Diverse gene expression and function of semaphorins in developing lung: positive and negative regulatory roles of semaphorins in lung branching morphogenesis

被引:81
作者
Kagoshima, M
Ito, T
Kitamura, H
Goshima, Y
机构
[1] Yokohama City Univ, Sch Med, Dept Pharmacol, Kanazawa Ku, Yokohama, Kanagawa 2360004, Japan
[2] Yokohama City Univ, Sch Med, Dept Pathol, Kanazawa Ku, Yokohama, Kanagawa 2360004, Japan
[3] JST, CREST, Kawaguchi, Saitama 3320012, Japan
关键词
D O I
10.1046/j.1365-2443.2001.00441.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Background: Previously, we reported that Sema3A, one of the secreted repulsive axon guidance molecules, CRMP (collaprin response mediator protein)-2, a putative intracellular signalling molecule for Sema3A and Sema3A receptor neuropilin-1 are expressed in the developing lung. Sema3A inhibits branching morphogenesis of embryonic lung in organ culture. Results: We examined the gene expression of Sema3A, Sema3C, Sema3F and their receptors, NP-1, NP-2 and plexin-A1 by in situ hybridization. Transcripts of all six genes were detected in mouse lung from embryonic day E11.5 to E17.5, acid displayed highly specific spatiotemporal distributions, The distribution of the receptor genes was detected in patterns which were consistent with known receptor usage of the semaphorins, In contrast to Sema3A, we found that the other class 3 semaphorins, Sema3C and Sema3F, stimulated branching morphogenesis. This stimulatory effect of Sema3C or Sema3F was accompanied by a moderate increase in the incorporation of bromodeoxyuridine (BrdU) into DNA in the terminal epithelial cells. Conclusion: The coordinated expression patterns of different semaphorins and their receptors, together with the specific activities affecting branching morphogenesis, suggest that the semaphorins act as both positive and negative regulators of branching morphogenesis in the developing lung.
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页码:559 / 571
页数:13
相关论文
共 48 条
[1]   The chemorepulsive activity of secreted semaphorins is regulated by furin-dependent proteolytic processing [J].
Adams, RH ;
Lohrum, M ;
Klostermann, A ;
Betz, H ;
Puschel, AW .
EMBO JOURNAL, 1997, 16 (20) :6077-6086
[2]  
Bagnard D, 1998, DEVELOPMENT, V125, P5043
[3]  
Bellusci S, 1996, DEVELOPMENT, V122, P1693
[4]  
Cardoso WV, 2000, DEV DYNAM, V219, P121, DOI 10.1002/1097-0177(2000)9999:9999<::AID-DVDY1053>3.3.CO
[5]  
2-8
[6]  
Chédotal A, 1998, DEVELOPMENT, V125, P4313
[7]   Neuropilin-2, a novel member of the neuropilin family, is a high affinity receptor for the semaphorins Sema E and Sema IV but not Sema III [J].
Chen, H ;
Chedotal, A ;
He, ZG ;
Goodman, CS ;
TessierLavigne, M .
NEURON, 1997, 19 (03) :547-559
[8]   Neuropilin-2 regulates the development of select cranial and sensory nerves and hippocampal mossy fiber projections [J].
Chen, H ;
Bagri, A ;
Zupicich, JA ;
Zou, YM ;
Stoeckli, E ;
Pleasure, SJ ;
Lowenstein, DH ;
Skarnes, WC ;
Chédotal, A ;
Tessier-Lavigne, M .
NEURON, 2000, 25 (01) :43-56
[9]   A poxvirus-encoded semaphorin induces cytokine production from monocytes and binds to a novel cellular semaphorin receptor, VESPR [J].
Comeau, MR ;
Johnson, R ;
DuBose, RF ;
Petersen, M ;
Gearing, P ;
VandenBos, T ;
Park, L ;
Farrah, T ;
Buller, RM ;
Cohen, JI ;
Strockbine, LD ;
Rauch, C ;
Spriggs, MK .
IMMUNITY, 1998, 8 (04) :473-482
[10]  
de Castro F, 1999, J NEUROSCI, V19, P4428