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Molecular Cloning and Expression of Megakaryocyte Potentiating Factor cDNA

1995; Elsevier BV; Volume: 270; Issue: 37 Linguagem: Inglês

10.1074/jbc.270.37.21984

1083-351X

Tetsuo Kojima, Masayoshi Oh‐eda, Kunihiro Hattori, Yoshiko Taniguchi, Masahiko Tamura, Norimichi Ochi, Nozomi Yamaguchi,

Neuropeptides and Animal Physiology

The human megakaryocyte potentiating factor (hMPF) has been previously purified from a culture supernatant of human pancreatic cancer cells HPC-Y5 (Yamaguchi, N., Hattori, K., Oh-eda, M., Kojima, T., Imai, N., and Ochi, N.(1994) J. Biol. Chem. 269, 805-808). We have now isolated hMPF cDNA from a HPC-Y5 cDNA library using polymerase chain reaction and plaque hybridization methods. The hMPF cDNA encodes a polypeptide consisting of 622 amino acids, including a signal peptide of 33 amino acids, and with a deduced molecular mass of 68 kDa, although HPC-Y5 cells secrete a 33-kDa form of hMPF. Human MPF does not show any significant homology with other previously described sequences. The cDNA was expressed in COS-7 and Chinese hamster ovary (CHO) cells, and megakaryocyte potentiating activity was detected in their culture supernatant. The COS-7 cells secreted only a 33-kDa recombinant hMPF, whereas an additional 30-kDa form was detected in the culture medium of CHO cells. The 33-kDa rhMPF purified from CHO cells showed megakaryocyte potentiating activity, but not the purified 30-kDa rhMPF. The difference in structure and activity between the 33- and 30-kDa forms of hMPF was ascribed to the existence in the 33-kDa form of the C-terminal 25 amino acid residues. The human megakaryocyte potentiating factor (hMPF) has been previously purified from a culture supernatant of human pancreatic cancer cells HPC-Y5 (Yamaguchi, N., Hattori, K., Oh-eda, M., Kojima, T., Imai, N., and Ochi, N.(1994) J. Biol. Chem. 269, 805-808). We have now isolated hMPF cDNA from a HPC-Y5 cDNA library using polymerase chain reaction and plaque hybridization methods. The hMPF cDNA encodes a polypeptide consisting of 622 amino acids, including a signal peptide of 33 amino acids, and with a deduced molecular mass of 68 kDa, although HPC-Y5 cells secrete a 33-kDa form of hMPF. Human MPF does not show any significant homology with other previously described sequences. The cDNA was expressed in COS-7 and Chinese hamster ovary (CHO) cells, and megakaryocyte potentiating activity was detected in their culture supernatant. The COS-7 cells secreted only a 33-kDa recombinant hMPF, whereas an additional 30-kDa form was detected in the culture medium of CHO cells. The 33-kDa rhMPF purified from CHO cells showed megakaryocyte potentiating activity, but not the purified 30-kDa rhMPF. The difference in structure and activity between the 33- and 30-kDa forms of hMPF was ascribed to the existence in the 33-kDa form of the C-terminal 25 amino acid residues. INTRODUCTIONMegakaryocytes originate from pluripotent hematopoietic stem cells through a complex process involving commitment of the pluripotent hematopoietic progenitor to megakaryocytic precursor cells and their mitotic amplification. The regulatory system governing megakaryocytopoiesis and platelet production is thought to take place in at least two stages, 1) during proliferation and differentiation of megakaryocytic progenitor cells, leading to the production of megakaryocytes, and 2) during maturation of megakaryocytes which leads to the production of platelets. Megakaryocyte proliferation is thought to be dependent on an essential megakaryocyte colony-stimulating factor, and this proliferation can be potentiated in vitro by ancillary megakaryocyte potentiators (Meg-POT) 1The abbreviations used are: Meg-POTmegakaryocyte potentiatorMPFmegakaryocyte potentiating factorPCRpolymerase chain reactionhhumanCHOChinese hamster ovaryFCSfetal calf serumHPLChigh performance liquid chromatographyPAGEpolyacrylamide gel electrophoresisILinterleukin. (1Williams N. Eger R.R. Jackson H.M. Nelson D.J. J. Cell. Physiol. 1982; 110: 101-104Crossref PubMed Scopus (117) Google Scholar, 2Gordon M.S. Hoffman R. Blood. 1992; 80: 302-307Crossref PubMed Google Scholar, 3Williams N. Jackson H. Ralph P. Nakoinz I. Blood. 