Nigrovic Peter A, Gray Daniel H D, Jones Tatiana, Hallgren Jenny, Kuo Frank C, Chaletzky Blair, Gurish Michael, Mathis Diane, Benoist Christophe, Lee David M
Division of Rheumatology, Immunology and Allergy, Brigham and Women's Hospital, Boston, MA 02115, USA.
Am J Pathol. 2008 Dec;173(6):1693-701. doi: 10.2353/ajpath.2008.080407. Epub 2008 Nov 6.
Mast cells participate in pathophysiological processes that range from antimicrobial defense to anaphylaxis and inflammatory arthritis. Much of the groundwork for the understanding of mast cells was established in mice that lacked mast cells through defects in either stem cell factor or its receptor, Kit. Among available strains, C57BL/6-Kit(W-sh) (W(sh)) mice are experimentally advantageous because of their background strain and fertility. However, the genetic inversion responsible for the W(sh) phenotype remains poorly defined, and its effects beyond the mast cell have been incompletely characterized. We report that W(sh) animals exhibit splenomegaly with expanded myeloid and megakaryocyte populations. Hematopoietic abnormalities extend to the bone marrow and are reflected by neutrophilia and thrombocytosis. In contrast, mast cell-deficient WBB6F1-Kit(W)/Kit(W-v) (W/W(v)) mice display mild neutropenia, but no changes in circulating platelet numbers. To help define the basis for the W(sh) phenotype, a "DNA walking" strategy was used to identify the precise location of the 3' breakpoint, which was found to reside 67.5 kb upstream of Kit. The 5' breakpoint disrupts corin, a cardiac protease responsible for the activation of atrial natriuretic peptide. Consistent with this result, transcription of full-length corin is ablated and W(sh) mice develop symptoms of cardiomegaly. Studies performed using mast cell-deficient strains must consider the capacity of associated abnormalities to either expose or compensate for the missing mast cell lineage.
肥大细胞参与从抗菌防御到过敏反应和炎性关节炎等一系列病理生理过程。对肥大细胞的许多基础性理解是在因干细胞因子或其受体Kit缺陷而缺乏肥大细胞的小鼠中建立的。在现有品系中,C57BL/6-Kit(W-sh)(W(sh))小鼠因其背景品系和繁殖力而在实验上具有优势。然而,导致W(sh)表型的基因倒位仍定义不明确,其在肥大细胞之外的影响也未得到充分表征。我们报告W(sh)动物表现出脾脏肿大,伴有髓系细胞和巨核细胞群体扩大。造血异常延伸至骨髓,并表现为中性粒细胞增多和血小板增多。相比之下,肥大细胞缺陷的WBB6F1-Kit(W)/Kit(W-v)(W/W(v))小鼠表现出轻度中性粒细胞减少,但循环血小板数量没有变化。为了帮助确定W(sh)表型的基础,采用了“DNA步移”策略来确定3'断点的精确位置,发现其位于Kit上游67.5 kb处。5'断点破坏了corin,一种负责激活心房利钠肽的心脏蛋白酶。与这一结果一致,全长corin的转录被消除,W(sh)小鼠出现心脏肥大症状。使用肥大细胞缺陷品系进行的研究必须考虑相关异常暴露或补偿缺失肥大细胞谱系的能力。