Encapsulation of Primary Salivary Gland Acinar Cell Clusters and Intercalated Ducts (AIDUCs) within Matrix Metalloproteinase (MMP)-Degradable Hydrogels to Maintain Tissue Structure and Function.
Encapsulation of Primary Salivary Gland Acinar Cell Clusters and Intercalated Ducts (AIDUCs) within Matrix Metalloproteinase (MMP)-Degradable Hydrogels to Maintain Tissue Structure and Function.
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DOI:
10.1002/adhm.202101948
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发表时间:
2022-04
影响因子:
10
通讯作者:
Benoit DSW
中科院分区:
文献类型:
--
作者:
Song Y;Sharipol A;Uchida H;Ingalls MH;Piraino L;Mereness JA;Moyston T;DeLouise LA;Ovitt CE;Benoit DSW
Progress in the development of salivary gland regenerative strategies is limited by poor maintenance of the secretory function of salivary gland cells (SGCs) in vitro. To reduce the precipitous loss of secretory function, a modified approach to isolate intact acinar cell clusters and intercalated ducts (AIDUCs), rather than commonly used single cell suspension, was investigated. This isolation approach yielded AIDUCs that maintain many of the cell-cell and cell-matrix interactions of intact glands. Encapsulation of AIDUCs in matrix metalloproteinase (MMP)-degradable PEG hydrogels promoted self-assembly into salivary gland mimetics (SGm) with acinar-like structure. Expression of Mist1, a transcription factor associated with secretory function, was detectable throughout the in vitro culture period up to 14 days. Immunohistochemistry also confirmed expression of acinar cell markers (NKCC1, PIP and AQP5), duct cell markers (K7 and K5), and myoepithelial cell markers (SMA). Robust carbachol and ATP-stimulated calcium flux was observed within the SGm for up to 14 days after encapsulation, indicating that secretory function is maintained. Though some acinar-to-ductal metaplasia was observed within SGm, it was reduced compared to previous reports. In conclusion, cell-cell interactions maintained within AIDUCs together with the hydrogel microenvironment may be a promising platform for salivary gland regenerative strategies.
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影响因子:
3
作者:
Varghese JJ;Hansen ME;Sharipol A;Ingalls MH;Ormanoski MA;Newlands SD;Ovitt CE;Benoit DSW
通讯作者:
Benoit DSW
影响因子:
3.7
作者:
An H;Kim JY;Oh E;Lee N;Cho Y;Seo JH
通讯作者:
Seo JH
影响因子:
9.7
作者:
Hoffman, Michael D.;Van Hove, Amy H.;Benoit, Danielle S. W.
通讯作者:
Benoit, Danielle S. W.
影响因子:
2.8
作者:
CASELITZ, J;SCHMITT, P;SCHUPPAN, D
通讯作者:
SCHUPPAN, D
DOI:
10.1097/01.wcb.0000141558.40491.75
发表时间:
2004-12-01
影响因子:
6.3
作者:
Hedtjarn, M;Mallard, C;Hagberg, H
通讯作者:
Hagberg, H