Prin-Mathieu C, Le Roux Y, Faure G C, Laurent F, Béné M C, Moussaoui F
Laboratoire d'Immunologie, Groupe de Recherche en ImmunoPathologie, Faculté de Médecine de Nancy. Laboratoire des Sciences Animales, ENSAIA, 54500 Vandoeuvre les Nancy, France.
Clin Diagn Lab Immunol. 2002 Jul;9(4):812-7. doi: 10.1128/cdli.9.4.812-817.2002.
Leukocytes are recruited from peripheral blood into milk as part of the inflammatory response to mastitis. However, excessive accumulation of inflammatory cells alters the quality of milk and the proteases produced by polymorphonuclear neutrophils (PMNs) and macrophages may lead to mammary tissue damage. To investigate PMN recruitment and the kinetics of their intracytoplasmic enzymes in inflammation, we generated mastitis in six cows by intramammary infusion of lipopolysaccharide (LPS). Clinical signs of acute mastitis were observed in all of the cows, and normal status was resumed by 316 h. Intracytoplasmic elastase, collagenase, and cathepsin activities were measured within live cells by flow cytometry in peripheral blood leukocytes and milk PMNs before and during the inflammatory process (at 10 time points between 4 and 316 h). The proportion of immature PMNs was appreciated by CD33 surface labeling measured in flow cytometry. Leukopenia was observed in the peripheral blood 4 h postinfusion, concomitant to an increase in somatic cell counts in milk. CD33(+) PMNs were preferentially recruited from the peripheral blood to milk. Enzymatic activities were detected in PMNs, lymphocytes, and monocytes at levels depending on the cell type, sample nature, and time of collection. Milk PMNs had lower enzymatic activities than peripheral blood PMNs. This study showed that milk PMNs recruited during LPS-induced experimental mastitis have an immature phenotype and significantly lower enzymatic activities than peripheral blood PMNs. This suggests that CD33, an adhesion molecule, may be involved in the egress from blood to milk and that the enzymatic contents of PMNs are partly used during this process.
作为乳腺炎炎症反应的一部分,白细胞从外周血募集到乳汁中。然而,炎症细胞的过度积累会改变乳汁质量,多形核中性粒细胞(PMN)和巨噬细胞产生的蛋白酶可能导致乳腺组织损伤。为了研究炎症过程中PMN的募集及其胞浆内酶的动力学,我们通过向六头奶牛的乳腺内注射脂多糖(LPS)来诱发乳腺炎。所有奶牛均出现急性乳腺炎的临床症状,并在316小时后恢复正常状态。在炎症过程之前和期间(在4至316小时之间的10个时间点),通过流式细胞术测量外周血白细胞和乳汁PMN中活细胞内的弹性蛋白酶、胶原酶和组织蛋白酶活性。通过流式细胞术测量CD33表面标记来评估未成熟PMN的比例。注射后4小时在外周血中观察到白细胞减少,同时乳汁中的体细胞计数增加。CD33(+) PMN优先从外周血募集到乳汁中。在PMN、淋巴细胞和单核细胞中检测到的酶活性水平取决于细胞类型、样本性质和采集时间。乳汁PMN的酶活性低于外周血PMN。本研究表明,在LPS诱导的实验性乳腺炎期间募集的乳汁PMN具有未成熟的表型,其酶活性明显低于外周血PMN。这表明粘附分子CD33可能参与了从血液到乳汁的迁移过程,并且在此过程中PMN的酶成分被部分利用。