Photobiomodulation, alone or combined with adipose-derived stem cells, reduces inflammation by modulation of microRNA-146a and interleukin-1ß in a delayed-healing infected wound in diabetic rats

Diabetic wounds are categorized by chronic inflammation, leading to the development of diabetic foot ulcers, which cause amputation and death. Herewith, we examined the effect of photobiomodulation (PBM) plus allogeneic diabetic adipose tissue-derived stem cells (ad-ADS) on stereological parameters...

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Veröffentlicht in:Lasers in medical science 2023-05, Vol.38 (1), p.129-129, Article 129
Hauptverfasser: Moravej, Fahimeh Ghasemi, Amini, Abdollah, Masteri Farahani, Reza, Mohammadi-Yeganeh, Samira, Mostafavinia, Atarodalsadat, Ahmadi, Houssein, Omidi, Hamidreza, Rezaei, Fatemehalsadat, Gachkar, Latif, Hamblin, Michael R, Chien, Sufan, Bayat, Mohammad
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container_issue 1
container_start_page 129
container_title Lasers in medical science
container_volume 38
creator Moravej, Fahimeh Ghasemi
Amini, Abdollah
Masteri Farahani, Reza
Mohammadi-Yeganeh, Samira
Mostafavinia, Atarodalsadat
Ahmadi, Houssein
Omidi, Hamidreza
Rezaei, Fatemehalsadat
Gachkar, Latif
Hamblin, Michael R
Chien, Sufan
Bayat, Mohammad
description Diabetic wounds are categorized by chronic inflammation, leading to the development of diabetic foot ulcers, which cause amputation and death. Herewith, we examined the effect of photobiomodulation (PBM) plus allogeneic diabetic adipose tissue-derived stem cells (ad-ADS) on stereological parameters and expression levels of interleukin (IL)-1ß and microRNA (miRNA)-146a in the inflammatory (day 4) and proliferation (day 8) stages of wound healing in an ischemic infected (with 2×10 7 colony-forming units of methicillin-resistant Staphylococcus aureus ) delayed healing wound model (IIDHWM) in type I diabetic (TIDM) rats. There were five groups of rats: group 1 control (C); group 2 (CELL) in which rat wounds received 1×10 6 ad-ADS; group 3 (CL) in which rat wounds received the ad-ADS and were subsequently exposed to PBM(890 nm, 80 Hz, 3.5 J/cm 2 , in vivo); group 4 (CP) in which the ad-ADS preconditioned by the PBM(630 nm + 810 nm, 0.05 W, 1.2 J/cm 2 , 3 times) were implanted into rat wounds; group 5 (CLP) in which the PBM preconditioned ad-ADS were implanted into rat wounds, which were then exposed to PBM. On both days, significantly better histological results were seen in all experimental groups except control. Significantly better histological results were observed in the ad-ADS plus PBM treatment correlated to the ad-ADS alone group ( p
doi_str_mv 10.1007/s10103-023-03786-2
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Herewith, we examined the effect of photobiomodulation (PBM) plus allogeneic diabetic adipose tissue-derived stem cells (ad-ADS) on stereological parameters and expression levels of interleukin (IL)-1ß and microRNA (miRNA)-146a in the inflammatory (day 4) and proliferation (day 8) stages of wound healing in an ischemic infected (with 2×10 7 colony-forming units of methicillin-resistant Staphylococcus aureus ) delayed healing wound model (IIDHWM) in type I diabetic (TIDM) rats. There were five groups of rats: group 1 control (C); group 2 (CELL) in which rat wounds received 1×10 6 ad-ADS; group 3 (CL) in which rat wounds received the ad-ADS and were subsequently exposed to PBM(890 nm, 80 Hz, 3.5 J/cm 2 , in vivo); group 4 (CP) in which the ad-ADS preconditioned by the PBM(630 nm + 810 nm, 0.05 W, 1.2 J/cm 2 , 3 times) were implanted into rat wounds; group 5 (CLP) in which the PBM preconditioned ad-ADS were implanted into rat wounds, which were then exposed to PBM. On both days, significantly better histological results were seen in all experimental groups except control. Significantly better histological results were observed in the ad-ADS plus PBM treatment correlated to the ad-ADS alone group ( p &lt;0.05). Overall, PBM preconditioned ad-ADS followed by PBM of the wound showed the most significant improvement in histological measures correlated to the other experimental groups ( p &lt;0.05). On days 4 and 8, IL-1 β levels of all experimental groups were lower than the control group; however, on day 8, only the CLP group was different ( p &lt;0.01). On day 4, miR-146a expression levels were substantially greater in the CLP and CELL groups correlated to the other groups, on day 8 miR-146a in all treatment groups was upper than C ( p &lt;0.01). ad-ADS plus PBM, ad-ADS, and PBM all improved the inflammatory phase of wound healing in an IIDHWM in TIDM1 rats by reducing inflammatory cells (neutrophils, macrophages) and IL-1ß, and increasing miRNA-146a. 