Pancreatic Differentiation of Oral Minor Salivary Gland Stem Cells.

IF 4.5 3区 医学 Q2 CELL & TISSUE ENGINEERING Stem Cell Reviews and Reports Pub Date : 2024-10-01 Epub Date: 2024-07-05 DOI:10.1007/s12015-024-10757-9
Achilleia-Maria Pavlou, Eleni Papachristou, Ioannis Bonovolias, Eleftherios Anagnostou, Pinelopi Anastasiadou, Athanasios Poulopoulos, Athina Bakopoulou, Dimitrios Andreadis
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Abstract

Introduction: Stem cells from various sources including major salivary glands have been used to establish pancreatic differentiation in an attempt to provide new treatment options for patients with diabetes mellitus. In contrast, the potential of using the more easily accessible intraoral minor salivary glands has not been evaluated so far.

Materials and methods: Salivary stem cells were isolated from normal labial minor salivary glands that were removed during the excision of a mucocele and were attempted to differentiate into pancreatic cell lines using a culture medium enriched with activin A, retinoic acid and GLP-1.Real time RT-PCR was used to evaluate the expression of the genes of pancreatic transcription factors MafA, Ptf1a, Hb9 and Arx. Complementary, 22 labial minor salivary gland paraffin-embedded specimens were examined using immunohistochemistry for the presence of the relevant gene products of the pancreatic transcription factors Arx, MafA, Ptf1a and Pdx1.

Results: The differentiated salivary stem cells(cells of passage 3) expressed the genes of the pancreatic transcription factors MafA, Ptf1a, Hb9 and Arx even on the first day of the experiment while immunohistochemistry also confirmed the presence of the protein products of Arx, MafA, Ptf1a as well as Pdx1[> 50% of the specimens for Arx(5/8) and MafA(7/8), < 50% for Ptf1a(5/11) and Pdx1(5/11)] in ducts, mesenchymal connective tissue and acinar cells.

Conclusions: Labial minor salivary glands may share gene and protein characteristics with pancreas suggesting a possible usefulness for pancreatic regeneration or substitution in cases of deficiency.

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口腔小唾液腺干细胞的胰腺分化。
导言:包括主要唾液腺在内的各种来源的干细胞已被用于建立胰腺分化,试图为糖尿病患者提供新的治疗方案。相比之下,利用口腔内更容易获取的小唾液腺的潜力迄今尚未得到评估:从切除粘液瘤时摘除的正常唇小唾液腺中分离唾液干细胞,并尝试使用富含活化素A、维甲酸和GLP-1的培养基分化成胰腺细胞系。此外,还使用免疫组化方法检测了22个唇小唾液腺石蜡包埋标本中是否存在胰腺转录因子Arx、MafA、Ptf1a和Pdx1的相关基因产物:结果:已分化的唾液干细胞(3期细胞)甚至在实验的第一天就表达了胰腺转录因子MafA、Ptf1a、Hb9和Arx的基因,而免疫组化也证实了Arx、MafA、Ptf1a和Pdx1蛋白产物的存在[Arx(5/8)和MafA(7/8)的标本超过50%,结论:唇侧小唾液腺可能与胰腺具有相同的基因和蛋白质特征,这表明在缺乏胰腺的病例中,唇侧小唾液腺可能有助于胰腺再生或替代胰腺。
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来源期刊
Stem Cell Reviews and Reports
Stem Cell Reviews and Reports 医学-细胞生物学
CiteScore
9.30
自引率
4.20%
发文量
0
审稿时长
3 months
期刊介绍: The purpose of Stem Cell Reviews and Reports is to cover contemporary and emerging areas in stem cell research and regenerative medicine. The journal will consider for publication: i) solicited or unsolicited reviews of topical areas of stem cell biology that highlight, critique and synthesize recent important findings in the field. ii) full length and short reports presenting original experimental work. iii) translational stem cell studies describing results of clinical trials using stem cells as therapeutics. iv) papers focused on diseases of stem cells. v) hypothesis and commentary articles as opinion-based pieces in which authors can propose a new theory, interpretation of a controversial area in stem cell biology, or a stem cell biology question or paradigm. These articles contain more speculation than reviews, but they should be based on solid rationale. vi) protocols as peer-reviewed procedures that provide step-by-step descriptions, outlined in sufficient detail, so that both experts and novices can apply them to their own research. vii) letters to the editor and correspondence. In order to facilitate this exchange of scientific information and exciting novel ideas, the journal has created five thematic sections, focusing on: i) the role of adult stem cells in tissue regeneration; ii) progress in research on induced pluripotent stem cells, embryonic stem cells and mechanism governing embryogenesis and tissue development; iii) the role of microenvironment and extracellular microvesicles in directing the fate of stem cells; iv) mechanisms of stem cell trafficking, stem cell mobilization and homing with special emphasis on hematopoiesis; v) the role of stem cells in aging processes and cancerogenesis.
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