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Study · In vitro (cells) · 2015

11 results

Controlled release of thymosin beta 4 using a collagen-chitosan sponge scaffold augments cutaneous wound healing and increases angiogenesis in diabetic rats with hindlimb ischemia.

Ti D, Hao H, Xia L, Tong C, Liu J, Dong L, Xu S, Zhao Y, Liu H, Fu X, Han W

Tissue engineering. Part A14 Oct 2014Cited by 35 (Europe PMC)

Summary

The text of this summary is not shown here, because the article license does not allow reuse. Read it at the source (opens in a new tab)

Text rights: Publisher copyright. Results still quote short attributed sentences.

Results from this study11

3 results from studies that gave the peptide. No result from this study comes from people.

  1. 01LabIn vitro (cells)Activity measurement

    In high glucose-treated human umbilical vein endothelial cells, Tβ4 increased migratory activity.

    In plain wordsIn cells, Tβ4 increased the movement of blood vessel cells exposed to high glucose.

    Outcome
    IncreaseHUVEC migration under high glucose
    Study

    humann: not reported in source

    High glucose-treated HUVECs
    Outcome group
    Wound healing · Skin and wound
    Studied dose
    Dose not stated

    Source sentences

    Summary
    In vitro, Tβ4 increased the migratory and proliferative activity of high glucose (HG)-treated human umbilical vein endothelial cells (HUVECs).
    1 context sentence
    Summary · context
    This study investigates the possible use of a collagen-chitosan sponge scaffold encapsulated with thymosin beta 4 (CCSS-eTβ4), an angiogenic factor, to accelerate cutaneous wound healing in streptozotocin (STZ)-induced diabetic rats with hindlimb ischemia.
  2. 02LabIn vitro (cells)Activity measurement

    In high glucose-treated human umbilical vein endothelial cells, Tβ4 increased proliferative activity.

    In plain wordsIn cells, Tβ4 increased the growth of blood vessel cells exposed to high glucose.

    Outcome
    IncreaseHUVEC proliferation under high glucose
    Study

    humann: not reported in source

    High glucose-treated HUVECs
    Outcome group
    Wound healing · Skin and wound
    Studied dose
    Dose not stated

    Source sentences

    Summary
    In vitro, Tβ4 increased the migratory and proliferative activity of high glucose (HG)-treated human umbilical vein endothelial cells (HUVECs).
    1 context sentence
    Summary · context
    This study investigates the possible use of a collagen-chitosan sponge scaffold encapsulated with thymosin beta 4 (CCSS-eTβ4), an angiogenic factor, to accelerate cutaneous wound healing in streptozotocin (STZ)-induced diabetic rats with hindlimb ischemia.
  3. 03LabIn vitro (cells)Mechanism

    In high glucose-treated HUVECs, Tβ4 promoted migration and improved angiogenesis through activation of the VEGF/AKT pathway.

    In plain wordsIn cells, Tβ4 helped blood vessel cells move and form vessels by switching on the VEGF/AKT pathway.

    Outcome
    IncreaseVEGF/AKT pathway activation
    Study

    humann: not reported in source

    High glucose-treated HUVECs
    Outcome group
    Receptor activity and mechanism · Skin and wound
    Studied dose
    Dose not stated

    Source sentences

    Summary
    Meanwhile, we found that Tβ4 could promote HG-treated HUVECs migration and improve angiogenesis by activation of the VEGF/AKT pathway.
    1 context sentence
    Summary · context
    This study investigates the possible use of a collagen-chitosan sponge scaffold encapsulated with thymosin beta 4 (CCSS-eTβ4), an angiogenic factor, to accelerate cutaneous wound healing in streptozotocin (STZ)-induced diabetic rats with hindlimb ischemia.

Studies that did not test the peptide alone8

In this study, Thymosin beta-4 (human) was a lab tool or a carrier, part of a mix, or the subject of a lab method. These results are not evidence about taking Thymosin beta-4 (human).

  1. 04AnimalNot a test of Thymosin beta-4 (human) aloneAnimal study (in vivo)Efficacy outcome

    In diabetic rats with hindlimb ischemia, the Tβ4 scaffold improved cutaneous wound healing with faster wound reepithelialization.

    In plain wordsIn diabetic rats with poor limb blood flow, a sponge that slowly releases Tβ4 sped up skin regrowth over wounds.

