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. 2015 Feb 26;10(2):e0117352. doi: 10.1371/journal.pone.0117352

Fig 3. Expression of markers for mature lymphatic endothelial cells in isolated CD133+ and CD133− LM cells.

Fig 3

(A) Podoplanin, VE-cadherin, VEGFR-2, VEGFR-3, Prox1, and LYVE1 qRT-PCR of RNA isolated from CD133+ and CD133− cells from LMs of different subtypes and anatomical locations and GLA compared to control HdLECs. Data normalized to β-actin qRT-PCR and represented as mean ± s.e.m. (B) CD31 and VE-cadherin FACS of patient-matched CD133+ and CD133− LM cells isolated from microcystic mesenteric (Micro Mes) LM, microcystic subcutaneous (Micro SC) LM and general lymphatic anomaly (GLA) specimens. Thick gray line represents antibody data, and black line IgG control. (C) VE-cadherin/CD31 and (D) podoplanin/LYVE1 staining of patient-matched CD133+ and CD133− LM cells isolated from microcystic mesenteric (Micro Mes) LM, microcystic subcutaneous (Micro SC) LM, and GLA compared to control HdLEC. Scale bars: 50μm.