Figure 4
Impact of adipocytes on the maintenance of HPCs in vitro. Without frequent media changes and at high cell density, GZL, an established MSC cell line, differentiates preferentially into adipocytes (GZL/Adi). The number of adipocytes is greatly reduced when the cells are propagated under more favorable conditions (GZL). Both GZL and GZL/Adi were used along with primary SCs to sustain LSK cells for 7 days. (A) Cells were harvested on day 7, counted, and used in clonogenic assays. (B) SC, GZL, and GZL/Adi were assayed by quantitative RT-PCR for the expression of adiponectin and FABP4 as indicators of adipogenic differentiation. Data were normalized to primary SCs. (C) SCs, GZL, and GZL/Adi were separated from LSK progeny on day 7 by cell sorting and assayed by quantitative RT-PCR for the expression of neuropilin-1. Expression of Np1 was normalized to primary SCs. P < .05 between SC and GZL/Adi groups in panel A.

Impact of adipocytes on the maintenance of HPCs in vitro. Without frequent media changes and at high cell density, GZL, an established MSC cell line, differentiates preferentially into adipocytes (GZL/Adi). The number of adipocytes is greatly reduced when the cells are propagated under more favorable conditions (GZL). Both GZL and GZL/Adi were used along with primary SCs to sustain LSK cells for 7 days. (A) Cells were harvested on day 7, counted, and used in clonogenic assays. (B) SC, GZL, and GZL/Adi were assayed by quantitative RT-PCR for the expression of adiponectin and FABP4 as indicators of adipogenic differentiation. Data were normalized to primary SCs. (C) SCs, GZL, and GZL/Adi were separated from LSK progeny on day 7 by cell sorting and assayed by quantitative RT-PCR for the expression of neuropilin-1. Expression of Np1 was normalized to primary SCs. P < .05 between SC and GZL/Adi groups in panel A.

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