    Outcome
    IncreaseWound reepithelialization
    Study

    ratn: not reported in source

    STZ-induced diabetic rats with hindlimb ischemia
    Outcome group
    Wound healing · Skin and wound

    Source sentences

    Summary
    In vivo, CCSSs-eTβ4 improved diabetic cutaneous wound healing, with faster wound reepithelialization, better dermal reorganization, and higher wound vascularization.
    1 context sentence
    Summary · context
    This study investigates the possible use of a collagen-chitosan sponge scaffold encapsulated with thymosin beta 4 (CCSS-eTβ4), an angiogenic factor, to accelerate cutaneous wound healing in streptozotocin (STZ)-induced diabetic rats with hindlimb ischemia.

    In this study, Thymosin beta-4 (human) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Thymosin beta-4 (human).

  2. 05AnimalNot a test of Thymosin beta-4 (human) aloneAnimal study (in vivo)Efficacy outcome

    In diabetic rats with hindlimb ischemia, the Tβ4 scaffold improved cutaneous wound healing with better dermal reorganization.

    In plain wordsIn diabetic rats with poor limb blood flow, a sponge that slowly releases Tβ4 improved the rebuilding of the deeper skin layer.

    Outcome
    IncreaseDermal reorganization
    Study

    ratn: not reported in source

    STZ-induced diabetic rats with hindlimb ischemia
    Outcome group
    Wound healing · Skin and wound

    Source sentences

    Summary
    In vivo, CCSSs-eTβ4 improved diabetic cutaneous wound healing, with faster wound reepithelialization, better dermal reorganization, and higher wound vascularization.
    1 context sentence
    Summary · context
    This study investigates the possible use of a collagen-chitosan sponge scaffold encapsulated with thymosin beta 4 (CCSS-eTβ4), an angiogenic factor, to accelerate cutaneous wound healing in streptozotocin (STZ)-induced diabetic rats with hindlimb ischemia.

    In this study, Thymosin beta-4 (human) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Thymosin beta-4 (human).

  3. 06AnimalNot a test of Thymosin beta-4 (human) aloneAnimal study (in vivo)Efficacy outcome

    In diabetic rats with hindlimb ischemia, the Tβ4 scaffold improved cutaneous wound healing with higher wound vascularization.

    In plain wordsIn diabetic rats with poor limb blood flow, a sponge that slowly releases Tβ4 increased blood vessels in wounds.

    Outcome
    IncreaseWound vascularization
    Study

    ratn: not reported in source

    STZ-induced diabetic rats with hindlimb ischemia
    Outcome group
    Wound healing · Skin and wound

    Source sentences

    Summary
    In vivo, CCSSs-eTβ4 improved diabetic cutaneous wound healing, with faster wound reepithelialization, better dermal reorganization, and higher wound vascularization.
    1 context sentence
    Summary · context
    This study investigates the possible use of a collagen-chitosan sponge scaffold encapsulated with thymosin beta 4 (CCSS-eTβ4), an angiogenic factor, to accelerate cutaneous wound healing in streptozotocin (STZ)-induced diabetic rats with hindlimb ischemia.

    In this study, Thymosin beta-4 (human) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Thymosin beta-4 (human).

  4. 07AnimalNot a test of Thymosin beta-4 (human) aloneAnimal study (in vivo)Efficacy outcome

    In diabetic rats, the Tβ4 scaffold downregulated inflammatory genes in wound tissue.

    In plain wordsIn diabetic rats, a sponge that slowly releases Tβ4 turned down inflammation genes in wound tissue.

    Outcome
    DecreaseInflammatory gene expression in wound tissue
    Study

    ratn: not reported in source

    STZ-induced diabetic rats with hindlimb ischemia
    Outcome group
    Inflammation markers · Skin and wound

    Source sentences

    Summary
    Furthermore, CCSSs-eTβ4 downregulated inflammatory genes and upregulated angiogenic genes in the wound tissue.
    1 context sentence
    Summary · context
    This study investigates the possible use of a collagen-chitosan sponge scaffold encapsulated with thymosin beta 4 (CCSS-eTβ4), an angiogenic factor, to accelerate cutaneous wound healing in streptozotocin (STZ)-induced diabetic rats with hindlimb ischemia.

    In this study, Thymosin beta-4 (human) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Thymosin beta-4 (human).

  5. 08AnimalNot a test of Thymosin beta-4 (human) aloneAnimal study (in vivo)Efficacy outcome

    In diabetic rats, the Tβ4 scaffold upregulated angiogenic genes in wound tissue.

    In plain wordsIn diabetic rats, a sponge that slowly releases Tβ4 turned up genes for blood vessel growth in wound tissue.

