Constitutive expression of Mpl ligand transcripts during thrombocytopenia or thrombocytosis

被引:96
作者
CohenSolal, K [1 ]
Villeval, JL [1 ]
Titeux, M [1 ]
Lok, S [1 ]
Vainchenker, W [1 ]
Wendling, F [1 ]
机构
[1] ZYMOGENET INC, SEATTLE, WA USA
关键词
D O I
10.1182/blood.V88.7.2578.bloodjournal8872578
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Mpl ligand (thrombopoietin [TPO]) is the physiological regulator of platelet production, In mice, mRNA encoding the Mpl ligand (Mpl-L) is predominantly found by Northern blot analysis in the liver and kidney, To investigate the mode of regulation of the Mpl-L gene, we have developed several experimental models of severe thrombocytopenia differing in their kinetics and an opposite model of chronic thrombocytosis. Northern analysis performed at various times after induction of a thrombocytopenic state demonstrates that, whatever the number of circulating platelets, no change in Mpl-L mRNA level occurs in liver and kidney. By ribonuclease protection assays, we analyzed the ratios between mRNAs coding for the wild-type Mpl-L form and various splice variants encoding inactive or nonsecreted Mpl-L proteins, No modification in levels of these various isoforms was detected confirming the data of a previous report, Because the highest level of Mpl-L bioactivity in sera was observed only in mice with drastically reduced numbers of both platelets and megakaryocytes, these results further suggest that not only platelets, but also megakaryocytes, must be involved in the regulation of the level of circulating Mpl-L, In addition, we show that no downregulation of wild-type Mpl-L mRNA and no change in the ratio of Mpl-L mRNA isoforms were detected in mice in which a chronic thrombocytosis was induced, Together, these different models extend and further confirm that the regulation of Mpl-L does not occur at a transcriptional level or by a modulation in the ratios of Mpl-L mRNA isoforms. (C) 1996 by The American Society of Hematology.
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页码:2578 / 2584
页数:7
相关论文
共 35 条
[1]   Deficiencies in progenitor cells of multiple hematopoietic lineages and defective megakaryocytopoiesis in mice lacking the thrombopoietin receptor c-mpl [J].
Alexander, WS ;
Roberts, AW ;
Nicola, NA ;
Li, RL ;
Metcalf, D .
BLOOD, 1996, 87 (06) :2162-2170
[2]   IDENTIFICATION AND CLONING OF A MEGAKARYOCYTE GROWTH AND DEVELOPMENT FACTOR THAT IS A LIGAND FOR THE CYTOKINE RECEPTOR MPL [J].
BARTLEY, TD ;
BOGENBERGER, J ;
HUNT, P ;
LI, YS ;
LU, HS ;
MARTIN, F ;
CHANG, MS ;
SAMAL, B ;
NICHOL, JL ;
SWIFT, S ;
JOHNSON, MJ ;
HSU, RY ;
PARKER, VP ;
SUGGS, S ;
SKRINE, JD ;
MEREWETHER, LA ;
CLOGSTON, C ;
HSU, E ;
HOKOM, MM ;
HORNKOHL, A ;
CHOI, E ;
PANGELINAN, M ;
SUN, Y ;
MAR, V ;
MCNINCH, J ;
SIMONET, L ;
JACOBSEN, F ;
XIE, C ;
SHUTTER, J ;
CHUTE, H ;
BASU, R ;
SELANDER, L ;
TROLLINGER, D ;
SIEU, L ;
PADILLA, D ;
TRAIL, G ;
ELLIOTT, G ;
IZUMI, R ;
COVEY, T ;
CROUSE, J ;
GARCIA, A ;
XU, W ;
DELCASTILLO, J ;
BIRON, J ;
COLE, S ;
HU, MCT ;
PACIFICI, R ;
PONTING, I ;
SARIS, C ;
WEN, D .
CELL, 1994, 77 (07) :1117-1124
[3]   MACROPHAGES SPECIFICALLY REGULATE THE CONCENTRATION OF THEIR OWN GROWTH-FACTOR IN THE CIRCULATION [J].
BARTOCCI, A ;
MASTROGIANNIS, DS ;
MIGLIORATI, G ;
STOCKERT, RJ ;
WOLKOFF, AW ;
STANLEY, ER .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (17) :6179-6183
[4]   ANEMIA INDUCES ACCUMULATION OF ERYTHROPOIETIN MESSENGER-RNA IN THE KIDNEY AND LIVER [J].
BONDURANT, MC ;
KOURY, MJ .
MOLECULAR AND CELLULAR BIOLOGY, 1986, 6 (07) :2731-2733
[5]   THROMBOPOIETIN (C-MPL LIGAND) ACTS SYNERGISTICALLY WITH ERYTHROPOIETIN, STEM-CELL FACTOR, AND INTERLEUKIN-11 TO ENHANCE MURINE MEGAKARYOCYTE COLONY GROWTH AND INCREASES MEGAKARYOCYTE PLOIDY IN-VITRO [J].
BROUDY, VC ;
LIN, NL ;
KAUSHANSKY, K .
BLOOD, 1995, 85 (07) :1719-1726
[6]   CLONING AND CHARACTERIZATION OF THE HUMAN MEGAKARYOCYTE GROWTH AND DEVELOPMENT FACTOR (MGDF) GENE [J].
CHANG, MS ;
MCNINCH, J ;
BASU, R ;
SHUTTER, J ;
HSU, RY ;
PERKINS, C ;
MAR, V ;
SUGGS, S ;
WELCHER, A ;
LI, L ;
LU, H ;
BARTLEY, T ;
HUNT, P ;
MARTIN, F ;
SAMAL, B ;
BOGENBERGER, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (02) :511-514
[7]   SINGLE-STEP METHOD OF RNA ISOLATION BY ACID GUANIDINIUM THIOCYANATE PHENOL CHLOROFORM EXTRACTION [J].
CHOMCZYNSKI, P ;
SACCHI, N .
ANALYTICAL BIOCHEMISTRY, 1987, 162 (01) :156-159
[8]   THE MPI RECEPTOR IS EXPRESSED IN THE MEGAKARYOCYTIC LINEAGE FROM LATE PROGENITORS TO PLATELETS [J].
DEBILI, N ;
WENDLING, F ;
COSMAN, D ;
TITEUX, M ;
FLORINDO, C ;
DUSANTERFOURT, I ;
SCHOOLEY, K ;
METHIA, N ;
CHARON, M ;
NADOR, R ;
BETTAIEB, A ;
VAINCHENKER, W .
BLOOD, 1995, 85 (02) :391-401
[9]   STIMULATION OF MEGAKARYOCYTOPOIESIS AND THROMBOPOIESIS BY THE C-MPL LIGAND [J].
DESAUVAGE, FJ ;
HASS, PE ;
SPENCER, SD ;
MALLOY, BE ;
GURNEY, AL ;
SPENCER, SA ;
DARBONNE, WC ;
HENZEL, WJ ;
WONG, SC ;
KUANG, WJ ;
OLES, KJ ;
HULTGREN, B ;
SOLBERG, LA ;
GOEDDEL, DV ;
EATON, DL .
NATURE, 1994, 369 (6481) :533-538
[10]   Physiological regulation of early and late stages of megakaryocytopoiesis by thrombopoietin [J].
deSauvage, FJ ;
CarverMoore, K ;
Luoh, SM ;
Ryan, A ;
Dowd, M ;
Eaton, DL ;
Moore, MW .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 183 (02) :651-656