{"title":"从全血中分离低密度和正常密度中性粒细胞并确定其特征。","authors":"Anjali S Yennemadi, Joseph Keane, Gina Leisching","doi":"10.3791/67805","DOIUrl":null,"url":null,"abstract":"<p><p>Emerging research shows that the circulating neutrophil population in humans consists of diverse subtypes and should not be studied as a single population, as has been done historically. In particular, low-density and normal-density neutrophils (LDNs, NDNs) have been shown to have functionally and metabolically distinct profiles, a factor that must be considered when publishing neutrophil research. Here, we present a modified method for the untouched isolation and separation of LDNs and NDNs from whole blood. The density gradient medium (1.135 g/mL) is combined at 9:10 with 10x PBS. Specific density gradients of 55%, 70%, and 81% are subsequently made by combining the 100% density gradient medium with 1x phosphate-buffered saline (PBS). Neutrophils isolated from 12 mL of peripheral whole blood obtained from consented donors using a negative selection-based magnetic isolation kit are resuspended in the 55% fraction. A volume of 3 mL of the 81% and 70% fractions is layered into a 15 mL tube, followed by the 55% fraction containing total neutrophils. The density gradients are then centrifuged at 720 x g for 30 min. Two distinct bands are obtained at the 55%/70% interface (LDNs) and 70%/81% interface (NDNs). The cells are carefully pipetted into separate tubes and washed using PBS. The purity of the isolated fractions is determined using flow cytometry. Both LDNs and NDNs were defined as CD14lo CD15+ SSChi by flow cytometry. Isolation purity was calculated at ≥93% of viable cells for both types. This method provides a reliable and efficient approach for separating LDN and NDNs from peripheral blood, ensuring high purity and viability of the isolated cells. Enhancing the precision of neutrophil isolation facilitates more accurate downstream analyses of these distinct neutrophil subpopulations. These are critical for advancing our understanding of neutrophil heterogeneity and its implications in various physiological and pathological contexts.</p>","PeriodicalId":48787,"journal":{"name":"Jove-Journal of Visualized Experiments","volume":" 216","pages":""},"PeriodicalIF":1.2000,"publicationDate":"2025-02-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"The Isolation and Characterization of Low- and Normal- Density Neutrophils from Whole Blood.\",\"authors\":\"Anjali S Yennemadi, Joseph Keane, Gina Leisching\",\"doi\":\"10.3791/67805\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Emerging research shows that the circulating neutrophil population in humans consists of diverse subtypes and should not be studied as a single population, as has been done historically. In particular, low-density and normal-density neutrophils (LDNs, NDNs) have been shown to have functionally and metabolically distinct profiles, a factor that must be considered when publishing neutrophil research. Here, we present a modified method for the untouched isolation and separation of LDNs and NDNs from whole blood. The density gradient medium (1.135 g/mL) is combined at 9:10 with 10x PBS. Specific density gradients of 55%, 70%, and 81% are subsequently made by combining the 100% density gradient medium with 1x phosphate-buffered saline (PBS). Neutrophils isolated from 12 mL of peripheral whole blood obtained from consented donors using a negative selection-based magnetic isolation kit are resuspended in the 55% fraction. A volume of 3 mL of the 81% and 70% fractions is layered into a 15 mL tube, followed by the 55% fraction containing total neutrophils. The density gradients are then centrifuged at 720 x g for 30 min. Two distinct bands are obtained at the 55%/70% interface (LDNs) and 