Cited by 9Pancreatic function and diabetesPluripotent Stem Cells ResearchDevelopmental Biology and Gene Regulation

Colony-Forming Progenitor Cells in the Postnatal Mouse Liver and Pancreas Give Rise to Morphologically Distinct Insulin-Expressing Colonies in 3D Cultures

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Jin, Liang, Feng, Tao, Chai, Jing, Ghazalli, Nadiah, Gao, Dan, Zerda, Ricardo, Li, Zhuo, Hsu, Jasper +4 more·2014·The Review of Diabetic Studies

Abstract

In our previous studies, colony-forming progenitor cells isolated from murine embryonic stem cell-derived cultures were differentiated into morphologically distinct insulin-expressing colonies. These colonies were small and not light-reflective when observed by phase-contrast microscopy (therefore termed "Dark" colonies). A single progenitor cell capable of giving rise to a Dark colony was termed a Dark colony-forming unit (CFU-Dark). The goal of the current study was to test whether endogenous pancreas, and its developmentally related liver, harbored CFU-Dark. Here we show that dissociated single cells from liver and pancreas of one-week-old mice give rise to Dark colonies in methylcellulose-based semisolid culture media containing either Matrigel or laminin hydrogel (an artificial extracellular matrix protein). CFU-Dark comprise approximately 0.1% and 0.03% of the postnatal hepatic and pancreatic cells, respectively. Adult liver also contains CFU-Dark, but at a much lower frequency (~0.003%). Microfluidic qRT-PCR, immunostaining, and electron microscopy analyses of individually handpicked colonies reveal the expression of insulin in many, but not all, Dark colonies. Most pancreatic insulin-positive Dark colonies also express glucagon, whereas liver colonies do not. Liver CFU-Dark require Matrigel, but not laminin hydrogel, to become insulin-positive. In contrast, laminin hydrogel is sufficient to support the development of pancreatic Dark colonies that express insulin. Postnatal liver CFU-Dark display a cell surface marker CD133⁺CD49f(low)CD107b(low) phenotype, while pancreatic CFU-Dark are CD133⁻. Together, these results demonstrate that specific progenitor cells in the postnatal liver and pancreas are capable of developing into insulin-expressing colonies, but they differ in frequency, marker expression, and matrix protein requirements for growth.

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  • Using aECM-lam, other morphologically-distinct organoids were formed from murine postnatal pancreas and sorted adult ductal progenitor cells.

    “Using aECM-lam, other morphologically-distinct organoids were formed from murine postnatal pancreas194 and sorted adult ductal progenitor cells195.”

    From Towards organoid culture without Matrigel (2021) · cites this paper as [194]

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References 59 · Cited by 9

Authors
Jin, L., Feng, T., Chai, J., Ghazalli, N., Gao, D., Zerda, R., Li, Z., Hsu, J., Mahdavi, A., Tirrell, D. A., Riggs, A. D., & Ku, H. T.
Affiliations
  • City Of Hope National Medical Center (US)
  • California Institute of Technology (US)
Corresponding author
  • Jin, Liang
  • Feng, Tao
  • Chai, Jing
Venue
The Review of Diabetic Studies
Published
2014
Volume
11
Issue
1
Pages
35-50
ISSN
  • 1613-6071 (ISSN-L)
  • 1614-0575
OpenAlex
W6764374
Cited by
9
References
59
Citations by year
2026: 1 · 2024: 1 · 2023: 1 · 2021: 2 · 2019: 1 · 2016: 2 · 2015: 1
FWCI
0.99
Type
journal article
Language
en
Open access
Locations
  • The Review of Diabetic Studies (publishedVersion)
  • Europe PMC (PubMed Central) (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
  • CaltechAUTHORS (California Institute of Technology) (submittedVersion)
Funders
  • National Science Foundation (1206121)
  • California Institute for Regenerative Medicine (RB5-07398)
  • Oxnard Foundation
  • National Institutes of Health (CA 33572)
  • National Cancer Institute (P30CA-33572, P30CA033572)
  • National Institute of Diabetes and Digestive and Kidney Diseases (R01DK099734, R01DK081587, U01DK089533)
  • Division of Materials Research (1206121)
Topics
  • Health Sciences › Medicine › Surgery › Pancreatic function and diabetes
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Pluripotent Stem Cells Research
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
Keywords
colony-forming units, pancreatic progenitor cells, liver progenitor cells, 3D cell culture, Matrigel, extracellular matrix, glucagon, CD133, cell surface markers, islet development
MeSH terms
Animals, Cell Differentiation, Cells, Cultured, Collagen, Colony-Forming Units Assay, Drug Combinations, Insulin, Laminin, Liver, Materials Testing, Mice, Inbred C57BL, Pancreas, Proteoglycans, Gene Expression Regulation, Developmental, Hydrogels, Animals, Outbred Strains, Multipotent Stem Cells, Microscopy, Electron, Transmission, Cell Proliferation, Mice, Adult Stem Cells, Primary Cell Culture

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