DOI QR코드

DOI QR Code

Adipogenic function of tetranectin mediated by enhancing mitotic clonal expansion via ERK signaling

  • Go, Seulgi (Department of Medical Biotechnology and Research Institute of Cell Culture, Yeungnam University) ;
  • Park, Jihyun (Department of Medical Biotechnology and Research Institute of Cell Culture, Yeungnam University) ;
  • Rahman, Safikur (Department of Botany, Munshi Singh College, BR Ambedkar Bihar University) ;
  • Jin, Juno (Department of Medical Biotechnology and Research Institute of Cell Culture, Yeungnam University) ;
  • Choi, Inho (Department of Medical Biotechnology and Research Institute of Cell Culture, Yeungnam University) ;
  • Kim, Jihoe (Department of Medical Biotechnology and Research Institute of Cell Culture, Yeungnam University)
  • 투고 : 2021.02.16
  • 심사 : 2021.03.06
  • 발행 : 2021.07.31

초록

Tetranectin (TN), an adipogenic serum protein, enhances adipocyte differentiation, however, its functional mechanism has yet to be elucidated. In the present study, we investigated the adipogenic function of TN by using medium containing TN-depleted fetal bovine serum (TN-del-FBS) and recombinant mouse TN (mTN). The adipocyte differentiation of 3T3-L1 cells was significantly enhanced by mTN supplementation essentially at differentiation induction, which indicated a potential role of the protein in the early differentiation phase. The adipogenic effect of mTN was more significant with insulin in the differentiation induction cocktail, implicating their close functional relationship. mTN enhanced not only the proliferation of growing cells, but also mitotic clonal expansion (MCE) that is a prerequisite for adipocyte differentiation in the early phase. Consistently, mTN increased the phosphorylation of ERK in the early phase of adipocyte differentiation. Results of this study demonstrate that the adipogenic function of mTN is mediated by enhancing MCE via ERK signaling.

키워드

과제정보

This research was supported by Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education (2020R1A6A1A03044512) and Yeungnam University research grants in 2020.