1981; 57: 157-163Crossref PubMed Google Scholar), which also stimulate the maturation of the megakaryocytes. We have recently identified, in the culture supernatant of the human pancreatic cancer cells HPC-Y5, a novel megakaryocyte potentiating factor (hMPF), which stimulates the megakaryocyte colony forming activity of murine interleukin-3 in mouse bone marrow cell culture(4Yamaguchi N. Hattori K. Oh-eda M. Kojima T. Imai N. Ochi N. J. Biol. Chem. 1994; 269: 805-808Abstract Full Text PDF PubMed Google Scholar). The factor was found to consist of a single polypeptide of about 32 kDa with at least one N-linked sugar chain. In this paper, we describe the molecular cloning and characterization of the cDNA encoding human MPF.MATERIALS AND METHODSProtein and Amino Acid Sequence DeterminationHuman MPF was purified from HPC-Y5 culture supernatant as described previously (4Yamaguchi N. Hattori K. Oh-eda M. Kojima T. Imai N. Ochi N. J. Biol. Chem. 1994; 269: 805-808Abstract Full Text PDF PubMed Google Scholar) and partially digested with endoproteinase Glu-C (Boehringer-Mannheim) in the presence of 10 mM 2-mercaptoethanol and 2 M urea at 37°C for 18 h. Peptide fragments were then separated on a Vydac C18 reverse-phase column, and subjected, with purified MPF, to sequence analysis in an Applied Biosystems model 473A or 476A protein sequencer.cDNA Library (I) and Polymerase Chain Reaction (PCR)Total RNA was prepared from HPC-Y5 cells(5Chirgwin J.M. Przybyla A.E. MacDonald R.J. Rutter W.J. Biochemistry. 1979; 18: 5294-5299Crossref PubMed Scopus (16619) Google Scholar), and poly(A)+ RNA was further purified by oligo(dT)-cellulose chromatography. Complementary DNA was synthesized by oligo(dT) priming and inserted into λZAPII phage vector (Stratagene). After one round of amplification of the resulting cDNA library (106 independent clones), the DNA was extracted, and an aliquot (500 ng) was subjected to PCR in the presence of 50 pmol of each forward and backward primers and 1.25 units of Taq DNA polymerase (Perkin-Elmer). The DNA was denaturated at 95°C for 7 min, and PCR was carried out for 40 cycles as follows: annealing at 60°C for 1 min, extension at 72°C for 2 min, and denaturation at 94°C for 1 min. An aliquot (1/20) of the PCR products was subjected to a second PCR with inner primers. The PCR products were separated on polyacrylamide gel, and the desired DNA fragment was excised, purified, and subcloned into a pSP73 vector (Promega) for sequencing.cDNA Library (II) and ScreeningA second HPC-Y5 cDNA library was used for isolating a full-length cDNA. Complementary DNA was synthesized as above(6Gubler U. Hoffman B.J. Gene (Amst.). 1983; 25: 263-269Crossref PubMed Scopus (3066) Google Scholar), inserted into the UniZAP XR directional cloning vector (Stratagene), and packaged into λ phage using Gigapack Gold (Stratagene), thus yielding 1.8 × 106 independent clones.In order to isolate a full-length hMPF cDNA, approximately 1.7 × 106 clones were screened with Q197A(7Benton W.D. Davis R.W. Science. 1977; 196: 180-182Crossref PubMed Scopus (2922) Google Scholar), a 197-base pair MPF cDNA fragment generated by PCR. This fragment was labeled by 32P using a Random Primer Labeling kit (TAKARA) in the presence of QS and AA primers instead of the kit's random primers, and used as hybridization probe. Filters (Hybond N+, Amersham) were hybridized with the 32P-labeled Q197A probe. Isolated clones were subjected to in vivo excision of pBluescript SK(-) phagemid (Stratagene), and plasmid DNA was prepared by the standard method.DNA SequencingDNA sequences were determined using Sequenase version 2.0 (U. S. Biochemical Corp.) and appropriate synthetic oligonucleotide primers.Antibody PreparationThe XhoI fragment of MPF cDNA (nucleotides 181-2109) was excised from pKPO27, and inserted into the StuI site of a pMAL-c Escherichia coli (E. coli) expression vector (New England BioLabs), in which hMPF is expressed as a fusion protein with maltose-binding protein. This fusion protein was purified according to the manufacturer's protocol, and used for immunization. Rabbits or BALB/c mice were immunized five times at 2-week intervals with rhMPF emulsified with complete Freund's adjuvant. Rabbit anti-MPF plasma was collected 10 days after the final injection. Mouse splenocytes were isolated 9 days after the final injection, and fused to P3U1 mouse myeloma cells to establish hybridomas.Expression of hMPF cDNA in COS-7 CellsPlasmid pRVHKPO27f, harboring the MPF cDNA downstream