Sakaguchi N, Crouch J J, Lytle C, Schulte B A
Department of Pathology and Laboratory Medicine, Medical University of South Carolina, Charleston 29425, USA.
Hear Res. 1998 Apr;118(1-2):114-22. doi: 10.1016/s0378-5955(98)00022-7.
Changes in the cellular expression pattern of the Na-K-Cl cotransporter (NKCC) were investigated during postnatal development and with advancing age in the gerbil cochlea. At birth, faint immunostaining for NKCC was discernable in the developing stria vascularis (StV), Reissner's membrane, interdental cells and some relatively undifferentiated cells lining the cochlear partition. Between 2 and 4 days after birth (DAB) immunostaining persisted and increased in the future interdental, inner and outer sulcus and claudius cells but then disappeared from these sites by 8 DAB. In contrast, NKCC immunoreactivity in the StV increased progressively during development and approached adult levels by 12 DAB. Immunostaining for NKCC in subpopulations of fibrocytes in the inferior portion of the spiral ligament, the suprastrial region and the spiral limbus was first detectable between 10 and 12 DAB and staining intensity reached adult levels around 16 DAB. Changes in NKCC expression with advancing age generally mimicked those previously observed for Na,K-ATPase in focal regions of atrophic lateral wall. Diminished immunostaining was first seen in the StV, presumably associated with the involution of the marginal cell's basolateral processes. Further atrophy culminated in complete loss of immunostaining in the StV and an associated down-regulation of NKCC expression in spiral ligament transport fibrocytes. The marked similarities in the developmental and age-related expression patterns of NKCC and Na,K-ATPase point to a high level of functional cooperativity between these two ion transport mediators, which together provide an efficient mechanism for generating and maintaining high K+ levels in endolymph and the endocochlear potential.
在沙土鼠耳蜗出生后发育期间以及随着年龄增长,研究了钠-钾-氯协同转运蛋白(NKCC)的细胞表达模式变化。出生时,在发育中的血管纹、Reissner膜、齿间细胞以及耳蜗隔板内衬的一些相对未分化的细胞中,可辨别出NKCC的微弱免疫染色。出生后2至4天(DAB),免疫染色在未来的齿间、内沟和外沟以及克劳迪乌斯细胞中持续存在并增加,但在8 DAB时从这些部位消失。相比之下,血管纹中的NKCC免疫反应性在发育过程中逐渐增加,并在12 DAB时接近成年水平。螺旋韧带下部、血管纹上区域和螺旋缘的纤维细胞亚群中NKCC的免疫染色在10至12 DAB之间首次可检测到,染色强度在16 DAB左右达到成年水平。随着年龄增长,NKCC表达的变化通常与先前在萎缩性侧壁局部区域观察到的钠钾ATP酶的变化相似。免疫染色减弱首先出现在血管纹中,可能与边缘细胞基底外侧突起的退化有关。进一步的萎缩最终导致血管纹中免疫染色完全丧失,以及螺旋韧带转运纤维细胞中NKCC表达的相关下调。NKCC和钠钾ATP酶在发育和与年龄相关的表达模式上的显著相似性表明这两种离子转运介质之间存在高度的功能协同作用,它们共同提供了一种有效的机制来产生和维持内淋巴中的高钾水平和内耳蜗电位。