Localization of gp130 in the developing and adult mouse cerebellum

被引:11
作者
Ha, BK [1 ]
King, JS [1 ]
机构
[1] Ohio State Univ, Dept Neurosci, Columbus, OH 43210 USA
关键词
IL-6 type cytokines; Purkinje cells; astrocytes; differentiation; neurotrophic factors;
D O I
10.1016/S0891-0618(00)00056-9
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Interleukin-6 (IL-6) type cytokines show functional redundancy in the immune, hematopoietic, and nervous system, which is believed to result from sharing of the signal transducing receptor gp130. IL-6 type cytokines and their binding receptors have been localized in the adult cerebellum. However, the cellular localization and developmental regulation of gp130 in the cerebellum have not been determined. In the present study the expression pattern of gp130 in the developing and adult mouse cerebellum was investigated. At embryonic day (E)15 and E17, gp130 immunoreactivity is present primarily in fiber bundles that course from the brainstem to the cerebellum. At postnatal day (P)0, gp130 immunoreactivity first appears in the Purkinje cell layer, external granule cell layer, and cerebellar nuclei. As Purkinje cells differentiate, gp130 immunoreactivity progressively extends from the cell body along their developing dendritic arbor. All Purkinje cells show intense gp130 immunoreactivity in their cell bodies by P7. In contrast the gp130 immunoreactivity detected in fiber bundles at E15 and E17 is downregulated postnatally, and cannot be detected after P7. Granule cells show gp130 immunoreactivity at PO in the external granule cell layer and subsequently in the internal granule cell layer. Astrocytes in the white matter express gp130 at PO, and show intense gp130 immunoreactivity between P7 and P14. As the cerebellum matures gp130 immunoreactivity in the white matter decreases. The present description of the differential spatial and temporal distribution of gp130 provides an initial step in defining specific cellular populations that are potential targets of IL-6 type cytokines during cerebellar ontogeny. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:129 / 141
页数:13
相关论文
共 69 条
[1]  
ASHWELL KWS, 1992, ACTA ANAT, V145, P17
[2]   EVIDENCE THAT MOUSE ASTROCYTES MAY BE DERIVED FROM THE RADIAL GLIA - AN IMMUNOHISTOCHEMICAL STUDY OF THE CEREBELLUM IN THE NORMAL AND REELER MOUSE [J].
BENJELLOUNTOUIMI, S ;
JACQUE, CM ;
DERER, P ;
DEVITRY, F ;
MAUNOURY, R ;
DUPOUEY, P .
JOURNAL OF NEUROIMMUNOLOGY, 1985, 9 (1-2) :87-97
[3]   Postnatally induced inactivation of gp130 in mice results in neurological, cardiac, hematopoietic, immunological, hepatic, and pulmonary defects [J].
Betz, UAK ;
Bloch, W ;
van den Broek, M ;
Yoshida, K ;
Taga, T ;
Kishimoto, T ;
Addicks, K ;
Rajewsky, K ;
Müller, W .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 188 (10) :1955-1965
[4]   LOCALIZATION OF VIMENTIN, THE NONSPECIFIC INTERMEDIATE FILAMENT PROTEIN, IN EMBRYONAL GLIA AND IN EARLY DIFFERENTIATING NEURONS - INVIVO AND INVITRO IMMUNOFLUORESCENCE STUDY OF THE RAT EMBRYO WITH VIMENTIN AND NEUROFILAMENT ANTISERA [J].
BIGNAMI, A ;
RAJU, T ;
DAHL, D .
DEVELOPMENTAL BIOLOGY, 1982, 91 (02) :286-295
[5]  
Blesch A, 1999, J NEUROSCI, V19, P3556
[6]   Regulation of gliogenesis in the central nervous system by the JAK-STAT signaling pathway [J].
Bonni, A ;
Sun, Y ;
NadalVicens, M ;
Bhatt, A ;
Frank, DA ;
Rozovsky, I ;
Stahl, N ;
Yancopoulos, GD ;
Greenberg, ME .
SCIENCE, 1997, 278 (5337) :477-483
[7]  
BOVOLENTA P, 1984, DEV BIOL, V102, P248, DOI 10.1016/0012-1606(84)90189-1
[8]  
Cui Q, 1999, INVEST OPHTH VIS SCI, V40, P760
[9]   LIFR-BETA AND GP-130 AS HETERODIMERIZING SIGNAL TRANSDUCERS OF THE TRIPARTITE CNTF RECEPTOR [J].
DAVIS, S ;
ALDRICH, TH ;
STAHL, N ;
PAN, L ;
TAGA, T ;
KISHIMOTO, T ;
IP, NY ;
YANCOPOULOS, GD .
SCIENCE, 1993, 260 (5115) :1805-1808
[10]   gp130-mediated signal transduction in embryonic stem cells involves activation of Jak and Ras/mitogen-activated protein kinase pathways [J].
Ernst, M ;
Oates, A ;
Dunn, AR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (47) :30136-30143