Identification and characterisation of maternal perivascular SUSD2+ placental mesenchymal stem/stromal cells

Mesenchymal stem cells (MSCs) that meet the International Society for Cellular Therapy (ISCT) criteria are obtained from placental tissue by plastic adherence. Historically, no known single marker was available for isolating placental MSCs (pMSCs) from the decidua basalis. As the decidua basalis is derived from the regenerative endometrium, we hypothesised that SUSD2, an endometrial perivascular MSC marker, would purify maternal perivascular pMSC. Perivascular pMSCs were isolated from the maternal placenta using SUSD2 magnetic bead sorting and assessed for the colony-forming unit-fibroblasts (CFU-F), surface markers, and in vitro differentiation into mesodermal lineages. Multi-colour immunofluorescence was used to colocalise SUSD2 and alpha-SMA, a perivascular marker in the decidua basalis. Placental stromal cell suspensions comprised 5.1%SUSD2(+) cells. SUSD2 magnetic bead sorting of the placental stromal cells increased their purity approximately two-fold. SUSD2(+) pMSCs displayed greater CFU-F activity than SUSD2(-) stromal fibroblasts (pSFs). However, both SUSD2(+) pMSC and SUSD2(-) pSF underwent mesodermal differentiation in vitro, and both expressed the ISCT surface markers. Higher percentages of cultured SUSD2(+) pMSCs expressed the perivascular markers CD146, CD140b, and SUSD2 than SUSD2(-) pSFs. These findings suggest that SUSD2 is a single marker that enriches maternal pMSCs, suggesting they may originate from eMSC. Placental decidua basalis can be used as an alternative source of MSC for clinical translation in situations where there is no access to endometrial tissue.

Automated summary

SUSD2 marker can enrich maternal pMSCs, originating potentially from eMSCs. SUSD2(+) pMSCs exhibit higher CFU-F activity and express more perivascular markers CD146, CD140b, and SUSD2 compared to SUSD2(-) pSFs. Placental decidua basalis can serve as an alternative MSC source for clinical translation when endometrial tissue is inaccessible.