Paracrine effects of bone marrow soup restore organ function, regeneration, and repair in salivary glands damaged by irradiation.
BACKGROUND: There are reports that bone marrow cell (BM) transplants repaired irradiated salivary glands (SGs) and re-established saliva secretion. However, the mechanisms of action behind these reports have not been elucidated. METHODS: To test if a paracrine mechanism was the main effect behind th...
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doaj-73dc565af30048f1b3536ddd2a8434ae2020-11-25T01:48:10ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0184e6163210.1371/journal.pone.0061632Paracrine effects of bone marrow soup restore organ function, regeneration, and repair in salivary glands damaged by irradiation.Simon D TranYounan LiuDengsheng XiaOla M MariaSaeed KhaliliRenee Wan-Jou WangVu-Hung QuanShen HuJan SeuntjensBACKGROUND: There are reports that bone marrow cell (BM) transplants repaired irradiated salivary glands (SGs) and re-established saliva secretion. However, the mechanisms of action behind these reports have not been elucidated. METHODS: To test if a paracrine mechanism was the main effect behind this reported improvement in salivary organ function, whole BM cells were lysed and its soluble intracellular contents (termed as "BM Soup") injected into mice with irradiation-injured SGs. The hypothesis was that BM Soup would protect salivary cells, increase tissue neovascularization, function, and regeneration. Two minor aims were also tested a) comparing two routes of delivering BM Soup, intravenous (I.V.) versus intra-glandular injections, and b) comparing the age of the BM Soup's donors. The treatment-comparison group consisted of irradiated mice receiving injections of living whole BM cells. Control mice received irradiation and injections of saline or sham-irradiation. All mice were followed for 8 weeks post-irradiation. RESULTS: BM Soup restored salivary flow rates to normal levels, protected salivary acinar, ductal, myoepithelial, and progenitor cells, increased cell proliferation and blood vessels, and up-regulated expression of tissue remodeling/repair/regenerative genes (MMP2, CyclinD1, BMP7, EGF, NGF). BM Soup was as an efficient therapeutic agent as injections of live BM cells. Both intra-glandular or I.V. injections of BM Soup, and from both young and older mouse donors were as effective in repairing irradiated SGs. The intra-glandular route reduced injection frequency/dosage by four-fold. CONCLUSION: BM Soup, which contains only the cell by-products, can be advantageously used to repair irradiation-damaged SGs rather than transplanting whole live BM cells which carry the risk of differentiating into unwanted/tumorigenic cell types in SGs.http://europepmc.org/articles/PMC3634855?pdf=render |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Simon D Tran Younan Liu Dengsheng Xia Ola M Maria Saeed Khalili Renee Wan-Jou Wang Vu-Hung Quan Shen Hu Jan Seuntjens |
spellingShingle |
Simon D Tran Younan Liu Dengsheng Xia Ola M Maria Saeed Khalili Renee Wan-Jou Wang Vu-Hung Quan Shen Hu Jan Seuntjens Paracrine effects of bone marrow soup restore organ function, regeneration, and repair in salivary glands damaged by irradiation. PLoS ONE |
author_facet |
Simon D Tran Younan Liu Dengsheng Xia Ola M Maria Saeed Khalili Renee Wan-Jou Wang Vu-Hung Quan Shen Hu Jan Seuntjens |
author_sort |
Simon D Tran |
title |
Paracrine effects of bone marrow soup restore organ function, regeneration, and repair in salivary glands damaged by irradiation. |
title_short |
Paracrine effects of bone marrow soup restore organ function, regeneration, and repair in salivary glands damaged by irradiation. |
title_full |
Paracrine effects of bone marrow soup restore organ function, regeneration, and repair in salivary glands damaged by irradiation. |
title_fullStr |
Paracrine effects of bone marrow soup restore organ function, regeneration, and repair in salivary glands damaged by irradiation. |
title_full_unstemmed |
Paracrine effects of bone marrow soup restore organ function, regeneration, and repair in salivary glands damaged by irradiation. |
title_sort |
paracrine effects of bone marrow soup restore organ function, regeneration, and repair in salivary glands damaged by irradiation. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS ONE |
issn |
1932-6203 |
publishDate |
2013-01-01 |
description |
BACKGROUND: There are reports that bone marrow cell (BM) transplants repaired irradiated salivary glands (SGs) and re-established saliva secretion. However, the mechanisms of action behind these reports have not been elucidated. METHODS: To test if a paracrine mechanism was the main effect behind this reported improvement in salivary organ function, whole BM cells were lysed and its soluble intracellular contents (termed as "BM Soup") injected into mice with irradiation-injured SGs. The hypothesis was that BM Soup would protect salivary cells, increase tissue neovascularization, function, and regeneration. Two minor aims were also tested a) comparing two routes of delivering BM Soup, intravenous (I.V.) versus intra-glandular injections, and b) comparing the age of the BM Soup's donors. The treatment-comparison group consisted of irradiated mice receiving injections of living whole BM cells. Control mice received irradiation and injections of saline or sham-irradiation. All mice were followed for 8 weeks post-irradiation. RESULTS: BM Soup restored salivary flow rates to normal levels, protected salivary acinar, ductal, myoepithelial, and progenitor cells, increased cell proliferation and blood vessels, and up-regulated expression of tissue remodeling/repair/regenerative genes (MMP2, CyclinD1, BMP7, EGF, NGF). BM Soup was as an efficient therapeutic agent as injections of live BM cells. Both intra-glandular or I.V. injections of BM Soup, and from both young and older mouse donors were as effective in repairing irradiated SGs. The intra-glandular route reduced injection frequency/dosage by four-fold. CONCLUSION: BM Soup, which contains only the cell by-products, can be advantageously used to repair irradiation-damaged SGs rather than transplanting whole live BM cells which carry the risk of differentiating into unwanted/tumorigenic cell types in SGs. |
url |
http://europepmc.org/articles/PMC3634855?pdf=render |
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