4.6 Article

Identification and Functional Analysis of the Cell Proliferation Regulator, Insulin-like Growth Factor 1 (IGF1) in Freshwater Pearl Mussel (Hyriopsis cumingii)

期刊

BIOLOGY-BASEL
卷 11, 期 9, 页码 -

出版社

MDPI
DOI: 10.3390/biology11091369

关键词

Hyriopsis cumingii; HcIGF1; RNA interference; proliferation activity

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资金

  1. National Key R&D Program of China [2018YFD0901406]
  2. National Natural Science Foundation of China [31872565]
  3. Program of the Shanghai Academic Research Leader [19XD1421500]

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In this study, the function of IGF1 in Hyriopsis cumingii was explored. It was found that IGF1 plays a role in promoting cell proliferation through the PI3K/AKT signaling pathway. The results provide a new method to solve the low proliferative capacity of mantle cells in vitro and contribute to a better understanding of the growth regulation mechanism of H. cumingii.
Simple Summary Hyriopsis cumingii (H. cumingii, mussels) is an important freshwater pearl shellfish species, and its mantle is the most important tissue during shell and pearl mineralization. However, the low proliferative capacity of mantle cells during in vitro culture hinders the establishment of stable cell lines. In this study, we identified and explored the function of IGF1. The results show that IGF1 has a typical IIGF structural domain, exerts biological functions through the PI3K/AKT signaling pathway, and that the recombinant protein significantly promotes the proliferation of mantle cells. Our findings will help to further extend the culture time of mantle cells as well as to understand the growth regulation mechanism of mussels. Insulin-like growth factor 1 (IGF1) plays an important regulatory role in the regulation of growth, differentiation, and anabolism in a variety of cells. In this study, the full-length cDNA of the IGF1 gene was cloned from Hyriopsis cumingii, named HcIGF1. The expression level of HcIGF1 in six tissues (adductor muscle, foot, hepatopancreas, gill, mantle, and gonad) was determined. In addition, the localization of HcIGF1 in the mantle was analyzed by in situ hybridization, and finally the function of HcIGF1 was explored by RNA interference and prokaryotic expression. The results showed that the amino acid sequence contained a typical IIGF structural domain. The phylogenetic tree showed that HcIGF1 clustered with other marine bivalve sequences. Quantitative real-time PCR and in situ hybridization analysis showed that HcIGF1 was expressed in all tissues. The highest expression was in the foot and the lowest was in the mantle. In the mantle tissue, the hybridization signal was mainly concentrated in the outer mantle. After RNA interference, the expression of IGF1 was found to be significantly decreased (p < 0.05), and its related genes IGF1R, AKT1, and cyclin D2 were downregulated, while MAPK1 were upregulated. The recombinant HcIGF1 protein was purified and its growth-promoting effect was investigated. The results showed that the recombinant HcIGF1 protein could significantly promote the proliferative activity of the mantle cells of mussels, with the best proliferative effect at 12.5 mu g/mL. The results of this study provide a new method to solve the problem of weak proliferation of shellfish cells in vitro and lay the foundation for further understanding of the growth regulation mechanism of H. cumingii, as well as a better understanding of the physiological function of IGF1 in mollusks.

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