Department of Chemical and Biomolecular Engineering, University of Illinois at Urbana-Champaign, Urbana, Illinois, United States of America.
Department of Pathology, University of Michigan, Ann Arbor, Michigan, United States of America.
PLoS One. 2014 Jan 21;9(1):e85726. doi: 10.1371/journal.pone.0085726. eCollection 2014.
Neutrophils constitute the largest class of white blood cells and are the first responders in the innate immune response. They are able to sense and migrate up concentration gradients of chemoattractants in search of primary sites of infection and inflammation through a process known as chemotaxis. These chemoattractants include formylated peptides and various chemokines. While much is known about chemotaxis to individual chemoattractants, far less is known about chemotaxis towards many. Previous studies have shown that in opposing gradients of intermediate chemoattractants (interleukin-8 and leukotriene B4), neutrophils preferentially migrate toward the more distant source. In this work, we investigated neutrophil chemotaxis in opposing gradients of chemoattractants using a microfluidic platform. We found that primary neutrophils exhibit oscillatory motion in opposing gradients of intermediate chemoattractants. To understand this behavior, we constructed a mathematical model of neutrophil chemotaxis. Our results suggest that sensory adaptation alone cannot explain the observed oscillatory motion. Rather, our model suggests that neutrophils employ a winner-take-all mechanism that enables them to transiently lock onto sensed targets and continuously switch between the intermediate attractant sources as they are encountered. These findings uncover a previously unseen behavior of neutrophils in opposing gradients of chemoattractants that will further aid in our understanding of neutrophil chemotaxis and the innate immune response. In addition, we propose a winner-take-all mechanism allows the cells to avoid stagnation near local chemical maxima when migrating through a network of chemoattractant sources.
中性粒细胞构成了白细胞的最大群体,是先天免疫反应的第一响应者。它们能够感知并沿着趋化因子浓度梯度迁移,以寻找感染和炎症的主要部位,这个过程被称为趋化作用。这些趋化因子包括甲酰肽和各种趋化因子。虽然人们对单个趋化因子的趋化作用了解很多,但对许多趋化因子的趋化作用了解甚少。以前的研究表明,在中间趋化因子(白细胞介素-8 和白三烯 B4)的相反梯度中,中性粒细胞优先向更远的来源迁移。在这项工作中,我们使用微流控平台研究了中性粒细胞在相反趋化因子梯度中的趋化作用。我们发现原发性中性粒细胞在中间趋化因子的相反梯度中表现出振荡运动。为了理解这种行为,我们构建了一个中性粒细胞趋化性的数学模型。我们的结果表明,仅感官适应不能解释观察到的振荡运动。相反,我们的模型表明,中性粒细胞采用一种胜者全取机制,使它们能够暂时锁定感知到的目标,并在遇到中间吸引源时不断在它们之间切换。这些发现揭示了中性粒细胞在相反趋化因子梯度中以前未被发现的行为,这将进一步帮助我们理解中性粒细胞趋化性和先天免疫反应。此外,我们提出的胜者全取机制允许细胞在通过趋化因子源网络迁移时避免在局部化学最大值附近停滞。