70%/81% interface (NDNs). The cells are carefully pipetted into separate tubes and washed using PBS. The purity of the isolated fractions is determined using flow cytometry. Both LDNs and NDNs were defined as CD14lo CD15+ SSChi by flow cytometry. Isolation purity was calculated at ≥93% of viable cells for both types. This method provides a reliable and efficient approach for separating LDN and NDNs from peripheral blood, ensuring high purity and viability of the isolated cells. Enhancing the precision of neutrophil isolation facilitates more accurate downstream analyses of these distinct neutrophil subpopulations. 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引用次数: 0
摘要
新出现的研究表明,人类循环中性粒细胞群体由不同的亚型组成,不应像以往那样作为单一群体进行研究。特别是,低密度和正常密度中性粒细胞(ldn, ndn)已被证明具有不同的功能和代谢特征,这是发表中性粒细胞研究时必须考虑的一个因素。在这里,我们提出了一种改进的方法,用于从全血中分离和分离ldn和ndn。密度梯度培养基(1.135 g/mL)以9:10与10倍PBS混合。随后,通过将100%密度梯度培养基与1x磷酸盐缓冲盐水(PBS)混合,制成55%、70%和81%的比密度梯度。使用阴性选择磁分离试剂盒从同意的献血者获得的12ml外周全血中分离出中性粒细胞,在55%的分数中重悬。将体积为3ml的81%和70%的分数分层放入15ml的管中,然后放入含有总中性粒细胞的55%的分数。然后将密度梯度在720 x g下离心30分钟。在55%/70%界面(LDNs)和70%/81%界面(NDNs)处获得两个不同的条带。将细胞小心地移液到不同的管中,并用PBS洗涤。用流式细胞术测定分离馏分的纯度。流式细胞术将ldn和ndn定义为CD14lo CD15+ SSChi。两种细胞的分离纯度均为≥93%。该方法为从外周血中分离LDN和ndn提供了一种可靠、高效的方法,保证了分离细胞的高纯度和活力。提高中性粒细胞分离的精度有助于对这些不同的中性粒细胞亚群进行更准确的下游分析。这些对于我们理解中性粒细胞的异质性及其在各种生理和病理背景下的影响至关重要。
The Isolation and Characterization of Low- and Normal- Density Neutrophils from Whole Blood.
Emerging research shows that the circulating neutrophil population in humans consists of diverse subtypes and should not be studied as a single population, as has been done historically. In particular, low-density and normal-density neutrophils (LDNs, NDNs) have been shown to have functionally and metabolically distinct profiles, a factor that must be considered when publishing neutrophil research. Here, we present a modified method for the untouched isolation and separation of LDNs and NDNs from whole blood. The density gradient medium (1.135 g/mL) is combined at 9:10 with 10x PBS. Specific density gradients of 55%, 70%, and 81% are subsequently made by combining the 100% density gradient medium with 1x phosphate-buffered saline (PBS). Neutrophils isolated from 12 mL of peripheral whole blood obtained from consented donors using a negative selection-based magnetic isolation kit are resuspended in the 55% fraction. A volume of 3 mL of the 81% and 70% fractions is layered into a 15 mL tube, followed by the 55% fraction containing total neutrophils. The density gradients are then centrifuged at 720 x g for 30 min. Two distinct bands are obtained at the 55%/70% interface (LDNs) and 70%/81% interface (NDNs). The cells are carefully pipetted into separate tubes and washed using PBS. The purity of the isolated fractions is determined using flow cytometry. Both LDNs and NDNs were defined as CD14lo CD15+ SSChi by flow cytometry. Isolation purity was calculated at ≥93% of viable cells for both types. This method provides a reliable and efficient approach for separating LDN and NDNs from peripheral blood, ensuring high purity and viability of the isolated cells. Enhancing the precision of neutrophil isolation facilitates more accurate downstream analyses of these distinct neutrophil subpopulations. These are critical for advancing our understanding of neutrophil heterogeneity and its implications in various physiological and pathological contexts.
期刊介绍:
JoVE, the Journal of Visualized Experiments, is the world''s first peer reviewed scientific video journal. Established in 2006, JoVE is devoted to publishing scientific research in a visual format to help researchers overcome two of the biggest challenges facing the scientific research community today; poor reproducibility and the time and labor intensive nature of learning new experimental techniques.