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. 2013 Mar 5;121(17):3345–3363. doi: 10.1182/blood-2012-06-439661

Table 6.

Frequency of progenitor cells, erythroid cells, and MK precursors in the BM and spleen of vehicle- and SB431542-treated Gata1low mice

Wild type Gata1low
Untreated Vehicle treated SB431542 treated
CD117pos
 BM 9.8 ± 3.5 3.5 ± 1.2* 6.5 ± 1.9 7.8 ± 1.1†
 Spleen 0.2 ± 0.5 4.6 ± 2.1* 6.6 ± 2.1 11.5 ± 2.1†
CD71pos/Ter119pos, %
 BM 19.3 ± 8.1 13.9 ± 4.3 14.7 ± 1.6 26.7 ± 2.8†
 Spleen 8.5 ± 2.9 14.2 ± 5.5* 12.7 ± 3.6 13.2 ± 2.3
CD41pos/CD61neg, %
 BM 9.9 ± 5.8 30.5 ± 8.7* 30.9 ± 3.1 28.8 ± 4.6
 Spleen 12.8 ± 5.7 23.7 ± 3.1* b.d.‡ b.d.‡
CD41pos/CD61pos, %
 BM 3.8 ± 1.0 8.1 ± 2.5* 14.5 ± 4.7 10.6 ± 3.4
 Spleen 2.3 ± 1.1 19.4 ± 2.3* 16.7 ± 3.4 10.7 ± 3.0‡

Data are presented as mean (±SD) of 3-6 determinations per experimental point. MK precursors were defined as CD41pos cells and divided into immature (CD61neg) and mature (CD61pos) MKs. *, †, and ‡, P < 0.05 between untreated Gata1low and wild-type mice, SB431542- and vehicle-treated Gata1low mice, or treated and untreated Gata1low mice, respectively. The cloning efficiency of CD117pos cells prospectively isolated from vehicle- and SB431542-treated animals was 55 ± 12 vs 44 ± 5 CFC/103 plated cells, respectively.

b.d., below detection.