Effects of Human Mesenchymal Stem Cells Coculture on Calcium-Induced Differentiation of Normal Human Keratinocytes

Author:

Sah Shyam Kishor1,Kim Hae Young1,Lee Ji Hae2,Lee Seong-Wook3,Kim Hyung-Sik4,Kim Yeon-Soo5,Kang Kyung-Sun6,Kim Tae-Yoon1ORCID

Affiliation:

1. a Laboratory of Dermatology-Immunology, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea

2. b Department of Dermatology, The Catholic University of Korea, St. Vincent's Hospital, Jungbu-daero, Paldal-gu, Suwon-si, Gyeonggi-do, Republic of Korea

3. c Department of Integrated Life Sciences, Dankook University, Jukjeon-ro, Suji-gu, Yongin, Republic of Korea

4. d Biomedical Research Institute, Pusan National University, School of Medicine, Pusan National University Hospital, Busan, Republic of Korea

5. e Graduate School of New Drug Development, Chungnam National University, Republic of Korea

6. f Adult Stem Cell Research Center, College of Veterinary Medicine, Seoul National University, Seoul, Republic of Korea

Abstract

Abstract The influence of mesenchymal stem cells (MSCs) on keratinocytes in altered microenvironments is poorly understood. Here, we cocultured umbilical cord blood-derived MSCs with normal human epidermal keratinocytes to evaluate their paracrine effect in the presence of high extracellular calcium (Ca2+) concentration. High Ca2+ environment to keratinocytes can disrupt normal skin barrier function due to abnormal/premature differentiation of keratinocytes. Surprisingly, we found that MSCs suppress both proliferation and differentiation of keratinocytes under a high Ca2+ environment in transforming growth factors β1 (TGFβ1)-dependent manner. Furthermore, we determined that MSCs can regulate the mitogen-activated protein kinases, phosphatidylinositol 3-kinase/protein kinase B, and protein kinase C pathways in Ca2+-induced differentiated keratinocytes. Knockdown of TGFβ1 from MSCs results in decreased suppression of differentiation with significantly increased proliferation of keratinocytes compared with control MSCs. MSCs-derived TGFβ1 further induced growth inhibition of keratinocyte in high extracellular Ca2+ environment as analyzed by a decrease in DNA synthesis, accumulation of phosphorylated retinoblastoma protein, cdc2, and increased mRNA level of p21, and independent of TGFβ1/SMAD pathway. Taken together, we found that MSCs-derived TGFβ1 is a critical regulator of keratinocyte function, and involves multiple proximal signaling cascades.

Funder

Bio and Medical Technology Development Program, the National Research Foundation

Korean Government, the Republic of Korea, MSIP

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,Molecular Medicine

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