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在炎症的嘈杂环境中筛选信号。

Sorting the signals from the signals in the noisy environment of inflammation.

机构信息

Department of Pathology, Ward Building 3-140, Northwestern University Feinberg School of Medicine, 303 East Chicago Avenue, Chicago, IL 60611, USA.

出版信息

Sci Signal. 2011 Apr 26;4(170):pe23. doi: 10.1126/scisignal.2002051.

Abstract

Necrotic cells release dozens, possibly hundreds, of molecules that stimulate the inflammatory response. Healthy cells in the environment react to these by secreting other inflammatory mediators to amplify the response. In response to acute necrotic injury in the liver, neutrophils follow a restricted set of molecular cues to move along the sinusoids through the inflamed tissue and into the zone of necrosis, as demonstrated by intravital microscopy to view leukocyte migration live and in real time. Necrosis initiates an intricate interplay between damage-associated molecular pattern molecules, stromal inflammatory cells, and neutrophils. This results in a series of clear molecular signals, enabling neutrophils to follow an intravascular chemokine gradient along the sinusoid in the region where blood still circulates and a formyl peptide gradient through the nonperfused region to the necrotic focus.

摘要

坏死细胞释放数十种,甚至数百种分子,刺激炎症反应。环境中的健康细胞通过分泌其他炎症介质来对此做出反应,以放大反应。在活体显微镜下观察到,在肝脏的急性坏死性损伤中,中性粒细胞沿着窦状隙沿着炎症组织移动到坏死区,遵循一套严格的分子线索,以实时观察白细胞的迁移。坏死引发了损伤相关分子模式分子、基质炎症细胞和中性粒细胞之间的复杂相互作用。这导致了一系列明确的分子信号,使中性粒细胞能够沿着仍在循环的血液区域的窦状隙中的血管趋化因子梯度和穿过非灌注区域到坏死灶的甲酰肽梯度移动。

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