A designer hyper interleukin 11 (H11) is a biologically active cytokine

被引:35
作者
Dams-Kozlowska, Hanna [1 ,2 ]
Gryska, Katarzyna [2 ]
Kwiatkowska-Borowczyk, Eliza [1 ,2 ]
Izycki, Dariusz [2 ]
Rose-John, Stefan [3 ]
Mackiewicz, Andrzej [1 ,2 ]
机构
[1] Greater Poland Canc Ctr, Dept Canc Diagnost & Immunol, PL-61866 Poznan, Poland
[2] Poznan Univ Med Sci, Chair Med Biotechnol, Poznan, Poland
[3] Univ Kiel, Dept Biochem, Kiel, Germany
关键词
IL-11; sIL-11R alpha; Hyper-IL11; Fusion protein; gp130; targeting; Hypercytokine; RECEPTOR ALPHA-CHAIN; FUSION PROTEIN; IL-11; RECEPTOR; GP130; COMPLEX; CELLS; EXPRESSION; BIOLOGY; BINDING; DOMAIN;
D O I
10.1186/1472-6750-12-8
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 [微生物学]; 090105 [作物生产系统与生态工程];
摘要
Background: Interleukin 11 (IL-11) is a pleiotropic cytokine with anti-apoptotic, anti-inflammatory and hematopoietic potential. The IL-11 activity is determined by the expression of the IL-11R receptor alpha (IL-11R alpha) and the signal transducing subunit beta (gp130) on the cell membrane. A recombinant soluble form of the IL-11R alpha (sIL-11R alpha) in combination with IL-11 acts as an agonist on cells expressing the gp130 molecule. We constructed a designer cytokine Hyper IL-11 (H11), which is exclusively composed of naturally existing components. It contains the full length sIL-11R alpha connected with the mature IL-11 protein using their natural sequences only. Such a construct has two major advantages: (i) its components are as close as possible to the natural forms of both proteins and (ii) it lacks an artificial linker what should avoid induction of antibody production. Results: The H11 construct was generated, the protein was produced in a baculovirus expression system and was then purified by using ion exchange chromatography. The H11 protein displayed activity in three independent bioassays, (i) it induced acute phase proteins production in HepG2 cells expressing IL-11, IL-11R alpha and gp130, (ii) it stimulated the proliferation of B9 cells (cells expressing IL-11R alpha and gp130) and (iii) proliferation of Baf/ 3-gp130 cells (cells not expressing IL-11 and IL-11R alpha but gp130). Moreover, the preliminary data indicated that H11 was functionally distinct from Hyper-IL-6, a molecule which utilizes the same homodimer of signal transducing receptor (gp130). Conclusions: The biologically active H11 may be potentially useful for treatment of thrombocytopenia, infertility, multiple sclerosis, cardiovascular diseases or inflammatory disorders.
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页数:11
相关论文
共 31 条
[1]
Interleukin-11 signals through the formation of a hexameric receptor complex [J].
Barton, VA ;
Hall, MA ;
Hudson, KR ;
Heath, JK .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (46) :36197-36203
[2]
Delivering new insight into the biology of megakaryopoiesis and thrombopoiesis [J].
Battinelli, Elisabeth M. ;
Hartwig, John H. ;
Italiano, Joseph E., Jr. .
CURRENT OPINION IN HEMATOLOGY, 2007, 14 (05) :419-426
[3]
Baumann H, 1996, J IMMUNOL, V157, P284
[4]
Interleukin-6 family of cytokines induced activation of different functional sites expressed by gp130 transducing protein [J].
Chevalier, S ;
Fourcin, M ;
Robledo, O ;
Wijdenes, J ;
PouplardBarthelaix, A ;
Gascan, H .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (25) :14764-14772
[5]
Structure of an extracellular gp130 cytokine receptor signaling complex [J].
Chow, DC ;
He, XL ;
Snow, AL ;
Rose-John, S ;
Garcia, KC .
SCIENCE, 2001, 291 (5511) :2150-2155
[6]
Recombinant soluble interleukin-11 (IL-11) receptor alpha-chain can act as an IL-11 antagonist [J].
Curtis, DJ ;
Hilton, DJ ;
Roberts, B ;
Murray, L ;
Nicola, N ;
Begley, CG .
BLOOD, 1997, 90 (11) :4403-4412
[7]
Dams-Kozlowska H, 2001, ADV EXP MED BIOL, V495, P373
[8]
Interleukin-11: Review of molecular, cell biology, and clinical use [J].
Du, XX ;
Williams, DA .
BLOOD, 1997, 89 (11) :3897-3908
[9]
Conditional gp130 deficient mouse mutants [J].
Fasnacht, Nicolas ;
Mueller, Werner .
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 2008, 19 (04) :379-384
[10]
A bioactive designer cytokine for human hematopoietic progenitor cell expansion [J].
Fischer, M ;
Goldschmitt, J ;
Peschel, C ;
Brakenhoff, JPG ;
Kallen, KJ ;
Wollmer, A ;
Grotzinger, J ;
RoseJohn, S .
NATURE BIOTECHNOLOGY, 1997, 15 (02) :142-145