CC and CXC chemokines Y-27632 datasheet seem the most relevant subfamilies in cerebral ischemia, since they recruit neutrophils and monocytes, which present an important phagocytic activity [4]. A wide number of studies focused on the analysis of chemokines evidence their relevant role in cerebral ischemia and show an increased expression of these molecules within the ischemic brain regions. However, non-concluding remarks can be obtained regarding its plausible role as biomarkers in the diagnosis or prognosis of stroke (Table 1). The response to inflammation within the brain involves all the cellular components of the neurovascular unit as both, producers of and responders to inflammatory molecules.

As examples, endothelial cells express cell adhesion molecules that facilitate leukocytes infiltration in response to chemokines; glial cells can secrete chemokines after ischemic stimulus; and neurons suffer the deleterious selleck chemicals llc effects of inflammation in the injured tissue (reviewed in [5]). On the other hand, chemokines are also involved in other biological functions affecting neurovascular unit components, such as angiogenesis or neuronal survival [6]. Considering all these precedents, we aimed to study the expression of chemokines by several

components of the neurovascular unit after stroke. For that purpose, we have combined two precise techniques: a multiple ELISA array of nine chemokines from CC and CXC families and laser microdissection to obtain neurons and blood brain vessels from

patients who died following an ischemic stroke. Moreover, in order to assess the plausible use of chemokines as biomarkers or therapeutic targets in stroke field, we evaluated their temporal profile in blood samples and their association with stroke severity and outcome. Four deceased patients who had an ischemic stroke secondary to Protein tyrosine phosphatase middle cerebral artery (MCA) occlusion within the previous 4 days (range, 40–100 h) were included in this part of the study (Supplementary Table 1). Brain tissue sampling from infarcted core and healthy contralateral areas was performed within the first hours after death according to our previously published procedure [7]. All samples were snap frozen in liquid nitrogen and immediately stored at −80 °C until use. Differential diagnosis of stroke was based on clinical examination by an expert neurologist and supported by computed tomography. In all cases, stroke onset was defined as the last time the patient was known to be asymptomatic. Description of demographic and clinical factors of patients that were included in this study is shown in Supplementary Table 2. Patients from the placebo arm of the MISTICS study [8] were considered for exploring blood temporal profile. From that cohort, 20 patients with a cortical ischemic stroke admitted to the emergency department within the first 3–12 h after symptoms onset were included in the study.