4.7 Article

Renal dendritic cells sample blood-borne antigen and guide T-cell migration to the kidney by means of intravascular processes

Journal

KIDNEY INTERNATIONAL
Volume 90, Issue 4, Pages 818-827

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1016/j.kint.2016.05.030

Keywords

acute kidney injury; macrophages; sepsis

Funding

  1. Center for Biologic Imaging [1S10RR028478-01]
  2. American Heart Association [11SDG7230011]
  3. American Society of Nephrology Merrill Grant in Transplantation
  4. American Society of Nephrology Ben J. Lipps Research Fellowship Program, Donald E. Wesson Research Fellow

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Bony fish are among the first vertebrates to possess an innate and adaptive immune system. In these species, the kidney has a dual function: filtering solutes similar to mammals and acting as a lymphoid organ responsible for hematopoiesis and antigen processing. Recent studies have shown that the mammalian kidney has an extensive network of mononuclear phagocytes, whose function is not fully understood. Here, we employed two-photon intravital microscopy of fluorescent reporter mice to demonstrate that renal dendritic cells encase the microvasculature in the cortex, extend dendrites into the peritubular capillaries, and sample the blood for antigen. We utilized a mouse model of systemic bacterial infection as well as immune complexes to demonstrate antigen uptake by renal dendritic cells. As a consequence, renal dendritic cells mediated T-cell migration into the kidney in an antigen dependent manner in the setting of bacterial infection. Thus, renal dendritic cells may be uniquely positioned to play an important role not only in surveillance of systemic infection but also in local infection and autoimmunity.

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