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Herewith, we examined the effect of photobiomodulation (PBM) plus allogeneic diabetic adipose tissue-derived stem cells (ad-ADS) on stereological parameters and expression levels of interleukin (IL)-1ß and microRNA (miRNA)-146a in the inflammatory (day 4) and proliferation (day 8) stages of wound healing in an ischemic infected (with 2×10 7 colony-forming units of methicillin-resistant Staphylococcus aureus ) delayed healing wound model (IIDHWM) in type I diabetic (TIDM) rats. There were five groups of rats: group 1 control (C); group 2 (CELL) in which rat wounds received 1×10 6 ad-ADS; group 3 (CL) in which rat wounds received the ad-ADS and were subsequently exposed to PBM(890 nm, 80 Hz, 3.5 J/cm 2 , in vivo); group 4 (CP) in which the ad-ADS preconditioned by the PBM(630 nm + 810 nm, 0.05 W, 1.2 J/cm 2 , 3 times) were implanted into rat wounds; group 5 (CLP) in which the PBM preconditioned ad-ADS were implanted into rat wounds, which were then exposed to PBM. On both days, significantly better histological results were seen in all experimental groups except control. Significantly better histological results were observed in the ad-ADS plus PBM treatment correlated to the ad-ADS alone group ( p &lt;0.05). Overall, PBM preconditioned ad-ADS followed by PBM of the wound showed the most significant improvement in histological measures correlated to the other experimental groups ( p &lt;0.05). On days 4 and 8, IL-1 β levels of all experimental groups were lower than the control group; however, on day 8, only the CLP group was different ( p &lt;0.01). On day 4, miR-146a expression levels were substantially greater in the CLP and CELL groups correlated to the other groups, on day 8 miR-146a in all treatment groups was upper than C ( p &lt;0.01). ad-ADS plus PBM, ad-ADS, and PBM all improved the inflammatory phase of wound healing in an IIDHWM in TIDM1 rats by reducing inflammatory cells (neutrophils, macrophages) and IL-1ß, and increasing miRNA-146a. The ad-ADS+PBM combination was better than either ad-ADS or PBM alone, because of the higher proliferative and anti-inflammatory effects of the PBM+ad-ADS regimen.</description><subject>Adipose tissue</subject><subject>Amputation</subject><subject>Animals</subject><subject>Cytokines</subject><subject>Dentistry</subject><subject>Diabetes</subject><subject>Diabetes mellitus</subject><subject>Diabetes Mellitus, Experimental - pathology</subject><subject>Drug resistance</subject><subject>Inflammation</subject><subject>Inflammation - radiotherapy</subject><subject>Interleukin 1</subject><subject>Ischemia</subject><subject>Lasers</subject><subject>Leukocytes (neutrophilic)</subject><subject>Light therapy</subject><subject>Low-Level Light Therapy - methods</subject><subject>Macrophages</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Methicillin</subject><subject>Methicillin-Resistant Staphylococcus aureus</subject><subject>MicroRNAs</subject><subject>MicroRNAs - genetics</subject><subject>miRNA</subject><subject>Optical Devices</subject><subject>Optics</subject><subject>Original Article</subject><subject>Photonics</subject><subject>Quantum Optics</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Ribonucleic acid</subject><subject>RNA</subject><subject>Staphylococcus infections</subject><subject>Stem cells</subject><subject>Stem Cells - pathology</subject><subject>Ulcers</subject><subject>Wound