of the human elongation factor 1α (8Mizushima S. Nagata S. Nucleic Acids Res. 1990; 18: 5322Crossref PubMed Scopus (1498) Google Scholar) promoter, was constructed from pKPO27 and HEF-12 h-Gγ1(9Bendig, M. M., Jones, S. T., Saldanha, J. W., Sato, K., Tsuchiya, M., Sato, K., (April 24, 1992) International Patent Application WO 92-19759.Google Scholar), which includes the simian virus 40 (SV40) origin site. The plasmid (10 μg) was introduced by electroporation (1900 V, 25 microfarads, Bio-Rad Gene Pulser) into COS-7 cells suspended in phosphate-buffered saline at a density of 1 × 107 cells/ml. Transformants were cultured in Dulbecco's minimum essential medium containing 1% fetal calf serum (FCS) at 37°C under 5% CO2 for 72 h.Establishment of rhMPF-producing CHO Cell line (FKL5F)Plasmid pEFDKPO27f, harboring the mouse dihydrofolate reductase (DHFR) cDNA downstream of the SV40 early promoter and hMPF cDNA downstream of the elongation factor 1α promoter, was constructed from DHFR-ΔE-RVh(9Bendig, M. M., Jones, S. T., Saldanha, J. W., Sato, K., Tsuchiya, M., Sato, K., (April 24, 1992) International Patent Application WO 92-19759.Google Scholar), pCDM8(10Seed B. Nature. 1987; 329: 840-842Crossref PubMed Scopus (486) Google Scholar), and pKPO27. Dihydrofolate reductase-deficient CHO cells (DXB-11) were cultured in α-minimum essential medium, supplemented with 10% FCS, and transfected with linearized pEFDKPO27f. Transformants were selected in nucleoside-free minimal essential medium supplemented with 10% FCS, and the introduced genes were amplified by stepwise addition of methotrexate (Sigma). Human MPF concentration in the culture supernatant of the transfected CHO (FKL5F) cells was determined by enzyme-linked immunosorbent assay. FKL5F cells which exhibited the highest productivity were propagated in Iscove's modified Dulbecco's medium containing 10 nM methotrexate and 2% FCS.Purification of rhMPF Produced in CHO CellsFor the purification of 33-kDa MPF, the cell culture supernatant (10 liters) was filtrated through a 5-μm membrane (Amicon, Inc.) to remove cellular debris. The filtrate was then applied to a Blue Sepharose Fast Flow column (5 × 20 cm, Pharmacia) equilibrated with 50 mM Tris-HCl (pH 8.0) containing 0.2 M NaCl and 0.01% Tween 20. The column was washed with the same buffer, and proteins were eluted with 2 M KCl in 50 mM Tris-HCl (pH 9.0) containing 0.01% Tween 20. The eluate was desalted by repeated concentrations and dilutions, the resulting concentrate centrifuged (10,000 × g, 30 min), and the supernatant was applied to an S-Sepharose Fast Flow column (5 × 12 cm, Pharmacia) equilibrated with 20 mM sodium acetate buffer (pH 5.0) containing 0.01% Tween 20. The column was washed with the same buffer, and proteins were eluted stepwise with a NaCl gradient (0.1, 0.2, 0.3, 0.5, and 1.0 M) in equilibration buffer. The fraction containing MPF was applied to a reverse-phase HPLC column (C4, 20 × 250 mm, Vydac) equilibrated with 24% acetonitrile in 0.1% trifluoroacetic acid. The column was washed with the same solvent, and proteins were eluted with a 24-48% linear gradient of acetonitrile in 0.1% trifluoroacetic acid for 48 min at a flow rate of 2 ml/min. MPF fractions were pooled and applied to a TSKgel G3000SW column (21.5 × 600 mm, TOSOH) equilibrated with 40% acetonitrile in 0.1% trifluoroacetic acid, and the column was developed with the same solvent at a flow rate of 3 ml/min. The MPF fraction was applied to a reverse-phase HPLC column (10 × 250 mm, Vydac) at a flow rate of 1 ml/min, and MPF was eluted with a linear gradient of acetonitrile as described above.For 30-kDa MPF purification, the cell culture supernatant was filtrated, concentrated, and MPF was precipitated at 4°C with ammonium sulfate at 50% saturation. The precipitate was dissolved in 10 mM Tris-HCl (pH 7.4) containing 1 M ammonium sulfate, and applied to a Phenyl-Sepharose Fast Flow column (5 × 15 cm) equilibrated with the same buffer. MPF was eluted with 10 mM Tris-HCl (pH 8.5) containing 0.1% Tween 20. The 30-kDa MPF was further purified by a combination of reverse-phase HPLC and TSK G3000SW gel permeation chromatography as described above. Fractions containing MPF were identified by Western blotting at each step of the purification.C-terminal Amino Acid SequencePurified recombinant MPF was cleaved with cyanogen bromide. C-terminal