دورية أكاديمية

Salivary Gland Tissue Recombination Can Modify Cell Fate.

التفاصيل البيبلوغرافية
العنوان: Salivary Gland Tissue Recombination Can Modify Cell Fate.
المؤلفون: Sekiguchi R; Cell Biology Section, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD, USA., Martin D; Genomics and Computational Biology Core, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD, USA., Doyle AD; Cell Biology Section, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD, USA.; Imaging Core, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD, USA., Wang S; Cell Biology Section, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD, USA.; Janelia Research Campus, Howard Hughes Medical Institute, Ashburn, VA, USA., Yamada KM; Cell Biology Section, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD, USA.
مؤلفون مشاركون: Genomics and Computational Biology Core; National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD, USA.
المصدر: Journal of dental research [J Dent Res] 2024 Jul; Vol. 103 (7), pp. 755-764. Date of Electronic Publication: 2024 May 07.
نوع المنشور: Journal Article
اللغة: English
بيانات الدورية: Publisher: Sage Country of Publication: United States NLM ID: 0354343 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1544-0591 (Electronic) Linking ISSN: 00220345 NLM ISO Abbreviation: J Dent Res Subsets: MEDLINE
أسماء مطبوعة: Publication: Thousand Oaks, CA : Sage
Original Publication: Chicago, American Dental Assn. [etc.]
مواضيع طبية MeSH: Cell Differentiation* , Submandibular Gland*/embryology , Submandibular Gland*/cytology , Mesoderm*/cytology , Mesoderm*/embryology, Animals ; Mice ; Parotid Gland/cytology ; Parotid Gland/embryology ; Parotid Gland/metabolism ; Epithelial Cells ; Salivary Glands/embryology ; Salivary Glands/cytology ; Cell Lineage ; Acinar Cells ; Epithelium/embryology
مستخلص: Although mesenchyme is essential for inducing the epithelium of ectodermal organs, its precise role in organ-specific epithelial fate determination remains poorly understood. To elucidate the roles of tissue interactions in cellular differentiation, we performed single-cell RNA sequencing and imaging analyses on recombined tissues, where mesenchyme and epithelium were switched ex vivo between two types of embryonic mouse salivary glands: the parotid gland (a serous gland) and the submandibular gland (a predominantly mucous gland). We found partial induction of molecules that define gland-specific acinar and myoepithelial cells in recombined salivary epithelium. The parotid epithelium recombined with submandibular mesenchyme began to express mucous acinar genes not intrinsic to the parotid gland. While myoepithelial cells do not normally line parotid acini, newly induced myoepithelial cells densely populated recombined parotid acini. However, mucous acinar and myoepithelial markers continued to be expressed in submandibular epithelial cells recombined with parotid mesenchyme. Consequently, some epithelial cells appeared to be plastic, such that their fate could still be modified in response to mesenchymal signaling, whereas other epithelial cells appeared to be already committed to a specific fate. We also discovered evidence for bidirectional induction: transcriptional changes were observed not only in the epithelium but also in the mesenchyme after heterotypic tissue recombination. For example, parotid epithelium induced the expression of muscle-related genes in submandibular fibroblasts that began to mimic parotid fibroblast gene expression. These studies provide the first comprehensive unbiased molecular characterization of tissue recombination approaches exploring the regulation of cell fate.
Competing Interests: Declaration of Conflicting InterestsThe authors declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.
