1 results in a disorganized trabecular network enriched in fibronectin, and in a reduction in myeloid cells, which was accompanied by a decrease in CSF1R expression on monocytes from the bone marrow. In contrast, B-cell numbers in the bone marrow and T-cell numbers in the thymus remained unchanged. Alterations in the bone marrow microenvironment may not only reduce myeloid cell numbers, but also have long-term implications for myeloid cell function. Mice were infected with Listeria moncytogenes to analyze the function of myeloid cells. In this case, an inadequate macrophage-dependent clearance of bacterial infections was observed in Col9a1[-/-] mice in vivo. This was mainly caused by an impaired interferon-gamma / tumor necrosis factor-alpha-mediated activation of macrophages. The loss of collagen IX alpha1 therefore destabilizes the trabecular bone network, impairs myeloid cell differentiation and affects the innate immune response against Listeria. © AlphaMed Press 2018.

OriginalspracheEnglisch
ZeitschriftStem cells (Dayton, Ohio)
ISSN1066-5099
DOIs
ZustandVeröffentlicht - 31.07.2018

ID: 3449349

DOI

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