peptides were separated by reverse-phase HPLC on a Vydac C18 column (4.6 × 250 mm). The large C-terminal peptide was digested with endoproteinase Asp-N (Boehringer Mannheim), and the resulting peptides were fractionated as described above.Northern (RNA) Blot AnalysisHuman Multiple Tissue Northern blot was obtained from Clontech and membranes were hybridized with the radiolabeled MPF cDNA.Megakaryocyte Colony-forming AssayUnfractionated bone marrow cells (2 × 105) from C57BL/6N mice were cultured in 1 ml of modified McCoy's 5A medium (Life Technologies, Inc.) supplemented with 20% horse serum (Biocell) and containing 0.3% agar, according to the method of Metcalf(11Metcalf D. MacDonald H.R. Odartchenko N. Sordat B. Proc. Natl. Acad. Sci. U. S. A. 1975; 72: 1744-1748Crossref PubMed Scopus (166) Google Scholar). The number of megakaryocyte colonies formed after 6 days of culture in the presence of 1 ng/ml mouse recombinant IL-3 was determined by acetylcholine esterase staining of the dehydrated culture. Colonies containing more than 4 cells were scored.RESULTSProtein Sequencing of Natural MPFThe N-terminal amino acid sequence of natural MPF purified from HPC-Y5 culture supernatant was determined to be Leu-Ala-Gly-Glu-Thr-Gly-Gln-Glu-Ala-Ala-Pro-Leu-Asp-Gly-Val-Leu-Ala-Asn as previously reported(4Yamaguchi N. Hattori K. Oh-eda M. Kojima T. Imai N. Ochi N. J. Biol. Chem. 1994; 269: 805-808Abstract Full Text PDF PubMed Google Scholar). Purified natural MPF was partially digested with endoproteinase Glu-C, to obtain large fragments for the determination of the MPF internal amino acid sequences. One of the amino acid sequences of the fragments was Ala-Gln-LysAsn-Val-Lys-Leu-Ser-Thr-Glu-Gln-Leu-Arg-Cys-Leu-Ala-HisArg-Leu-Ser-Glu-Pro-Pro-Glu-Asp-Leu-Asp-Ala.Isolation of MPF cDNA ClonesThree relatively low degenerated oligonucleotides (N1, K4S, and K4A) corresponding to the underlined amino acid sequences shown above were synthesized as shown in Fig. 1 and used as primers for PCR amplification of a MPF cDNA segment. A fragment of the expected size (84 base pairs) was obtained from the HPC-Y5 cDNA library after 2 rounds of PCR amplification, as described in Fig. 1A, first in the presence of T7 promoter sequence and N1 primer, then in the presence of the inner primers K4S and K4A. The sequence of this fragment subcloned in pSP73 vector was 5′-CTCTCAACAGAGCAGCTGCGCTGTCTGGCTCACCGGCTCTCTGA-3′ (not including the primers). The deduced amino acid sequence encoded by this PCR-amplified fragment and that of the peptide obtained by endopeptidase Glu-C digestion were found to be identical. Using four synthetic primers on the basis of this sequence information, a 197-base pair fragment Q197A was generated by repeated PCR amplification, as shown in Fig. 1A. Its nucleotide sequence was found to encode the amino acid sequence of a part of MPF, demonstrating that Q197A is a fragment of MPF cDNA.Twenty-three positive clones were isolated from the cDNA library (II) (1.7 × 106) by plaque hybridization using the Q197A fragment as a probe. One of them, clone pKPO27, was subjected to further analysis, since it contained the longest insert.Structure of MPF cDNAFig. 2 shows the entire nucleotide sequence of the cDNA insert of pKPO27. To confirm this sequence, another positive clone pKPO32 was analyzed, and no difference was found in the overlapping cDNA regions of pKPO27 and pKPO32. The cDNA contains a single long open reading frame of 1869 nucleotides, with a potential polyadenylation sequence AGTAAA just upstream of the poly(A) tail. Structure analysis showed that the first ATG conforms well to the Kozak consensus sequence for an initiator methionine, and that the N-terminal amino acid of MPF, Leu, which is followed by Ala, Gly, Gln, and Thr(4Yamaguchi N. Hattori K. Oh-eda M. Kojima T. Imai N. Ochi N. J. Biol. Chem. 1994; 269: 805-808Abstract Full Text PDF PubMed Google Scholar), was located at nucleotides 191-193. This cDNA encodes a 622-amino acid long precursor, whose N-terminal 33 hydrophobic amino acids correspond to a peptide signal sequence. The remaining portion of this precursor has a deduced molecular mass of 66.8 kDa, which is different from the molecular size of natural MPF, i.e. 32 kDa. However, when an in vitro translation reaction was performed on RNA templates, transcribed in vitro from a vector harboring MPF cDNA downstream