Developmental restriction of the LIM homeodomain transcription factor Islet-1 expression to cholinergic neurons in the rat striatum

被引:75
作者
Wang, HF
Liu, FC [1 ]
机构
[1] Natl Yang Ming Univ, Inst Neurosci, Taipei 112, Taiwan
[2] Natl Yang Ming Univ, Dept Life Sci, Taipei 112, Taiwan
关键词
basal ganglia; ganglionic eminence; differentiation; ChAT; trk A; DARPP-32;
D O I
10.1016/S0306-4522(00)00590-X
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
LIM homeodomain transcription factors play crucial roles in determining diverse aspects of neuronal development both in vertebrates and invertebrates. In the present study, we studied the expression pattern of Islet-1 (Isl-1), a member of the LIM homeodomain protein family, in the rat striatum during development. The developmental expression of Isl-1 in the striatum is highly dynamic and complex in terms of spatial and temporal regulation. The reverse transcription-polymerase chain reaction and ribonuclease protection assays demonstrated that Isl-1 messenger RNA was expressed in the developing striatum. The immunocytochemical study of Isl-1 protein expression showed that there were prominent mediolateral and caudorostral Isl-1 gradients in the developing striatum. Numerous Isl-1-positive cells appeared in the medial mantle zone of the developing striatal proper, and they co-expressed the postmitotic neuronal marker, microtubule-associated protein 2. The numbers of Isl-1-positive cells were decreased from the medial to the lateral regions, so that there were only a few Isl-1-positive cells scattered in the lateral striatum. These scattered Isl-1-positive cells were doubly labeled with tyrosine kinase receptor A and choline acetyltransferase, which indicated that they were cholinergic neurons. The Isl-1 gradients were most prominent in the embryonic day 18 and 20 striatum. With increases of time, the Isl-1 gradients were gradually reduced, and the gradients disappeared by postnatal day 7. Despite the general down-regulation of striatal Isl-1, a few Isl-1-positive cells were sustained into the adult striatum in which Isl-1 was nearly exclusively expressed by all cholinergic neurons and vice versa. Our study suggests that Isl-1 is likely to be initially expressed by postmitotic cholinergic precursors and some, if not all, non-cholinergic precursors in the developing striatum. During the progression of striatal differentiation, Isl-1 is downregulated in non-cholinergic cells, but is sustained in cholinergic cells. The developmental restriction of Isl-1 to cholinergic neurons in the striatum may represent a novel mechanism by which LIM homeodomain proteins specify specific cell types in the striatum during development. (C) 2001 IBRO. Published by Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:999 / 1016
页数:18
相关论文
共 72 条
[21]   Cell birth, cell death, cell diversity and DNA breaks: how do they all fit together? [J].
Gilmore, EC ;
Nowakowski, RS ;
Caviness, VS ;
Herrup, K .
TRENDS IN NEUROSCIENCES, 2000, 23 (03) :100-105
[22]  
Graybiel A. M., 1999, HDB CHEM NEUROANAT 3, P227
[23]   NEUROTRANSMITTERS AND NEUROMODULATORS IN THE BASAL GANGLIA [J].
GRAYBIEL, AM .
TRENDS IN NEUROSCIENCES, 1990, 13 (07) :244-254
[24]   Building action repertoires: Memory and learning functions of the basal ganglia [J].
Graybiel, AM .
CURRENT OPINION IN NEUROBIOLOGY, 1995, 5 (06) :733-741
[25]   NERVE GROWTH-FACTOR EFFECTS ON CHOLINERGIC NEURONS OF NEOSTRIATUM AND NUCLEUS ACCUMBENS IN THE ADULT-RAT [J].
HAGG, T ;
HAGG, F ;
VAHLSING, HL ;
MANTHORPE, M ;
VARON, S .
NEUROSCIENCE, 1989, 30 (01) :95-103
[26]   GENERATION AND MIGRATION OF CELLS IN THE DEVELOPING STRIATUM [J].
HALLIDAY, AL ;
CEPKO, CL .
NEURON, 1992, 9 (01) :15-26
[27]   Functions of LIM-homeobox genes [J].
Hobert, O ;
Westphal, H .
TRENDS IN GENETICS, 2000, 16 (02) :75-83
[28]  
Hobert O, 1999, DEVELOPMENT, V126, P1547
[29]   Regulation of interneuron function in the C-elegans thermoregulatory pathway by the ttx-3 LIM homeobox gene [J].
Hobert, O ;
Mori, I ;
Yamashita, Y ;
Honda, H ;
Ohshima, Y ;
Liu, YX ;
Ruvkun, G .
NEURON, 1997, 19 (02) :345-357
[30]  
Hobert O, 1998, J NEUROSCI, V18, P2084