Healing</subject><issn>1435-604X</issn><issn>0268-8921</issn><issn>1435-604X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9kc1u1DAQxyMEoqXwAhyQJS4c6uKxEzt7rCq-pKogBBK3yLEnXZfEXmyn1T4ND9MXw9ktFHHAkuWP-c3f4_lX1XNgJ8CYep2AAROU8TKFaiXlD6pDqEVDJau_Pfxrf1A9SemKMVASxOPqQChei1bww-r20zrk0LswBTuPOrvgj4keg0cSIjFh6p1HS25cXhNt3SYkpBajuy6XKeNEDI5jOiYR7WwwEeeHUU_TToj0W3IvS8JAJmdi-HxxSqGWmmhvC58xjjh_d57C7c9yJppYHPUWLV2jHp2_XETR5KWMMO9yiHW6x-wMiTqnp9WjQY8Jn92tR9XXt2--nL2n5x_ffTg7PadGqCZTK5XkQ22M1WBL6xBBtkoLLGFty1Bt07QAUkIPzPb1gLzlbTMANjBII46qV3vdTQw_Zky5m1xa_q89hjl1hWaMqxXnBX35D3oV5uhLdYWClZKiXq0KxfdU6UpKEYduE92k47YD1i0Wd3uLu2Jxt7O4W6Rf3EnP_YT2T8pvTwsg9kAqIX-J8f7t_8j-AtNGtWw</recordid><startdate>20230527</startdate><enddate>20230527</enddate><creator>Moravej, Fahimeh Ghasemi</creator><creator>Amini, Abdollah</creator><creator>Masteri Farahani, Reza</creator><creator>Mohammadi-Yeganeh, Samira</creator><creator>Mostafavinia, Atarodalsadat</creator><creator>Ahmadi, Houssein</creator><creator>Omidi, Hamidreza</creator><creator>Rezaei, Fatemehalsadat</creator><creator>Gachkar, Latif</creator><creator>Hamblin, Michael R</creator><creator>Chien, Sufan</creator><creator>Bayat, Mohammad</creator><general>Springer London</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QO</scope><scope>7RV</scope><scope>7SP</scope><scope>7U5</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H8D</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>L7M</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-8921-4045</orcidid><orcidid>https://orcid.org/0000-0002-5314-5022</orcidid><orcidid>https://orcid.org/0000-0001-6431-4605</orcidid><orcidid>https://orcid.org/0000-0002-9408-3200</orcidid><orcidid>https://orcid.org/0000-0001-6721-2153</orcidid><orcidid>https://orcid.org/0000-0003-2270-5637</orcidid><orcidid>https://orcid.org/0000-0001-8748-1270</orcidid><orcidid>https://orcid.org/0000-0001-5214-4223</orcidid><orcidid>https://orcid.org/0000-0003-3878-3082</orcidid><orcidid>https://orcid.org/0000-0002-1067-4178</orcidid><orcidid>https://orcid.org/0000-0002-6300-4143</orcidid><orcidid>https://orcid.org/0000-0001-5699-9907</orcidid></search><sort><creationdate>20230527</creationdate><title>Photobiomodulation, alone or combined with adipose-derived stem cells, reduces inflammation by modulation of microRNA-146a and interleukin-1ß in a delayed-healing infected wound in diabetic rats</title><author>Moravej, Fahimeh Ghasemi ; Amini, Abdollah ; Masteri Farahani, Reza ; Mohammadi-Yeganeh, Samira ; Mostafavinia, Atarodalsadat ; Ahmadi, Houssein ; Omidi, Hamidreza ; Rezaei, Fatemehalsadat ; Gachkar, Latif ; Hamblin, Michael R ; Chien, Sufan ; Bayat, Mohammad</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c375t-d6762f4ccda1d101ee1687a3ec37adddd7855811661b10db4fe28285f1e51f6c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Adipose tissue</topic><topic>Amputation</topic><topic>Animals</topic><topic>Cytokines</topic><topic>Dentistry</topic><topic>Diabetes</topic><topic>Diabetes mellitus</topic><topic>Diabetes Mellitus, Experimental - 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Academic</collection><jtitle>Lasers in medical science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Moravej, Fahimeh Ghasemi</au><au>Amini, Abdollah</au><au>Masteri Farahani, Reza</au><au>Mohammadi-Yeganeh, Samira</au><au>Mostafavinia, Atarodalsadat</au><au>Ahmadi, Houssein</au><au>Omidi, Hamidreza</au><au>Rezaei, Fatemehalsadat</au><au>Gachkar, Latif</au><au>Hamblin, Michael R</au><au>Chien, Sufan</au><au>Bayat, Mohammad</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Photobiomodulation, alone or combined with adipose-derived stem cells, reduces inflammation by modulation of microRNA-146a and interleukin-1ß in a delayed-healing infected wound in diabetic rats</atitle><jtitle>Lasers in medical science</jtitle><stitle>Lasers Med Sci</stitle><addtitle>Lasers Med Sci</addtitle><date>2023-05-27</date><risdate>2023</risdate><volume>38</volume><issue>1</issue><spage>129</spage><epage>129</epage><pages>129-129</pages><artnum>129</artnum><issn>1435-604X</issn><issn>0268-8921</issn><eissn>1435-604X</eissn><abstract>Diabetic wounds are categorized by chronic inflammation, leading to the development of diabetic foot ulcers, which cause amputation