참고문헌

  1. Clemmensen I, Petersen LC and Kluft C (1986) Purification and characterization of a novel, oligomeric, plasminogen kringle 4 binding protein from human plasma: tetranectin. Eur J Biochem 156, 327-333 https://doi.org/10.1111/j.1432-1033.1986.tb09586.x
  2. Westergaard UB, Andersen MH, Heegaard CW, Fedosov SN and Petersen TE (2003) Tetranectin binds hepatocyte growth factor and tissue-type plasminogen activator. Eur J Biochem 270, 1850-1854 https://doi.org/10.1046/j.1432-1033.2003.03549.x
  3. Tuxen MK, Soletormos G and Dombernowsky P (1995) Tumor markers in the management of patients with ovarian cancer. Cancer Treat Rev 21, 215-245 https://doi.org/10.1016/0305-7372(95)90002-0
  4. Hogdall CK, Christensen L and Clemmensen I (1994) [Tetranectin, a plasma and tissue protein--a prognostic marker of breast and ovarian cancer]. Ugeskr Laeger 156, 6190-6195
  5. Wewer UM and Albrechtsen R (1992) Tetranectin, a plasminogen kringle 4-binding protein. Cloning and gene expression pattern in human colon cancer. Lab Invest 67, 253-262
  6. Nielsen H, Clemmensen I, Nielsen HJ and Drivsholm A (1990) Decreased tetranectin in multiple myeloma. Am J Hematol 33, 142-144 https://doi.org/10.1002/ajh.2830330213
  7. Christensen L and Clemmensen I (1991) Differences in tetranectin immunoreactivity between benign and malignant breast tissue. Histochemistry 95, 427-433 https://doi.org/10.1007/BF00315737
  8. Hogdall CK, Christensen L and Clemmensen I (1993) The prognostic value of tetranectin immunoreactivity and plasma tetranectin in patients with ovarian cancer. Cancer 72, 2415-2422 https://doi.org/10.1002/1097-0142(19931015)72:8<2415::AID-CNCR2820720820>3.0.CO;2-N
  9. Zhu HF, Zhang XH, Gu CS et al (2019) Cancer-associated fibroblasts promote colorectal cancer progression by secreting CLEC3B. Cancer Biol Ther 20, 967-978 https://doi.org/10.1080/15384047.2019.1591122
  10. Wewer UM, Iba K, Durkin ME et al (1998) Tetranectin is a novel marker for myogenesis during embryonic development, muscle regeneration, and muscle cell differentiation in vitro. Dev Biol 200, 247-259 https://doi.org/10.1006/dbio.1998.8962
  11. Wewer UM, Ibaraki K, Schjorring P, Durkin ME, Young MF and Albrechtsen R (1994) A potential role for tetranectin in mineralization during osteogenesis. J Cell Biol 127, 1767-1775 https://doi.org/10.1083/jcb.127.6.1767
  12. Park J, Park J, Nahm SS, Choi I and Kim J (2013) Identification of anti-adipogenic proteins in adult bovine serum suppressing 3T3-L1 preadipocyte differentiation. BMB Rep 46, 582-587 https://doi.org/10.5483/BMBRep.2013.46.12.082
  13. Armani A, Mammi C, Marzolla V et al (2010) Cellular models for understanding adipogenesis, adipose dysfunction, and obesity. J Cell Biochem 110, 564-572 https://doi.org/10.1002/jcb.22598
  14. Bost F, Aouadi M, Caron L and Binetruy B (2005) The role of MAPKs in adipocyte differentiation and obesity. Biochimie 87, 51-56 https://doi.org/10.1016/j.biochi.2004.10.018
  15. Tang QQ, Otto TC and Lane MD (2003) Mitotic clonal expansion: a synchronous process required for adipogenesis. Proc Natl Acad Sci U S A 100, 44-49 https://doi.org/10.1073/pnas.0137044100
  16. Sale EM, Atkinson PG and Sale GJ (1995) Requirement of MAP kinase for differentiation of fibroblasts to adipocytes, for insulin activation of p90 S6 kinase and for insulin or serum stimulation of DNA synthesis. EMBO J 14, 674-684 https://doi.org/10.1002/j.1460-2075.1995.tb07046.x
  17. Fuhlendorff J, Clemmensen I and Magnusson S (1987) Primary structure of tetranectin, a plasminogen kringle 4 binding plasma protein: homology with asialoglycoprotein receptors and cartilage proteoglycan core protein. Biochemistry 26, 6757-6764 https://doi.org/10.1021/bi00395a027
  18. Park J, Park J, Jeong J, Cho KH, Choi I and Kim J (2015) Identification of tetranectin as adipogenic serum protein. Biochem Biophys Res Commun 460, 583-588 https://doi.org/10.1016/j.bbrc.2015.03.073
  19. Park J, Ryu DY, Rahman S and Kim J (2019) Adipogenic function of mouse tetranectin and identification of its functional domain. Biochem Biophys Res Commun 519, 645-651 https://doi.org/10.1016/j.bbrc.2019.09.052
  20. Schmidt W, Poll-Jordan G and Loffler G (1990) Adipose conversion of 3T3-L1 cells in a serum-free culture system depends on epidermal growth factor, insulin-like growth factor I, corticosterone, and cyclic AMP. J Biol Chem 265, 15489-15495 https://doi.org/10.1016/S0021-9258(18)55422-3
  21. Kuri-Harcuch W and Green H (1978) Adipose conversion of 3T3 cells depends on a serum factor. Proc Natl Acad Sci U S A 75, 6107-6109 https://doi.org/10.1073/pnas.75.12.6107
  22. Liu J, Liu Z, Liu Q et al (2018) CLEC3B is downregulated and inhibits proliferation in clear cell renal cell carcinoma. Oncol Rep 40, 2023-2035
  23. Prusty D, Park BH, Davis KE and Farmer SR (2002) Activation of MEK/ERK signaling promotes adipogenesis by enhancing peroxisome proliferator-activated receptor gamma (PPARgamma) and C/EBPalpha gene expression during the differentiation of 3T3-L1 preadipocytes. J Biol Chem 277, 46226-46232 https://doi.org/10.1074/jbc.M207776200
  24. Park J, Nahm SS, Choi I and Kim J (2013) Identification of anti-adipogenic proteins in adult bovine serum suppressing 3T3-L1 preadipocyte differentiation. BMB Rep 46, 582-587 https://doi.org/10.5483/BMBRep.2013.46.12.082
  25. Park J, Jeong J, Cho KH, Choi I and Kim J (2015) Identification of tetranectin as adipogenic serum protein. Biochem Biophys Res Commun 460, 583-588 https://doi.org/10.1016/j.bbrc.2015.03.073
  26. Hossain M, Imran KM, Rahman MS, Yoon D, Marimuthu V and Kim YS (2020) Sinapic acid induces the expression of thermogenic signature genes and lipolysis through activation of PKA/CREB signaling in brown adipocytes. BMB Rep 53, 142-147 https://doi.org/10.5483/BMBRep.2020.53.3.093