Plant molecular farming-derived epidermal growth factor revolutionizes hydrogels for improving glandular epithelial organoid biofabrication
dc.contributor.author | Phan T.V. | |
dc.contributor.author | Oo Y. | |
dc.contributor.author | Rodboon T. | |
dc.contributor.author | Nguyen T.T. | |
dc.contributor.author | Sariya L. | |
dc.contributor.author | Chaisuparat R. | |
dc.contributor.author | Phoolcharoen W. | |
dc.contributor.author | Yodmuang S. | |
dc.contributor.author | Ferreira J.N. | |
dc.contributor.other | Mahidol University | |
dc.date.accessioned | 2023-09-02T18:01:47Z | |
dc.date.available | 2023-09-02T18:01:47Z | |
dc.date.issued | 2023-08-01 | |
dc.description.abstract | Epidermal growth factor (EGF) is a known signaling cue essential towards the development and organoid biofabrication particularly for exocrine glands. This study developed an in vitro EGF delivery platform with Nicotiana benthamiana plant-produced EGF (P-EGF) encapsulated on hyaluronic acid/alginate (HA/Alg) hydrogel to improve the effectiveness of glandular organoid biofabrication in short-term culture systems. Primary submandibular gland epithelial cells were treated with 5 - 20 ng/mL of P-EGF and commercially available bacteria-derived EGF (B-EGF). Cell proliferation and metabolic activity were measured by MTT and luciferase-based ATP assays. P-EGF and B-EGF 5 - 20 ng/mL promoted glandular epithelial cell proliferation during 6 culture days on a comparable fashion. Organoid forming efficiency and cellular viability, ATP-dependent activity and expansion were evaluated using two EGF delivery systems, HA/Alg-based encapsulation and media supplementation. Phosphate buffered saline (PBS) was used as a control vehicle. Epithelial organoids fabricated from PBS-, B-EGF-, and P-EGF-encapsulated hydrogels were characterized genotypically, phenotypically and by functional assays. P-EGF-encapsulated hydrogel enhanced organoid formation efficiency and cellular viability and metabolism relative to P-EGF supplementation. At culture day 3, epithelial organoids developed from P-EGF-encapsulated HA/Alg platform contained functional cell clusters expressing specific glandular epithelial markers such as exocrine pro-acinar (AQP5, NKCC1, CHRM1, CHRM3, Mist1), ductal (K18, Krt19), and myoepithelial (α-SMA, Acta2), and possessed a high mitotic activity (38-62% Ki67 cells) with a large epithelial progenitor population (∼70% K14 cells). The P-EGF encapsulation strikingly upregulated the expression of pro-acinar AQP5 cells through culture time when compared to others (B-EGF, PBS). Thus, the utilization of Nicotiana benthamiana in molecular farming can produce EGF biologicals amenable to encapsulation in HA/Alg-based in vitro platforms, which can effectively and promptly induce the biofabrication of exocrine gland organoids. | |
dc.identifier.citation | SLAS technology Vol.28 No.4 (2023) , 278-291 | |
dc.identifier.doi | 10.1016/j.slast.2023.03.002 | |
dc.identifier.eissn | 24726311 | |
dc.identifier.pmid | 36966988 | |
dc.identifier.scopus | 2-s2.0-85167842355 | |
dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/20.500.14594/89142 | |
dc.rights.holder | SCOPUS | |
dc.subject | Medicine | |
dc.title | Plant molecular farming-derived epidermal growth factor revolutionizes hydrogels for improving glandular epithelial organoid biofabrication | |
dc.type | Article | |
mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85167842355&origin=inward | |
oaire.citation.endPage | 291 | |
oaire.citation.issue | 4 | |
oaire.citation.startPage | 278 | |
oaire.citation.title | SLAS technology | |
oaire.citation.volume | 28 | |
oairecerif.author.affiliation | Chulalongkorn University | |
oairecerif.author.affiliation | Mahidol University | |
oairecerif.author.affiliation | Faculty of Medicine, Chulalongkorn University |