of the T7 promoter, the molecular weight of the in vitro translation product was equivalent to that predicted from the nucleotide sequence of the MPF cDNA (data not shown). A dibasic proteolytic cleavage site RXRXRR and four potential N-glycosylation sites were found in the MPF precursor amino acid sequence. No significant homology to any sequences in GenBank and EMBL was revealed by comparison of nucleotide and predicted amino acid sequences.Figure 2:cDNA structure and deduced amino acid sequence of MPF precursor. The nucleotide sequence of pKPO27 cDNA and the deduced amino acid sequence are shown. The numbering of nucleotides in the cDNA is indicated at the end of each line. The predicted amino acid sequence of pre-proMPF is numbered by designating the first methionine as 1. The four potential N-linked glycosylation sites (Asn-X-Ser/Thr, X, any amino acid except for Pro) are indicated by N-CHO. A potential polyadenylation signal is dot underlined in the 3′-untranslated region. The bold underlined Arg-X-Arg-X-Arg-Arg precedes the potential proteolytic cleavage site.View Large Image Figure ViewerDownload Hi-res image Download (PPT)COS Cell Expression of MPF cDNATo further verify the identity of the MPF cDNA, an expression plasmid pRVHKPO27f was constructed and transfected into COS-7 cells, and the culture supernatant was subjected to megakaryocyte colony-forming assay. The assay was performed in the presence of anti-mouse IL-6 receptor antibody, since the culture supernatant of COS cells contains IL-6. The culture supernatant of cDNA-transfected COS cells, but not that of cells transfected with the vector alone, potentiated megakaryocyte-colony formation. Western blotting analysis was performed on the aforementioned supernatants using an antiserum raised against rMPF expressed in E. coli. In the case of cDNA-transfected cells, a band corresponding to MPF protein was detected at approximately 33 kDa as shown in Fig. 3. Since the 55-kDa band, detected in both cases, is also present in FCS, it was presumably not related to rMPF (data not shown).Figure 3:Detection of MPF in a culture supernatant of transfected COS cells. The culture supernatant of cDNA-transfected COS cells was concentrated by Centriprep-10 (Amicon), electrophoresed on a 12% gel (120 V, 2 h), and transferred on a nitrocellulose membrane. MPF was detected with rabbit anti-MPF antiplasma and alkaline phosphatase-conjugated antibody to rabbit IgG (Cappel). Lane 1, culture supernatant of mock transfected COS cells; lane 2, cDNA transfected COS cells.View Large Image Figure ViewerDownload Hi-res image Download (PPT)CHO Cell Expression of MPF cDNAAfter transfection of pEFDKPO27f and establishment of FKL5F stable transformants resistant to 10 nM methotrexate, whose culture medium exhibited the highest concentration of MPF (5 mg/liter) were selected. The molecular species of the MPF protein produced in these cells were examined by Western blotting, and two bands of different molecular size, 33 and 30 kDa, were detected in the culture supernatant. In contrast, HPC-Y5 cells and cDNA-transfected COS cells expressed only the 33-kDa form.Purification and Characterization of rMPF Produced in CHO CellsEach of the two purified forms appeared as a single band under both nonreducing and reducing SDS-PAGE conditions (Fig. 4). To clarify the difference in their molecular weight, their N- and C-terminal amino acid sequences were analyzed. Both forms had the same N-terminal amino acids, i.e. Ser1, Leu4, and Gly6.Figure 4:SDS-PAGE analysis of the purified recombinant MPF. The two MPF forms (100 ng) were electrophoresed on a 12% gel (120 V, 2 h) and stained with Coomassie Brilliant Blue R-250. Apparent molecular weight was determined by using a molecular weight standard mixture (Bio-Rad). Lane 1, 33-kDa MPF; lane 2, 30-kDa MPF.View Large Image Figure ViewerDownload Hi-res image Download (PPT)The C-terminal sequences were identified by analyzing the C-terminal fragments obtained from the 33- and 30-kDa MPF after cyanogen bromide cleavage and endoproteinase Asp-N digestion. The amino acid sequence of the C-terminal peptide derived from the 30-kDa MPF was determined as Met-Asp-Ala-Leu-Arg-Gly-Leu-Leu-Pro-Val-Leu-Gly-Gln-Pro-Ile-Ile-Arg261.The C-terminal peptide obtained from the 33-kDa MPF by cyanogen bromide cleavage was further digested with endoproteinase Asp-N, since