Sahi J, Nataraja S G, Layden T J, Goldstein J L, Moyer M P, Rao M C
Department of Physiology and Biophysics, University of Illinois at Chicago, Chicago, Illinois 60612, USA.
Am J Physiol. 1998 Oct;275(4):C1048-57. doi: 10.1152/ajpcell.1998.275.4.C1048.
Cells of a newly described, immortalized, epithelial, human transverse colonic cell line, NCM460, reach approximately 90% confluence on plastic and develop transepithelial resistances of 120-250 Omega . cm2 on porous substrates. Its utility as a model for the transverse human colon was validated by comparing second messenger-mediated Cl- transport, using the fluorescent probe 6-methoxy-quinolyl acetoethyl ester, in NCM460 cells and colonocytes isolated from human transverse crypts. Basal Cl- influx was increased (P < 0.01) by PGE1 (1 microM), forskolin (1 microM), 8-bromoadenosine 3'5'-cyclic monophosphate (100 microM), heat-stable Escherichia coli enterotoxin (STa; 1 microM), 8-bromoguanosine 3'5'-cyclic monophosphate (100 microM), histamine (1 microM), and phorbol 12,13-dibutyrate (1 microM) in both cell types. The Cl- channel blocker diphenylamine 2-carboxylic acid (50 microM) and the Na+-K+-2Cl- cotransport inhibitor furosemide (1 microM), but not the K+ channel blocker Ba2+ (3 mM), inhibited these Cl- permeabilities. These cells possess transcripts for cystic fibrosis transmembrane conductance regulator, Na+-K+-2Cl- cotransporter, STa receptor, and intestine-specific cGMP-dependent protein kinase II. Thus cAMP-, cGMP-, and Ca2+-dependent secretagogues act on NCM460 and primary colonocytes to stimulate Cl- transport. This validates the utility of NCM460 as a model for transverse colonic crypts and is the first demonstration of a colonic cell line whose origin is known.
一种新描述的永生化人横结肠上皮细胞系NCM460,其细胞在塑料培养皿上达到约90%汇合度,并在多孔基质上形成120 - 250Ω.cm²的跨上皮电阻。通过比较使用荧光探针6 - 甲氧基喹啉基乙酰乙酯在NCM460细胞和从人横结肠隐窝分离的结肠细胞中第二信使介导的Cl⁻转运,验证了其作为人横结肠模型的实用性。在两种细胞类型中,PGE1(1μM)、福斯可林(1μM)、8 - 溴腺苷3',5'-环磷酸(100μM)、热稳定大肠杆菌肠毒素(STa;1μM)、8 - 溴鸟苷3',5'-环磷酸(100μM)、组胺(1μM)和佛波醇12,13 - 二丁酸酯(1μM)均可增加基础Cl⁻内流(P < 0.01)。Cl⁻通道阻滞剂二苯胺2 - 羧酸(50μM)和Na⁺-K⁺-2Cl⁻协同转运抑制剂呋塞米(1μM)可抑制这些Cl⁻通透性,但K⁺通道阻滞剂Ba²⁺(3mM)则无此作用。这些细胞具有囊性纤维化跨膜传导调节因子、Na⁺-K⁺-2Cl⁻协同转运体、STa受体和肠特异性cGMP依赖性蛋白激酶II的转录本。因此,cAMP、cGMP和Ca²⁺依赖性促分泌剂作用于NCM460和原代结肠细胞以刺激Cl⁻转运。这验证了NCM460作为横结肠隐窝模型的实用性,并且首次证明了一种起源已知的结肠细胞系。