Posted on 22 July 2020
The study, led by scientists at the University of York, reveals how B-cells – crucial agents of the immune response – are faced with a perilous path, swimming through a dense network of other cells, blood and lymphatic vessels, to reach the follicles of the lymph nodes.
Important step forward
The research team discovered that structures inside lymph nodes leave a trail of chemical signals that guide B-cells through these complex tissues – like miniature lighthouses guiding a safe shipping passage.
Once they have reached the lymph nodes (glands which function as filters trapping viruses and bacteria before they can infect other parts of the body) B-cells confront invading pathogens and take molecules from their surfaces known as antigens. They process and present these to T cells, which then manufacture antibodies allowing them to identify and destroy the invaders.
The research is an important step forward in understanding how our immune system works and also why it fails, the authors of the study say.
Co-lead author of the study, Professor Mark Leake, from the Physics of Life group in the Department of Physics at the University of York, said: “Our study suggests that B-cells sniff out a chemical trail which allows them to swim over relatively long distances in a highly complex microenvironment to reach their key destination.
“Relying on a single chemical transmitter to act as a beacon across the whole of the lymph node wouldn’t do the trick, since the signal becomes too dilute and swamped by noise. Instead, these multiple signals are like having a trail of breadcrumbs that the cells can follow.”
The study may solve the mystery of how cells which are a hundred times smaller than a millimetre are able to travel over distances of around a metre to get to where they are needed in the body.
An international team of researchers from multiple disciplines including immunology, biophysics, cell biology, mathematics and computer science contributed to the research.
The team used fluorescent tags on signalling molecules to track their location in the lymph nodes of mice and human biopsy samples. They employed maths modelling and computer simulations involving machine learning to map out the cell architecture of the follicles of lymph node tissues.
Prof Leake added: “The only way we could gain this incredible new insight is by forming a large research team with a broad range of expertise crossing between multiple traditional science disciplines.
“Research into understanding the workings of the immune system at the scale of single molecules may help us to understand why things go wrong in the case of some diseases of the immune system. It may help pave the way to new drugs that help to improve the immune system’s ability to combat emerging threats from harmful viruses and bacteria that the human population have not previously encountered.”
B cell Zone Reticular Cell Microenvironments Shape CXCL13 Gradient Formation is published in the journal Nature Communications. The study was funded by the Medical Research Council, the Biology and Biotechnology Research Council, the Engineering and Physical Sciences Research Council, the Swiss National Science Foundation, the Wellcome Trust, and the Human Frontier Science Programme.
The study involved an international research team from the Universities of York and Oxford (UK), Bern, St. Galen, Bellinzona, Fribourg and Konstanz (Switzerland), the Erasmus University Medical Centre (Netherlands), and the Université Paris Descartes (France).
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