Shushan Moriya, Shoshkes-Carmel Michal
Department of Developmental Biology and Cancer Research, The Hebrew University, Jerusalem 91120, Israel.
Life (Basel). 2022 Jan 26;12(2):176. doi: 10.3390/life12020176.
We recently identified a FOXL1+ intestinal subepithelial network of telocytes (TCs) without which epithelial stem and progenitor cells cannot proliferate and support regeneration. In addition to FOXL1 lineage cell distribution along the intestinal epithelium, we also observed their presence within the muscle layers. Here, we characterized FOXL1+ lineage cells along the muscle layers of the duodenum in order to understand their progeny and relation to interstitial Cajal cells (ICCs), smooth muscle cells (SMCs) and the previously reported PDGFRa+ TCs. Using a FOXL1-Cre transgenic line in conjunction with genetic lineage labeling using the allele, in which Cre-marked cells produce a membrane-targeted version of green fluorescent protein (GFP), we found that within the muscle layers FOXL1 lineage GFP+ cells had two main progeny; (i) elongated multinucleated SMA+ SMCs, intermingled in parallel or perpendicular to muscle fibers. (ii) TCs displaying small cell body with multiple cell processes, expressing PDGFRa and CD34. These findings may suggest a mutual origin for TCs and SMCs.
我们最近发现了一个由端细胞(TCs)构成的FOXL1⁺肠上皮下网络,没有这个网络,上皮干细胞和祖细胞就无法增殖并支持再生。除了FOXL1谱系细胞沿肠上皮分布外,我们还在肌层中观察到它们的存在。在这里,我们对十二指肠肌层中的FOXL1⁺谱系细胞进行了表征,以了解它们的后代以及与间质Cajal细胞(ICCs)、平滑肌细胞(SMCs)和先前报道的PDGFRα⁺ TCs的关系。使用FOXL1-Cre转基因系并结合使用等位基因进行遗传谱系标记,其中Cre标记的细胞产生膜靶向的绿色荧光蛋白(GFP)版本,我们发现在肌层中,FOXL1谱系GFP⁺细胞有两个主要后代;(i)细长的多核SMA⁺ SMCs,与肌纤维平行或垂直混合。(ii)TCs表现为具有多个细胞突起的小细胞体,表达PDGFRα和CD34。这些发现可能表明TCs和SMCs有共同的起源。