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Conference Paper: Effects of Serotonin on Proplatelet Formation and F-actin Reorganization in Human Megakaryocytes
Title | Effects of Serotonin on Proplatelet Formation and F-actin Reorganization in Human Megakaryocytes |
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Authors | |
Issue Date | 2007 |
Publisher | American Society of Hematology |
Citation | The 49th ASH Annual Meeting, Atlanta, GA, 8-11 December 2007. In Blood, 2007, v. 110 n. 11, p. 2108 How to Cite? |
Abstract | We previously reported that serotonin (5-HT) is a growth factor for hematopoietic stem cells and megakaryocytic progenitor (Yang et al, Stem Cells, 2007). We further proposed a possible role of serotonin on megakaryocyte differentiation and platelet formation. The effect of serotonin on proplatelet formation and F-actin reorganization in human megakaryocytes (MKs) was investigated in this study. Our results showed that:
There was a stimulating effect of serotonin on proplatelet formation in human bone marrow megakaryocytes. Human BM MK progenitors cultured in serum free medium with either 5-HT (200nM) or TPO (50 ng/ml) had more proplatelet bearing MKs than the control group (5-HT(11.33% ± 4.93) vs. control (6% ± 3.60), P=0.026; TPO (14.66% ± 1.53) vs. control, P=0.043; n=3). The 5-HT treatment group showed more mature and more in the final stage MK cells as compared to TPO group;
The effect of serotonin on proplatelet formation in Meg-01 cells were via 5-HT2 receptors. Meg-01 cells strongly expressed 5-HT 2A, 2B, 2C receptors by using western blot method. 5-HT also promoted proplatelet formation in these cells and this effect was reduced by 5-HT2 receptor inhibitor ketanserin (KE); and
Serotonin acted on cytoskeleton reorganization in human megakaryocytes via 5-HT2 receptors and ERK1/2 pathway.
Using an immunofluorescence microscope with F-actin specific binder rhodamine-phalloidin staining, the polymerized actin level was lower in the control group (serum free) than the 5-HT group and actin distributed diffusely throughout the cytoplasm. In contrast, polymerization actin level was higher in 5-HT group. Adding ketanserin and ERK1/2 inhibitor PD98059 to 5-HT treatment, the fluorescence intensity was correspondingly reduced (5HT vs. Control, P=0.006; 5-HT vs.5-HT plus KE, P=0.014; n=6). Our data also demonstrated that ERK1/2 was activated in MK cells treated with 5-HT for 30 minutes (21.76% ± 7.42). Our studies showed that serotonin had a stimulating effect on proplatelet formation and F-actin reorganization in human megakaryocytes and this effect involved the 5-HT2 receptors and the activation of ERK1/2 pathway. |
Persistent Identifier | http://hdl.handle.net/10722/106218 |
ISSN | 2023 Impact Factor: 21.0 2023 SCImago Journal Rankings: 5.272 |
DC Field | Value | Language |
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dc.contributor.author | Cheng, YS | en_HK |
dc.contributor.author | Liu, YS | en_HK |
dc.contributor.author | Chan, GCF | en_HK |
dc.contributor.author | Ye, JY | en_HK |
dc.contributor.author | Lau, YL | en_HK |
dc.contributor.author | Yang, M | en_HK |
dc.date.accessioned | 2010-09-25T23:06:33Z | - |
dc.date.available | 2010-09-25T23:06:33Z | - |
dc.date.issued | 2007 | en_HK |
dc.identifier.citation | The 49th ASH Annual Meeting, Atlanta, GA, 8-11 December 2007. In Blood, 2007, v. 110 n. 11, p. 2108 | en_HK |
dc.identifier.issn | 0006-4971 | - |
dc.identifier.uri | http://hdl.handle.net/10722/106218 | - |
dc.description.abstract | We previously reported that serotonin (5-HT) is a growth factor for hematopoietic stem cells and megakaryocytic progenitor (Yang et al, Stem Cells, 2007). We further proposed a possible role of serotonin on megakaryocyte differentiation and platelet formation. The effect of serotonin on proplatelet formation and F-actin reorganization in human megakaryocytes (MKs) was investigated in this study. Our results showed that: There was a stimulating effect of serotonin on proplatelet formation in human bone marrow megakaryocytes. Human BM MK progenitors cultured in serum free medium with either 5-HT (200nM) or TPO (50 ng/ml) had more proplatelet bearing MKs than the control group (5-HT(11.33% ± 4.93) vs. control (6% ± 3.60), P=0.026; TPO (14.66% ± 1.53) vs. control, P=0.043; n=3). The 5-HT treatment group showed more mature and more in the final stage MK cells as compared to TPO group; The effect of serotonin on proplatelet formation in Meg-01 cells were via 5-HT2 receptors. Meg-01 cells strongly expressed 5-HT 2A, 2B, 2C receptors by using western blot method. 5-HT also promoted proplatelet formation in these cells and this effect was reduced by 5-HT2 receptor inhibitor ketanserin (KE); and Serotonin acted on cytoskeleton reorganization in human megakaryocytes via 5-HT2 receptors and ERK1/2 pathway. Using an immunofluorescence microscope with F-actin specific binder rhodamine-phalloidin staining, the polymerized actin level was lower in the control group (serum free) than the 5-HT group and actin distributed diffusely throughout the cytoplasm. In contrast, polymerization actin level was higher in 5-HT group. Adding ketanserin and ERK1/2 inhibitor PD98059 to 5-HT treatment, the fluorescence intensity was correspondingly reduced (5HT vs. Control, P=0.006; 5-HT vs.5-HT plus KE, P=0.014; n=6). Our data also demonstrated that ERK1/2 was activated in MK cells treated with 5-HT for 30 minutes (21.76% ± 7.42). Our studies showed that serotonin had a stimulating effect on proplatelet formation and F-actin reorganization in human megakaryocytes and this effect involved the 5-HT2 receptors and the activation of ERK1/2 pathway. | - |
dc.language | eng | en_HK |
dc.publisher | American Society of Hematology | - |
dc.relation.ispartof | Blood | en_HK |
dc.title | Effects of Serotonin on Proplatelet Formation and F-actin Reorganization in Human Megakaryocytes | en_HK |
dc.type | Conference_Paper | en_HK |
dc.identifier.email | Chan, GCF: gcfchan@hkucc.hku.hk | en_HK |
dc.identifier.email | Lau, YL: lauylung@hkucc.hku.hk | en_HK |
dc.identifier.email | Yang, M: yangm1091@yahoo.com.hk | en_HK |
dc.identifier.authority | Chan, GCF=rp00431 | en_HK |
dc.identifier.authority | Lau, YL=rp00361 | en_HK |
dc.identifier.hkuros | 139770 | en_HK |
dc.identifier.volume | 110 | en_HK |
dc.identifier.issue | 11 | en_HK |
dc.identifier.spage | 2108 | en_HK |
dc.identifier.issnl | 0006-4971 | - |