    Outcome
    IncreaseAngiogenic gene expression in wound tissue
    Study

    ratn: not reported in source

    STZ-induced diabetic rats with hindlimb ischemia
    Outcome group
    Wound healing · Skin and wound

    Source sentences

    Summary
    Furthermore, CCSSs-eTβ4 downregulated inflammatory genes and upregulated angiogenic genes in the wound tissue.
    1 context sentence
    Summary · context
    This study investigates the possible use of a collagen-chitosan sponge scaffold encapsulated with thymosin beta 4 (CCSS-eTβ4), an angiogenic factor, to accelerate cutaneous wound healing in streptozotocin (STZ)-induced diabetic rats with hindlimb ischemia.

    In this study, Thymosin beta-4 (human) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Thymosin beta-4 (human).

  6. 09AnimalNot a test of Thymosin beta-4 (human) aloneAnimal study (in vivo)Efficacy outcome

    In diabetic rats, the Tβ4 scaffold significantly increased CD31-positive endothelial cells in wound tissue.

    In plain wordsIn diabetic rats, a sponge that slowly releases Tβ4 clearly increased CD31-positive blood vessel lining cells in wounds.

    Outcome
    IncreaseCD31-positive endothelial cells in wound
    Study

    ratn: not reported in source

    STZ-induced diabetic rats with hindlimb ischemia
    Outcome group
    Wound healing · Skin and wound

    Source sentences

    Summary
    Significant increases in CD31-positive endothelial cells and new vessel density were also observed.
    1 context sentence
    Summary · context
    This study investigates the possible use of a collagen-chitosan sponge scaffold encapsulated with thymosin beta 4 (CCSS-eTβ4), an angiogenic factor, to accelerate cutaneous wound healing in streptozotocin (STZ)-induced diabetic rats with hindlimb ischemia.

    In this study, Thymosin beta-4 (human) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Thymosin beta-4 (human).

  7. 10AnimalNot a test of Thymosin beta-4 (human) aloneAnimal study (in vivo)Efficacy outcome

    In diabetic rats, the Tβ4 scaffold significantly increased new vessel density in wound tissue.

    In plain wordsIn diabetic rats, a sponge that slowly releases Tβ4 clearly increased the density of new blood vessels in wounds.

    Outcome
    IncreaseNew vessel density in wound
    Study

    ratn: not reported in source

    STZ-induced diabetic rats with hindlimb ischemia
    Outcome group
    Wound healing · Skin and wound

    Source sentences

    Summary
    Significant increases in CD31-positive endothelial cells and new vessel density were also observed.
    1 context sentence
    Summary · context
    This study investigates the possible use of a collagen-chitosan sponge scaffold encapsulated with thymosin beta 4 (CCSS-eTβ4), an angiogenic factor, to accelerate cutaneous wound healing in streptozotocin (STZ)-induced diabetic rats with hindlimb ischemia.

    In this study, Thymosin beta-4 (human) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Thymosin beta-4 (human).

  8. 11LabNot a test of Thymosin beta-4 (human) aloneIn vitro (cell-free)Pharmacokinetics

    The collagen-chitosan scaffold released Tβ4 in a controlled way, giving localized and prolonged effects over 12 days by ELISA.

    In plain wordsIn lab tests, the scaffold released Tβ4 slowly over 12 days.

    Outcome
    Not applicableControlled release of Tβ4 from scaffold
    Study

    n: not reported in source

    Collagen-chitosan sponge scaffold
    Outcome group
    Pharmacokinetics · Pharmacology

    Source sentences

    Summary
    The controlled release of Tβ4 from the scaffolds elicited localized and prolonged effects over 12 days, as shown by an enzyme-linked immunosorbent assay (ELISA).
    1 context sentence
    Summary · context
    This study investigates the possible use of a collagen-chitosan sponge scaffold encapsulated with thymosin beta 4 (CCSS-eTβ4), an angiogenic factor, to accelerate cutaneous wound healing in streptozotocin (STZ)-induced diabetic rats with hindlimb ischemia.

    In this study, Thymosin beta-4 (human) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Thymosin beta-4 (human).

AI wrote and checked these results. AI can make mistakes, so check important results against the source.

Version history

PepBank keeps every version of the data on this study. Status changes from Retraction Watch, Europe PMC and Crossref are listed with their source.

  1. Version 2Current

    13 Oct 2026, 01:52 UTC

    Study results updated

  2. Version 1

    12 Oct 2026, 18:17 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

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