Immediate but Temporal Response: The Role of Distal Epithelial Cells in Wound Healing.

IF 4.5 3区 医学 Q2 CELL & TISSUE ENGINEERING Stem Cell Reviews and Reports Pub Date : 2024-08-01 Epub Date: 2024-05-17 DOI:10.1007/s12015-024-10734-2
Tyler Thompson, Shannan Flanagan, Dayane Ortega-Gonzalez, Tianli Zhu, Xue Yuan
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Abstract

Efficient oral mucosal wound healing requires coordinated responses from epithelial progenitor cells, yet their spatiotemporal recruitment and activation remain unclear. Using a mouse model of palatal mucosal wound healing, we investigated the dynamics of epithelial cells during this process. Proliferation analysis revealed that, in addition to the expected proliferation center near the wound edge, distal cell populations rapidly activated post-injury by elevating their mitotic activity. These distal cells displayed predominant lateral expansion in the basal layer, suggesting roles beyond just tissue renewal. However, while proximal proliferation center cells sustained heightened proliferation until re-epithelialization was completed, distal cells restored basal turnover rates before wound closure, indicating temporally confined contributions. Lineage tracing of Wnt-responsive epithelial cells showed remarkable clone expansion in basal layers both proximally and distally after wounding, contrasting with gradual clone expansion in homeostasis. Although prioritizing tissue repair, epithelial progenitor cells maintained differentiation programs and barrier functions, with the exception of the leading edge. At the leading edge, we found accelerated cell turnover, but the differentiation program was suspended. In summary, our findings uncovered that oral wound re-epithelialization involves two phases: an initial widespread response with proliferation of proximal and distal cells, followed by proliferation confined to the wound proximal region. Uncovering these stage-specific healing mechanisms provides insights for developing targeted therapeutic strategies to improve wound care.

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即时但有时间性的反应:远端上皮细胞在伤口愈合中的作用
有效的口腔黏膜伤口愈合需要上皮祖细胞的协调反应,但它们的时空招募和激活仍不清楚。我们利用小鼠腭粘膜伤口愈合模型,研究了上皮细胞在这一过程中的动态变化。增殖分析表明,除了靠近伤口边缘的预期增殖中心外,远端细胞群也在受伤后通过提高有丝分裂活性迅速活化。这些远端细胞在基底层显示出主要的横向扩张,表明它们的作用不仅仅是组织更新。然而,虽然近端增殖中心细胞在完成上皮再形成之前一直保持着增殖,但远端细胞在伤口闭合之前就恢复了基底层的更新率,这表明它们的作用是有时间限制的。对 Wnt 反应性上皮细胞的系谱追踪显示,伤口愈合后,基底层细胞在近端和远端都出现了显著的克隆扩张,这与平衡状态下克隆的逐渐扩张形成了鲜明对比。虽然上皮祖细胞优先进行组织修复,但它们仍保持着分化程序和屏障功能,前缘除外。在前缘,我们发现细胞更替加快,但分化程序暂停。总之,我们的发现揭示了口腔伤口再上皮化涉及两个阶段:最初是近端和远端细胞增殖的广泛反应,随后是仅限于伤口近端区域的增殖。揭示这些特定阶段的愈合机制为制定有针对性的治疗策略以改善伤口护理提供了启示。
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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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