References: Nature. 2008 Jun 5;453(7196):745-50. (PMID: 18463632)
Biol Open. 2013 Aug 09;2(10):981-9. (PMID: 24167707)
Biochem Biophys Res Commun. 2000 Nov 2;277(3):643-9. (PMID: 11062007)
Radiother Oncol. 1986 Oct;7(2):165-74. (PMID: 3786822)
J Dent Res. 2020 Jan;99(1):69-78. (PMID: 31644367)
Genes Dev. 1998 Oct 15;12(20):3156-61. (PMID: 9784490)
Development. 2002 Dec;129(24):5767-78. (PMID: 12421715)
iScience. 2020 Nov 20;23(12):101838. (PMID: 33305192)
Science. 1976 Dec 24;194(4272):1439-41. (PMID: 827022)
Cell. 2021 Jul 22;184(15):3852-3872. (PMID: 34297930)
Science. 2010 Sep 24;329(5999):1645-7. (PMID: 20929848)
Physiol Genomics. 2018 Apr 1;50(4):263-271. (PMID: 29373073)
Proteomics. 2019 Oct;19(20):e1900023. (PMID: 31476108)
J Dent Res. 2019 Sep;98(10):1122-1130. (PMID: 31356755)
Science. 2016 Dec 23;354(6319):. (PMID: 28008008)
Cell. 2006 Aug 25;126(4):663-76. (PMID: 16904174)
NPJ Regen Med. 2023 Mar 25;8(1):17. (PMID: 36966175)
Proc Natl Acad Sci U S A. 1978 Jun;75(6):2790-4. (PMID: 275848)
Elife. 2017 May 11;6:. (PMID: 28492365)
Mol Ther Methods Clin Dev. 2020 Jul 31;18:839-855. (PMID: 32953934)
Breast Cancer Res. 2011 Aug 11;13(4):R79. (PMID: 21834968)
Nat Commun. 2019 Sep 13;10(1):4182. (PMID: 31519911)
BMC Dev Biol. 2005 Jun 22;5:11. (PMID: 15972105)
J Cell Biol. 1983 Jun;96(6):1662-70. (PMID: 6853597)
Exp Cell Res. 2022 Jul 1;416(1):113137. (PMID: 35427599)
Gastroenterology. 2009 Dec;137(6):2052-62. (PMID: 19737569)
Proc Natl Acad Sci U S A. 2010 Mar 9;107(10):4601-6. (PMID: 20176958)
Science. 1953 Jul 10;118(3054):52-5. (PMID: 13076182)
Breast Cancer Res. 2004;6(6):R605-15. (PMID: 15535842)
Anat Rec. 1972 Jun;173(2):205-12. (PMID: 5033771)
Development. 2005 Mar;132(6):1223-34. (PMID: 15716343)
Development. 2022 Mar 15;149(6):. (PMID: 35224622)
Development. 2011 Jul;138(13):2681-91. (PMID: 21652647)
Cells. 2019 Aug 26;8(9):. (PMID: 31455013)
Nature. 2003 Jun 19;423(6942):876-81. (PMID: 12815434)
Nat Commun. 2018 Oct 11;9(1):4216. (PMID: 30310071)
Nature. 2008 Oct 2;455(7213):627-32. (PMID: 18754011)
Nat Genet. 2005 Feb;37(2):125-7. (PMID: 15654336)
Acta Histochem Cytochem. 2016 Dec 28;49(6):159-169. (PMID: 28127104)
Dev Cell. 2022 Nov 21;57(22):2550-2565.e5. (PMID: 36413949)
معلومات مُعتمدة: Z01 DE000525 United States ImNIH Intramural NIH HHS; R01 DC000086 United States DC NIDCD NIH HHS; ZIC DC000086 United States ImNIH Intramural NIH HHS; ZIG DE000740 United States ImNIH Intramural NIH HHS; ZIA DE000525 United States ImNIH Intramural NIH HHS; ZIC DE000750 United States ImNIH Intramural NIH HHS
فهرسة مساهمة: Keywords: developmental biology; epithelial-mesenchymal interaction; gene expression; morphogenesis; salivary physiology; single cell RNAseq
تواريخ الأحداث: Date Created: 20240508 Date Completed: 20240620 Latest Revision: 20240623
رمز التحديث: 20240623
مُعرف محوري في PubMed: PMC11191754
DOI: 10.1177/00220345241247484
PMID: 38715201
قاعدة البيانات: MEDLINE
الوصف
تدمد:1544-0591
DOI:10.1177/00220345241247484