this peptide was too long to determine the complete amino acid sequence. The peaks obtained by reverse phase HPLC were analyzed in a protein sequencer, and their amino acid sequences, Met-Asp-Ala-Leu-Arg-Gly-Leu-Leu-ProVal-Leu-Gly-Gln-Pro-Ile-Ile-Arg-Ser-Ile-Pro-Gln-Gly-Ile-ValAla-Ala-Trp-Arg-Gln-Arg-Ser-Ser-Arg277 and Asp-Pro-Ser-Trp-Arg-Gln-Pro-Glu-Arg286 were identified. These results demonstrated that the 30-kDa rMPF was generated by truncation of the C-terminal 25 amino acid residues from the 33-kDa rMPF.Activity of Recombinant MPFsThe Meg-POT activity of the rMPFs was determined by megakaryocyte colony-forming assay, in comparison with native MPF derived from HPC-Y5 as a positive control. The 33-kDa rMPF potentiated megakaryocyte-colony formation in the presence of mouse IL-3 in a dose dependent manner, as did native MPF (Fig. 5). On the other hand, as shown in Fig. 6, the 30-kDa rMPF showed no Meg-POT activity in the dose range of 0.156 to 40 ng/ml.Figure 5:Megakaryocyte potentiating activities of natural and recombinant MPFs. Bone marrow cells (2 × 105) were cultured as described under "Materials and Methods." Megakaryocyte colonies were scored using dehydrated cultures stained for acetylcholine esterase. Each point represents the mean of duplicate cultures. Similar results were obtained with repeated experiments, and a typical pattern is shown here. ○, natural MPF; •, 33-kDa rMPF; ▵, rhIL-6; ■, mouse IL-3 alone.View Large Image Figure ViewerDownload Hi-res image Download (PPT)Figure 6:Megakaryocyte potentiating activities of 30- and 33-kDa rMPFs. The Meg-POT activities of two molecular species of MPF were determined as described under "Materials and Methods." Each value represents the mean of duplicate cultures. Similar results were obtained with repeated experiments, and a typical pattern is shown here.View Large Image Figure ViewerDownload Hi-res image Download (PPT)Using a sandwich enzyme-linked immunosorbent assay, as shown in Fig. 7, the antigenicity of 33-kDa rMPF was detected with the prepared anti-MPF monoclonal and polyclonal antibodies, whereas the 30-kDa rMPF displayed only a weak antigenicity, approximately 1/50 of 33-kDa rMPF, for any antibody. Thus, deletion of the C-terminal 25 amino acids from the 33-kDa rMPF decreased the antigenicity of the protein for these antibodies.Figure 7:Immunological activities of 30- and 33-kDa rMPFs. Two molecular species of MPF samples were incubated in a 96-well plate coated with mouse anti-MPF monoclonal antibody against MPF. The detection was then carried out with rabbit anti-MPF antiplasma and anti-rabbit IgG-horseradish peroxidase-conjugated antibody, and absorbance was read at 490 nm.View Large Image Figure ViewerDownload Hi-res image Download (PPT)MPF mRNA Expression in TissuesTo obtain further insight into MPF function, the expression of MPF mRNA was examined by Northern blot analysis using labeled MPF cDNA as a probe. MPF mRNA was detected in HPC-Y5 cells, with an approximate molecular size of 2.4 kilobases and a low expression level, which was in agreement with the low content of MPF in the culture supernatant of HPC-Y5 cells. We also examined the expression of the MPF gene in various human tissues, and the 2.4-kilobase band was detected only in lung. With a long exposure, MPF mRNA could be detected in heart, placenta, and kidney in lower level than in lung, but not in any other tissues so far examined, i.e. brain, liver, skeletal muscle, or pancreas (Fig. 8).Figure 8:MPF mRNA distribution in human tissues. A, poly(A)+ RNA (2 μg) prepared from HPC-Y5 was size-fractionated on formaldehyde agarose gels (1%), and transferred to Hybond-N+. B, lane 1, heart; lane 2, brain; lane 3, placenta; lane 4, lung; lane 5, liver; lane 6, skeletal muscle; lane 7, kidney; lane 8, pancreas.View Large Image Figure ViewerDownload Hi-res image Download (PPT)DISCUSSIONWe have isolated a cDNA for hMPF, which exhibits a Meg-POT activity in the presence of murine IL-3 in a colony-forming assay with mouse bone marrow cells, by means of PCR and plaque hybridization methods. By structural analysis of the cDNA, the primary translation product of MPF was shown to consist of 622 amino acid residues. The sequence of the mature MPF protein (33 kDa) starts at Ser34 and ends at Arg286 in complete agreement with that of natural MPF(4Yamaguchi N. Hattori K. Oh-eda M. Kojima T. Imai N. Ochi N. J. Biol. Chem. 1994; 269: 805-808Abstract Full Text PDF PubMed Google Scholar), and the C-terminal Arg residue of the mature 33-kDa MPF is followed by a 336-amino acid polypeptide. Several polypeptide hormones are synthesized as large precursor proteins, such as human pro-parathyroid hormone related protein(12Suva I.J. Winslow G.A. Wettenhall R.E.H. Hammonds R.G. Moseley J.M. Diefenbach-Jagger H. Rodda C.P. Kemp B.E. Rodriguez H. Chen E.Y. Hudson P.J. Martin T.J. Wood W.I. Science. 