and death. Herewith, we examined the effect of photobiomodulation (PBM) plus allogeneic diabetic adipose tissue-derived stem cells (ad-ADS) on stereological parameters and expression levels of interleukin (IL)-1ß and microRNA (miRNA)-146a in the inflammatory (day 4) and proliferation (day 8) stages of wound healing in an ischemic infected (with 2×10 7 colony-forming units of methicillin-resistant Staphylococcus aureus ) delayed healing wound model (IIDHWM) in type I diabetic (TIDM) rats. There were five groups of rats: group 1 control (C); group 2 (CELL) in which rat wounds received 1×10 6 ad-ADS; group 3 (CL) in which rat wounds received the ad-ADS and were subsequently exposed to PBM(890 nm, 80 Hz, 3.5 J/cm 2 , in vivo); group 4 (CP) in which the ad-ADS preconditioned by the PBM(630 nm + 810 nm, 0.05 W, 1.2 J/cm 2 , 3 times) were implanted into rat wounds; group 5 (CLP) in which the PBM preconditioned ad-ADS were implanted into rat wounds, which were then exposed to PBM. On both days, significantly better histological results were seen in all experimental groups except control. Significantly better histological results were observed in the ad-ADS plus PBM treatment correlated to the ad-ADS alone group ( p &lt;0.05). Overall, PBM preconditioned ad-ADS followed by PBM of the wound showed the most significant improvement in histological measures correlated to the other experimental groups ( p &lt;0.05). On days 4 and 8, IL-1 β levels of all experimental groups were lower than the control group; however, on day 8, only the CLP group was different ( p &lt;0.01). On day 4, miR-146a expression levels were substantially greater in the CLP and CELL groups correlated to the other groups, on day 8 miR-146a in all treatment groups was upper than C ( p &lt;0.01). ad-ADS plus PBM, ad-ADS, and PBM all improved the inflammatory phase of wound healing in an IIDHWM in TIDM1 rats by reducing inflammatory cells (neutrophils, macrophages) and IL-1ß, and increasing miRNA-146a. The ad-ADS+PBM combination was better than either ad-ADS or PBM alone, because of the higher proliferative and anti-inflammatory effects of the PBM+ad-ADS regimen.</abstract><cop>London</cop><pub>Springer London</pub><pmid>37243832</pmid><doi>10.1007/s10103-023-03786-2</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0001-8921-4045</orcidid><orcidid>https://orcid.org/0000-0002-5314-5022</orcidid><orcidid>https://orcid.org/0000-0001-6431-4605</orcidid><orcidid>https://orcid.org/0000-0002-9408-3200</orcidid><orcidid>https://orcid.org/0000-0001-6721-2153</orcidid><orcidid>https://orcid.org/0000-0003-2270-5637</orcidid><orcidid>https://orcid.org/0000-0001-8748-1270</orcidid><orcidid>https://orcid.org/0000-0001-5214-4223</orcidid><orcidid>https://orcid.org/0000-0003-3878-3082</orcidid><orcidid>https://orcid.org/0000-0002-1067-4178</orcidid><orcidid>https://orcid.org/0000-0002-6300-4143</orcidid><orcidid>https://orcid.org/0000-0001-5699-9907</orcidid></addata></record>
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identifier ISSN: 1435-604X
ispartof Lasers in medical science, 2023-05, Vol.38 (1), p.129-129, Article 129
issn 1435-604X
0268-8921
1435-604X
language eng
recordid cdi_proquest_miscellaneous_2820027922
source MEDLINE; SpringerLink Journals - AutoHoldings
subjects Adipose tissue
Amputation
Animals
Cytokines
Dentistry
Diabetes
Diabetes mellitus
Diabetes Mellitus, Experimental - pathology
Drug resistance
Inflammation
Inflammation - radiotherapy
Interleukin 1
Ischemia
Lasers
Leukocytes (neutrophilic)
Light therapy
Low-Level Light Therapy - methods
Macrophages
Medicine
Medicine & Public Health
Methicillin
Methicillin-Resistant Staphylococcus aureus
MicroRNAs
MicroRNAs - genetics
miRNA
Optical Devices
Optics
Original Article
Photonics
Quantum Optics
Rats
Rats, Wistar
Ribonucleic acid
RNA
Staphylococcus infections
Stem cells
Stem Cells - pathology
Ulcers
Wound Healing
title Photobiomodulation, alone or combined with adipose-derived stem cells, reduces inflammation by modulation of microRNA-146a and interleukin-1ß in a delayed-healing infected wound in diabetic rats
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