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K562 erythroid and HL60 macrophage differentiation downregulates polycystin, a large membrane-associated protein.

作者信息

Aguiari G, Piva R, Manzati E, Mazzoni E, Augello G, Chiari E, Moretti S, Neri L M, del Senno L

机构信息

Dipartimento di Morfologia ed Embriologia, Universitá degli Studi, Ferrara, Italy.

出版信息

Exp Cell Res. 1998 Oct 10;244(1):259-67. doi: 10.1006/excr.1998.4198.

DOI:10.1006/excr.1998.4198
PMID:9770368
Abstract

Polycystin, the PKD1 gene product mutated in autosomal dominant polycystic kidney disease, is a large membrane protein which is important in the differentiation of epithelial tubular structure. Furthermore, PKD1 mRNA is expressed in various tissues and in neoplastic cell lines particularly, suggesting that polycystin might be involved in differentiation and/or proliferation of other cell types. Therefore, in order to investigate such a possible role, polyclonal antibodies against a recombinant polycystin peptide were raised and used to study polycystin expression in human leukemia cell lines committed to differentiation. Using Western blot and laser scanning confocal microscopy analyses, we demonstrated expression of polycystin in erythroleukemia K562 cells as a membrane-associated polypeptide of approximately 450 kDa, mainly localized in cell-cell contacts. Protein size and subcellular distribution were similar to those found in the kidney epithelial KJ29 cell line. In addition, K562 cell erythroid differentiation induced by hemin was characterized by a reduction in polycystin expression, as measured by Western blot and Northern blot analyses. Cytofluorimetric analysis indicated that upon hemin treatment there was a progressive reduction in the number of polycystin-expressing cells as well as in proliferation rate. Furthermore, reduction in proliferating and polycystin-expressing cells was also observed in K562 cells after serum starvation. When serum was added to the serum-deprived cells an increase in cell number as well as in number of polycystin-positive cells was observed. In addition, polycystin, also expressed in promyelocytic leukemia HL60 cells, was downregulated when macrophage differentiation in HL60 was induced by TPA. Therefore, in these leukemic cells downregulation of polycystin appeared to be closely related to reduction in cell proliferation and to induction of differentiation. This suggests that polycystin may play a relevant role in these cell processes.

摘要

相似文献

1
K562 erythroid and HL60 macrophage differentiation downregulates polycystin, a large membrane-associated protein.
Exp Cell Res. 1998 Oct 10;244(1):259-67. doi: 10.1006/excr.1998.4198.
2
The PKD1 gene product, "polycystin-1," is a tyrosine-phosphorylated protein that colocalizes with alpha2beta1-integrin in focal clusters in adherent renal epithelia.多囊肾病1基因(PKD1)的产物“多囊蛋白-1”是一种酪氨酸磷酸化蛋白,它与α2β1整合素在贴壁肾上皮细胞的局灶性簇中共同定位。
Lab Invest. 1999 Oct;79(10):1311-23.
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Transmembrane domain analysis of polycystin-1, the product of the polycystic kidney disease-1 (PKD1) gene: evidence for 11 membrane-spanning domains.多囊肾病1(PKD1)基因产物多囊蛋白-1的跨膜结构域分析:11个跨膜结构域的证据。
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Co-assembly of polycystin-1 and -2 produces unique cation-permeable currents.多囊蛋白-1和-2的共同组装产生独特的阳离子通透电流。
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Adult, fetal, and polycystic kidney expression of polycystin, the polycystic kidney disease-1 gene product.多囊蛋白(多囊肾病-1基因产物)在成人、胎儿及多囊肾中的表达
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Cellular localization and tissue distribution of polycystin-1.多囊蛋白-1的细胞定位与组织分布
J Pathol. 1999 Aug;188(4):439-46. doi: 10.1002/(SICI)1096-9896(199908)188:4<439::AID-PATH367>3.0.CO;2-P.
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Biochemical characterization of bona fide polycystin-1 in vitro and in vivo.
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Genes homologous to the autosomal dominant polycystic kidney disease genes (PKD1 and PKD2).与常染色体显性多囊肾病基因(PKD1和PKD2)同源的基因。
Eur J Hum Genet. 1999 Dec;7(8):860-72. doi: 10.1038/sj.ejhg.5200383.
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Depletion of PKD1 by an antisense oligodeoxynucleotide induces premature G1/S-phase transition.反义寡脱氧核苷酸使多囊蛋白-1缺失会诱导细胞提前从G1期过渡到S期。
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10
K562 erythroleukemia cells express cytokeratins 8, 18, and 19 and epithelial membrane antigen that disappear after induced differentiation.
J Cell Physiol. 1990 May;143(2):310-20. doi: 10.1002/jcp.1041430215.

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