1987; 237: 893-896Crossref PubMed Scopus (1149) Google Scholar), porcine proendothelin-1(13Yanagisawa M. Kurihara H. Kimura S. Tomobe Y. Kobayashi M. Mitsui Y. Yazaki Y. Goto K. Masaki T. Nature. 1988; 332: 411-415Crossref PubMed Scopus (10186) Google Scholar), human pro-transforming growth factor β1(14Derynck R. Jarret J.A. Chen E.Y. Eaton D.H. Bell J.R. Assoian R.K. Roberts A.B. Sporn M.B. Goeddel D.V. Nature. 1985; 316: 701-704Crossref PubMed Scopus (1366) Google Scholar), mouse pro-nerve growth factor(15Scott J. Selby M. Urdea M. Quiroga M. Bell G.I. Rutter W.J. Nature. 1983; 302: 538-540Crossref PubMed Scopus (345) Google Scholar), and human pro-platelet-derived growth factor(16Betsholtz C. Johnsson A. Heldin C. Westermark B. Lind P. Urdea M.S. Eddy R. Shows T.B. Philpott K. Mellor A.L. Knott T.J. Scott J. Nature. 1986; 320: 695-699Crossref PubMed Scopus (537) Google Scholar). In each of these cases, active polypeptide sequences are usually bonded by pairs of basic amino acid residues such as Arg-Arg or Lys-Arg, and it is at these sites that proteolytic processing occurs. Watanabe et al.(17Watanabe T. Nakagawa T. Ikemizu J. Nagahama M. Murakami K. Nakayama K. J. Biol. Chem. 1992; 267: 8270-8274Abstract Full Text PDF PubMed Google Scholar, 18Watanabe T. Murakami K. Nakayama K. FEBS Lett. 1993; 320: 215-218Crossref PubMed Scopus (56) Google Scholar) have demonstrated that the sequence Arg-X-Arg/Lys-X-Lys/Arg-Arg is a signal for precursor cleavage catalyzed with furin, a mammalian homologue of the yeast precursor-processing endoprotease Kex2, within the constitutive secretory pathway in nonendocrine cells. The sequence Arg290-Pro-Arg-Phe-Arg-Arg295 deduced from the MPF cDNA matches this cleavage signal model. The C-terminal Arg residues of the 33- and 30-kDa rMPFs, Arg286, and Arg261, are located 9 and 34 amino acid residues upstream of this cleavage signal, respectively. Moreover, the hydrophobicity profile predicts that the signal is located in a hydrophilic region between Trp271 and Glu310. This suggests that the MPF precursor would fold and then, be successively processed with furin-like and trypsin-like proteases. A similar processing has been found in leukocyte-derived natural interferon-α (19Levy W.P. Rubinstein M. Shively J. DelValle U. Lai C.-Y. Moschera J. Brink L. Gerber L. Stein S. Pestka S. Proc. Natl. Acad. Sci. U. S. A. 1981; 78: 6186-6190Crossref PubMed Scopus (88) Google Scholar) and interferon-γ(20Pan Y.C. Stern A.S. Familletti P.C. Khan F.R. Chizzonite R. Eur. J. Biochem. 1987; 166: 145-149Crossref PubMed Scopus (30) Google Scholar, 21Rinderknecht E. O'Connor B. Redriguez H. J. Biol. Chem. 1984; 259: 6790-6797Abstract Full Text PDF PubMed Google Scholar). Although cleavage of the precursor gives rise to the mature MPF, it is not known if other peptides released from the C-terminal region of the MPF precursor are also biologically active.The 33-kDa rMPF displayed a Meg-POT activity, whereas the 30-kDa rMPF, which was generated by truncation of the C-terminal 25 amino acid residues from the 33-kDa rMPF, possessed no Meg-POT activity equivalent to that of natural hMPF and IL-6. Furthermore, the 30-kDa rMPF was not antigenic for any of the antibodies raised against the rMPF precursor protein produced in E. coli, although the 30- and 33-kDa forms of rMPF are detectable in Western blotting analysis with these antibodies. Therefore, the C-terminal 25 amino acid residues are not epitopes. Circular dichroism (CD) analysis showed no influence of C-terminal truncation on the secondary structure, that is, there are no significant differences between the CD spectra of the 33- and 30-kDa rMPFs. 