腸道巨噬細(xì)胞代表了多種的常駐組織巨噬細(xì)胞來源 [1, 2]。腸道常駐巨噬細(xì)胞是一種重要的免疫群體，能夠在其環(huán)境中整合和解釋不同的食物來源、共生來源、病原體來源和宿主來源的信號(hào)。此外，在炎癥反應(yīng)下，BM 衍生的腸道巨噬細(xì)胞和常駐巨噬細(xì)胞在控制感染中起關(guān)鍵作用。因此，腸道巨噬細(xì)胞池的動(dòng)態(tài)調(diào)節(jié)是長(zhǎng)期健康的核心[3]。補(bǔ)充健康腸道中常駐池的 BM 衍生巨噬細(xì)胞被確定為 CX3CR1hiMHCIIhiLy6Clow [103]，它們?cè)谀c道穩(wěn)態(tài)中具有多種關(guān)鍵功能，包括 Treg 擴(kuò)增、上皮維持、管腔取樣和細(xì)菌殺滅 [4, 5]。如表 4 所示，腸道和真皮被認(rèn)為是開放組織，具有快速募集和分化骨髓來源的單核細(xì)胞成巨噬細(xì)胞的動(dòng)力學(xué)。盡管在出生時(shí)，腸道中存在胚胎衍生的巨噬細(xì)胞，但這些巨噬細(xì)胞被來自大量 CCR2 依賴性 Ly6Chi 單核細(xì)胞的細(xì)胞所取代[6]。巨噬細(xì)胞上的 IL-10 受體信號(hào)傳導(dǎo)是一種對(duì)指導(dǎo)胃腸粘膜中巨噬細(xì)胞功能至關(guān)重要的途徑 [7, 8]。
如何研究腸道巨噬細(xì)胞的功能？一個(gè)強(qiáng)有力的工具就是清除腸道巨噬細(xì)胞。靶點(diǎn)科技庫(kù)存大量LIPOSOMA的ClodronateLiposomes氯膦酸二鈉脂質(zhì)體。作為授權(quán)的中國(guó)Exclusive Distributor，無論從產(chǎn)品質(zhì)量還是技術(shù)支持，都能給予從理論到實(shí)踐的賦能。
參考文獻(xiàn)
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2. Lee S, Starkey P, Gordon S. Quantitative analysis of total macrophage content in adult mouse tissues. Immunochemical studies with monoclonal antibody F4/80. J Exp Med. 1985;161:475-89
3. Grainger J, Konkel J, Zangerle Murray T, Shaw T. Macrophages in gastrointestinal homeostasis and inflammation. Pflugers Arch. 2017;469:527-539
4. Bain C, Scott C, Uronen Hansson H, Gudjonsson S, Jansson O, Grip O, et al. Resident and pro-inflammatory macrophages in the colon represent alternative context-dependent fates of the same Ly6Chi monocyte precursors. Mucosal Immunol. 2013;6:498-510
5. Hadis U, Wahl B, Schulz O, Hardtke Wolenski M, Schippers A, Wagner N, et al. Intestinal tolerance requires gut homing and expansion of FoxP3+ regulatory T cells in the lamina propria. Immunity. 2011;34:237-46
6. Smythies L, Sellers M, Clements R, Mosteller Barnum M, Meng G, Benjamin W, et al. Human intestinal macrophages display profound inflammatory anergy despite avid phagocytic and bacteriocidal activity. J Clin Invest. 2005;115:66-75
7. Bain C, Bravo Blas A, Scott C, Perdiguero E, Geissmann F, Henri S, et al. Constant replenishment from circulating monocytes maintains the macrophage pool in the intestine of adult mice. Nat Immunol. 2014;15:929-937
8. Shouval D, Biswas A, Goettel J, McCann K, Conaway E, Redhu N, et al. Interleukin-10 receptor signaling in innate immune cells regulates mucosal immune tolerance and anti-inflammatory macrophage function. Immunity. 2014;40:706-19
9. Zigmond E, Bernshtein B, Friedlander G, Walker C, Yona S, Kim K, et al. Macrophage-restricted interleukin-10 receptor deficiency, but not IL-10 deficiency, causes severe spontaneous colitis. Immunity. 2014;40:720-33