2M. Oh-eda, K. Hattori, and T. Kojima, unpublished data. However, Hattori et al. (22Hattori M. Ametani A. Katakura Y. Shimizu M. Kaminogawa S. J. Biol. Chem. 1993; 268: 22414-22419Abstract Full Text PDF PubMed Google Scholar) have previously shown that monoclonal antibodies can detect subtle conformational changes in local areas within a protein molecule during denaturation, by determining affinity changes. Shortle and Meeker (23Shortle D. Meeker A.K. Biochemistry. 1989; 28: 936-944Crossref PubMed Scopus (273) Google Scholar) have also found that removal of the C-terminal 13 amino acids of staphylococcal nuclease is sufficient to destabilize the protein native state or stabilize it in the denatured state. Therefore, loss of the C-terminal 25 amino acids might give rise to a local conformational change, altering the antigenicity of MPF.Slodowski et al. (24Slodowski O. Bohm J. Schone B. Otto B. Eur. J. Biochem. 1991; 202: 1133-1140Crossref PubMed Scopus (31) Google Scholar) have previously examined the biological function of the C-terminal 20 amino acid residues of IFN-γ. The antiviral activities of the INF-γ analogue proteins lacking 14 (C-14) or more amino acids from the C-terminal are less than 2% of the native protein activity. In contrast, a variant, shortened by 11 only amino acids (C-11), showed a higher biological activity than the wild type INF-γ. CD analysis showed no influence of these C-terminal truncations on the secondary structure. In the case of 33-kDa MPF, however, removal of the Arg262-Arg286 region leads to a drastic loss in biological activity and antigenicity, while truncation at Arg286, excising the 33-kDa rMPF from its precursor, may result in a significant increase in activity. The loss of biological activity of the 33-kDa rMPF due to the absence of its C-terminal peptide may be linked to the delicate regulation of megakaryocytopoiesis in vivo. It remains to be determined whether MPF exists in vivo as a precursor of the shorter species, 33- and 30-kDa MPF.MPF was originally isolated from a pancreatic cancer cell line, HPC-Y5, however, Northern blot analysis shows that the MPF gene is expressed in the lung, not in the pancreas. Since the structure of the lung consist of aloveoli and abundant capillaries, and is fraught with the danger of bleeding, this would suggest that MPF might play a role in the growth of megakaryocytes and/or the regulation of platelet production. But since MPF is weakly expressed in heart, placenta, and kidney, MPF may exhibit other biological activities. INTRODUCTIONMegakaryocytes originate from pluripotent hematopoietic stem cells through a complex process involving commitment of the pluripotent hematopoietic progenitor to megakaryocytic precursor cells and their mitotic amplification. The regulatory system governing megakaryocytopoiesis and platelet production is thought to take place in at least two stages, 1) during proliferation and differentiation of megakaryocytic progenitor cells, leading to the production of megakaryocytes, and 2) during maturation of megakaryocytes which leads to the production of platelets. Megakaryocyte proliferation is thought to be dependent on an essential megakaryocyte colony-stimulating factor, and this proliferation can be potentiated in vitro by ancillary megakaryocyte potentiators (Meg-POT) 1The abbreviations used are: Meg-POTmegakaryocyte potentiatorMPFmegakaryocyte potentiating factorPCRpolymerase chain reactionhhumanCHOChinese hamster ovaryFCSfetal calf serumHPLChigh performance liquid chromatographyPAGEpolyacrylamide gel electrophoresisILinterleukin. (1Williams N. Eger R.R. Jackson H.M. Nelson D.J. J. Cell. Physiol. 1982; 110: 101-104Crossref PubMed Scopus (117) Google Scholar, 2Gordon M.S. Hoffman R. Blood. 1992; 80: 302-307Crossref PubMed Google Scholar, 3Williams N. Jackson H. Ralph P. Nakoinz I. Blood. 1981; 57: 157-163Crossref PubMed Google Scholar), which also stimulate the maturation of the megakaryocytes. We have recently identified, in the culture supernatant of the human pancreatic cancer cells HPC-Y5, a novel megakaryocyte potentiating factor (hMPF), which stimulates the megakaryocyte colony forming activity of murine interleukin-3 in mouse bone marrow cell culture(4Yamaguchi N. Hattori K. Oh-eda M. Kojima T. Imai N. Ochi N. J. Biol. Chem. 1994; 269: 805-808Abstract Full Text PDF PubMed Google Scholar). The factor was found to consist of a single polypeptide of about 32 kDa with at least one N-linked sugar chain. In this paper, we describe the molecular cloning and characterization of the cDNA encoding human MPF.